Patent Application
20180318428
The present invention, in some embodiments thereof, relates to therapy and, more particularly, but not exclusively, to novel functionalized PGA-based polymeric carriers and to uses thereof for conjugating thereto, and delivering, oligonucleotides, and in the treatment of medical conditions treatable by oligonucleotides, for example, medical conditions treatable by gene therapy such as gene silencing.
The gene silencing activity of small interfering RNAs (siRNAs) and microRNAs (miRNAs) has been recognized as an efficient strategy in therapy, due to their ability to knock-down the expression of disease-causing genes with a known sequence. Various medical applications to siRNA/miRNA have been suggested, including, for example, treatment of viral infections, neurodegenerative disorders and cancer. Increasing evidences point out to post-transcriptional gene silencing as a potential leading approach in cancer therapy.
siRNA and miRNA are short sequences of double-stranded RNA that reach the cell cytoplasm either by exogenous double-stranded RNA transfection or by processing of nuclear endogenous transcripts respectively. Both cases result in RNA interference (RNAi), which is the process of sequence-specific, post-transcriptional gene silencing following either RNA degradation or translation arrest.
The two separate mechanisms of action end up in a common pathway: cytoplasmic long dsRNA that was exogenously introduced is cleaved by the enzyme dicer to a 21-23 nucleotides sequence and incorporated into the RNA-induced silencing complex (RISC), where the sense strand is degraded. The anti-sense strand then leads the complex to the complementary mRNA and induces its degradation.
As shown therein, cytoplasmic long double-stranded RNAs are cleaved to siRNA by Dicer. Pri-miRNAs are transcribed in the nucleus, and are processed by Drosha to create pre-miRNAs which are transported to the cytoplasm. Pre-miRNAs are then cleaved by Dicer into mature miRNAs. Both mature miRNAs and siRNAs are incorporated into the RISC complex, that eliminates the sense strand and induce Watson-Crick base pairing (full or partial) with target mRNA. As a consequence gene silencing occurs either by mRNA degradation or by repression of the translation.
One difference between the two mechanisms is in the degree of complementation: while siRNA binds to only one perfect match and therefore can degrade only one mRNA specific sequence, miRNA recognizes partially complementary sequences, leading to arrest of translation of several mRNAs.
Research involving multiple human cancers has shown a connection between miRNA downregulation, tumorigenesis and poor cellular differentiation. Other studies have demonstrated the ability of exogenous synthetic miRNA/siRNA to reduce cell-viability in cancerous tissue cultures and to inhibit growth and metastasis of tumor xenografts in mice models.
The potential of silencing a specific oncogene for cancer therapy has been demonstrated by targeting vascular endothelial growth factor (VEGF). It has been shown that Chitosan-VEGF siRNA nanoplexes that were injected intratumoraly in a rat mammary cancer model resulted in a marked reduction in tumor growth [Salva, E., et al., Nucleic Acid Ther, 2012. 22(1): p. 40-8].
Other examples include cationic liposomes that were used to deliver miR-29b and miR-133b, which are potential tumor-suppressors and key regulators of CDK6, DNMT3B, and MCL1 to non-small cell lung cancer (NSCLC) cells. Successful delivery of those miRNAs significantly reduced cell growth both in vitro and in a xenograft murine model [Wu, Y., et al., Mol Ther Nucleic Acids, 2013. 2: p. e84; Wu, Y., et al., Mol Pharm, 2011. 8(4): p. 1381-9].
Another attempt to use a tumor-suppressor miRNA for cancer treatment is the ongoing phase I study with miR-34a (MRX34), which is given intravenously to patients with unresectable primary liver cancer or metastatic cancer with liver involvement (see, www.clinicaltrials(dot)gov/ct2/show/NCT01829971). miR-34a is a transcriptional target of p53 that was found to down regulate MYCN, BCL2, SIRT1, SFRP1, CAMTA1, NOTCH1, JAG1, CCND1, CDK6, and E2F3, and its expression resulted in a reduction of cellular proliferation, metastasis and resistance to chemotherapy [Zenz, T., et al., Blood, 2009. 113(16): p. 3801-8; Hermeking, H., Cell Death Differ, 2010. 17(2): p. 193-9].
SiRNAs/miRNAs gene silencing-based therapeutic approaches have encountered pharmacokinetic limitations. Injectable RNAi therapeutics (parenteral administration) have faced fundamental delivery problems including aggregation in aqueous media, very short in vivo circulation time (ti/2 ranging from seconds to minutes), fast renal clearance, high immunogenicity and non-specific body distribution. For both locally administered as well as parenteral therapeutics, additional drawbacks include poor intracellular uptake (due to its high molecular weight and negative charge), poor ability to escape from the endosome and the need for cytoplasmic localization in order for the siRNA/miRNA to be active.
In order to increase the in vivo stability of the siRNA/miRNA, chemical modifications have been introduced on the oligonucleotides backbone. These include mainly 2′F, 2′O-Me and 2′H substitutions that were found to reduce cytokines production and to increase stability and specificity [Kenski, D. M., et al., Mol Ther Nucleic Acids, 2012. 1: p. e5; Esau, C. C., 2008. 44(1): p. 55-60; C. C. Esau, Inhibition of microRNA with antisense oligonucleotides. Methods 44, 55-60 (2008); published online EpubJan (10.1016/j.ymeth.2007.11.001)].
Several non-viral RNA delivery approaches have been developed, most being based on cationic lipids or polymeric carriers that can electrostatically interact with the negatively-charged RNA [Wu et al., 2011 (supra); Ofek, P., et al., FASEB J, 2010. 24(9): p. 3122-34; Basha, G., et al., Mol Ther, 2011. 19(12): p. 2186-200]. Most delivery systems are based upon electrostatic interactions between positively charged polymers, dendrimers or liposomes and the negatively charged siRNA. The resulting supramolecular structure forms polyplexes or lipoplexes. Other methods include encapsulation into the core of a nanoparticle, or chemical conjugation to a polymer.
The different structures such as linear, branched or globular, can form different assemblies when bound to the RNA such as RNAi entrapped in liposomes, core and shell particles, and polyplexes where the RNAi is complexed with polymers.
Several studies use conjugation of RNAi to a polymeric chain or the combination of RNAi conjugation with its subsequent assembly into supramolecular structures. See, Tiram, G., et al., Journal of Biomedical Nanotechnology, 2014. 10: p. 50-66, Ofek et al., 2010 (supra); McCaskill, J., et al., Mol Ther Nucleic Acids, 2013. 2: p. e96; Shi, J., et al., Angew Chem Int Ed Engl, 2011. 50(31): p. 7027-31; York, A. W., F. Huang, and C. L. McCormick, Biomacromolecules, 2010, 11(2): p. 505-14; and Jeong, J. H., et al., Bioconjug Chem, 2009. 20(1): p. 5-14. Some examples include CALAA-01, a nano-sized cyclodextrin based siRNA-delivery system consisting of a mixture with siRNA and adamantane-coupled PEG stabilizers some of which carry a transferrin transferrin ligand. This delivery system targets RRM2, a gene involved in DNA replication; and Dynamic PolyConjugates (DPC), which is a polymer functionalized with N-acetyl-galactosamine (NAG) ligand for hepatocyte targeting and linked to siRNA with a disulfide bond for reductive release [Rozema et al. (2007) Proc Natl Acad Sci USA, 104, 12982-7]. The basis of the system is an endosomolytic backbone that is reversibly masked with PEG and the targeting moiety, but once in the endosome, goes through selective activation at the acidic environment, to release its cargo to the cytoplasm.
Polymer therapeutics can address many of the problems arisen by the administration of naked siRNA/miRNA. In the case of polymer-RNAi polyplexes, the RNAi can be electrostatically bound to proteins, polysaccharides, or synthetic polymers. Normally, polymer-RNAi polyplexes achieve tumor specific targeting by the enhanced permeability and retention (EPR) effect. The impaired hyperpermeable angiogenic tumor vessels allow preferential extravasation of circulating macromolecules, and once in tumor interstitium, they are retained there by poor intra-tumoral lymphatic drainage [Maeda et al., J Control Release 65, 271-284 (2000); R. Satchi-Fainaro et al., in Polymer therapeutics II: Polymers as drugs, Conjugates and Gene Delivery Systems, R. Satchi-Fainaro, R. Duncan, Eds. (Springer, 2006), vol. 193, pp. 1-65]. In order to improve targeting specificity, the polymer can be conjugated to a moiety of interest, for example antibodies, peptides or sugars which target disease-related antigens or receptors [A. Nori and J. Kopecek, Adv Drug Deliv Rev 57, 609-636 (2005)]. In order to ensure cytoplasmic localization, polyaminated polymers are used as proton sponges: a large number of weak conjugate bases (with buffering capabilities at pH 5-6), lead to proton absorption in acid organelles and the consequent osmotic pressure across the organelle membrane. That further causes swelling and burst of the acidic compartments and release of their contents to the cytoplasm [M. V. Yezhelyev et al. Journal of the American Chemical Society 130, 9006-9012 (2008); Boussif et al. Proceedings of the National Academy of Sciences of the United States of America 92, 7297-7301 (1995)].
Poly(α)glutamic acid is a synthetic polymer, which is non-immunogenic, non-toxic, and biodegradable by cathepsin B, an enzyme that is highly expressed in most tumor tissues. PGA was shown to be safe at the required doses in clinical trials, when bound to the chemotherapeutic drug Paclitaxel. PGA is composed of naturally-occurring L-glutamic acid linked together through amide bonds rather than non-degradable C—C backbone. PGA is usually prepared from poly(γ-benzyl-L-glutamate) by removing the benzyl protecting group with the use of hydrogen bromide.
A sequential copolymer of protected PGA may be synthesized by peptide coupling reactions. For the preparation of high-molecular-weight homopolymers and block or random copolymers of protected PGA, tri-ethylamine-initiated polymerization of the N-carboxyanhydride (NCA) of γ-benzyl-L-glutamate is the most frequently used method [Pan, H. and Kopecek, J., Multifunctional Water-Soluble Polymers for Drug Delivery, in Multifunctional Pharmaceutical Nanocarriers, M. Ferrari, Editor 2008, Springer. p. 81-142].
Additional background art includes JP Patent No. JP 59071690; WO 2012/051459; WO 2012/051458; WO 2012/051457; U.S. Patent Application Publication No. 2012/0093762; Zhao et al., Biomacromolecules 2013, 14, 1777-1786; and ISSN:0365-088X.
The present inventors have now devised and successfully prepared, characterized and practiced, novel delivery vehicles for transporting oligonucleotides to cells. The present inventors have contemplated utilizing the pendant free γ-carboxyl group in the repeating L-glutamic acid units in PGA for providing functionality for attachment of various amine-containing units, to which RNA can be associated.
The delivery vehicles described herein include PGA-based polymers and co-polymers, featuring side chains (pendant groups) terminating with various amine-containing moieties.
According to an aspect of some embodiments of the present invention there is provided a polymeric compound, also referred to herein interchangeably as a polymer, composed of a plurality of BU(1), a plurality of BU(2), a plurality of BU(3), a plurality of BU(4), a plurality of BU(5), a plurality of BU(6), a plurality of BU(7) and/or a plurality of BU(8), as described herein. According to another aspect of some embodiments of the present invention there is provided a conjugate comprising a polymer as described herein in any of the respective embodiments, being in association with an oligonucleotide.
According to an aspect of some embodiments of the present invention there is provided a polymer represented by Formula I*:
wherein:
x, y, z, u, v and w each independently represents the mol % of the respective backbone unit, such that x+y+z+u+v+w=100 mol %, wherein x+y+z+u+v≥40 mol %;
Ra is an N-terminus group;
Rb is a C-terminus group;
L1, L2, L3 and L6 is each independently a linear (non-branched) linking moiety;
L4 and L5 are each independently a branched linking moiety;
R1-R11 are each independently selected from H, alkyl and cycloalkyl; and
Z is a nitrogen-containing heterocyclic moiety,
provided that at least one of x, y and z is other than 0,
and provided that:
(i) x is at least 40 mol %, y is lower than 40 mol %, and at least one of R1 and R2 is other than H; or
(ii) when u is other than 0, at least one of R9 and R10 is an alkyl being more than 3 carbon atoms in length, and at least one of x, y, z and v is other than 0; or
(iii) when v is other than 0, u is other 0; or
(iii) z is greater than 40 mol %.
According to some of any of the embodiments described herein, x ranges from 50 to 100 mol %, or from 60 to 100 mol %, or from 70 to 100 mol %.
According to some of any of the embodiments described herein, each of R1 and R2 is alkyl.
According to some of any of the embodiments described herein, the alkyl is methyl.
According to some of any of the embodiments described herein, R3 and R4 are each H.
According to some of any of the embodiments described herein, u is at least 40 mol %.
According to some of any of the embodiments described herein, u ranges from 40 to 50 mol %.
According to some of any of the embodiments described herein, y is other than 0.
According to some of any of the embodiments described herein, y ranges from 60 to 50 mol % respectively.
According to some of any of the embodiments described herein, R9 is H and R10 is the alkyl.
According to some of any of the embodiments described herein, each of R9 and R10 is the alkyl.
According to some of any of the embodiments described herein, the alkyl is 5 to 10, or 5 to 8, or 6 to 8, carbon atoms in length.
According to some of any of the embodiments described herein, v is at least 20, or at least 30 mol %.
According to some of any of the embodiments described herein, v is other than 0 and u is at least 20, or at least 30 mol %.
According to some of any of the embodiments described herein, v is other than 0, and at least one of x, y and z is other than 0.
According to some of any of the embodiments described herein, y is other than 0.
According to some of any of the embodiments described herein, y ranges from 40 to 60 mol %.
According to some of any of the embodiments described herein, Z is a nitrogen-containing heteroaryl.
According to some of any of the embodiments described herein, the linear linking moiety is a substituted or unsubstituted alkylene.
According to some of any of the embodiments described herein, the branched linking moiety is Rc-CRd-Rf, wherein Rd is H or alkyl; and Rc and Rf are each independently an alkylene or absent.
According to some of any of the embodiments described herein, the polymer is selected from Polymer F, Polymer I, Polymer K, Polymer M, Polymer O, Polymer P, and Polymer T, as described herein.
According to an aspect of some embodiments of the present invention there is provided a polymer represented by Formula II:
wherein:
Q1 and Q4 are each independently selected from an N-terminus group, and a polymeric chain comprising a plurality of one or more of BU(1), BU(2), BU(3), BU(4), BU(5), BU(6) and BU(7) backbone units; and
Q2 and Q3 are each independently selected from an C-terminus group and a polymeric chain comprising a plurality of one or more of BU(1), BU(2), BU(3), BU(4), BU(5), BU(6) and BU(7) backbone units, as described herein in any of the respective embodiments and any combination thereof, provided that at least one of Q1, Q2, Q3 and Q4 comprises a plurality of one or more of BU(2), BU(3), BU(4), and BU(6) backbone units.
According to some of any of the embodiments described herein, a total mol % of the BU(2), BU(3), BU(4), and BU(6) backbone units in the Q1, Q2, Q3 and/or Q4 is at least 40%.
According to some of any of the embodiments described herein, a mol % of the BU(8) ranges from 1 to 20%.
According to an aspect of some embodiments of the present invention there is provided a polymer comprising a plurality of backbone units selected from BU(1), BU(2), BU(3), BU(4), BU(5), and/or BU(6), and a plurality of BU(7) backbone units, as described herein in any of the respective embodiments and any combination thereof, provided that at least 40 mol % of the backbone units are selected from BU(2), BU(3), BU(4), and/or BU(6).
According to some of any of the embodiments described herein, the polymer is arranged as a block-copolymer comprising at least one block comprising a plurality of BU(1), BU(2), BU(3), BU(4), BU(5), and/or BU(6), and at least one block comprising the BU(7) backbone units.
According to some of any of the embodiments described herein, a total mol % of the BU(2), BU(3), BU(4), BU(5), and/or BU(6) is at least 60%.
According to some of any of the embodiments described herein, a polymer as described herein in any of the respective embodiments and any combination thereof is for associating therewith an oligonucleotide.
According to some of any of the embodiments described herein, a polymer as described herein in any of the respective embodiments and any combination thereof is for delivering the oligonucleotide to a cell.
According to some of any of the embodiments described herein, a polymer as described herein in any of the respective embodiments and any combination thereof, when in association with the oligonucleotide, for transfecting a cell.
According to an aspect of some embodiments of the present invention there is provided a conjugate (polyplex) comprising the polymer as described herein in any of the respective embodiments and any combination thereof and an oligonucleotide associated therewith.
According to some of any of the embodiments described herein, the oligonucleotide is associated with the polymer via electrostatic interactions.
According to some of any of the embodiments described herein, the electrostatic interactions are between terminal amine groups of the polymer and phosphate groups of the oligonucleotide.
According to some of any of the embodiments described herein, a ratio between a number of the terminal amine groups and a number of the phosphate groups ranges from 15:1 to 1:1, or from 10:1 to 1:1, or from 5:1 to 1:1.
According to some of any of the embodiments described herein, the oligonucleotide is an RNA oligonucleotide.
According to some of any of the embodiments described herein, the RNA oligonucleotide is selected from a messenger RNA (mRNA), a micro RNA (miRNA), a small interfering RNA (siRNA) and a tiny noncoding RNA (tnRNA).
According to an aspect of some embodiments of the present invention there is provided a conjugate as described herein in any of the respective embodiments and any combination thereof for delivering the oligonucleotide into a cell.
According to an aspect of some embodiments of the present invention there is provided a conjugate as described herein in any of the respective embodiments and any combination thereof for use in transfecting a cell.
According to an aspect of some embodiments of the present invention there is provided a conjugate as described herein in any of the respective embodiments and any combination thereof for use in gene therapy or in gene silencing, or for use in the manufacturing of a medicament for use in gene therapy or gene silencing, or for treating medical conditions in which gene therapy or gene silencing is beneficial.
According to an aspect of some embodiments of the present invention there is provided a pharmaceutical composition comprising the conjugate as described herein in any of the respective embodiments and any combination thereof and a pharmaceutically acceptable carrier.
According to some of any of the embodiments described herein, the carrier is an aqueous carrier.
According to some of any of the embodiments described herein, the carrier further comprises a dispersing agent.
According to some of any of the embodiments described herein, the conjugate is in a form of a plurality of particles dispersed in the carrier.
According to some of any of the embodiments described herein, an average particle size (diameter) of the particles is lower than 1 micron, or lower than 500 nm or lower than 300 nm, or lower than 200 nm.
According to some of any of the embodiments described herein, the PDI of the particles is lower than 1, or lower than 0.5, or lower than 0.3.
According to an aspect of some embodiments of the present invention there is provided a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a conjugate which comprises a polymer represented by Formula I, as described herein in any of the respective embodiments and any combination thereof.
According to some of any of the embodiments described herein, the carrier further comprises a surfactant.
According to some of any of the embodiments described herein, the composition is prepared by means of a microfluidic system.
According to some of any of the embodiments described herein, the carrier comprises a polyethyleneglycol (PEG).
According to some of any of the embodiments described herein, the polymer is selected from Polymers A-Y, as described herein.
According to some of any of the embodiments described herein, the polymer is selected from Polymer A, Polymer B, Polymer F, Polymer I, Polymer K, Polymer M, Polymer O, Polymer P, and Polymer T.
According to some of any of the embodiments described herein, the carrier is an aqueous carrier.
According to some of any of the embodiments described herein, the carrier comprises glucose.
According to some of any of the embodiments described herein, the oligonucleotide is associated with the polymer via electrostatic interactions.
According to some of any of the embodiments described herein, the oligonucleotide is an RNA oligonucleotide, as described herein.
According to some of any of the embodiments described herein, the composition is for delivering the oligonucleotide into a cell.
According to some of any of the embodiments described herein, the composition is for transfecting a cell.
According to some of any of the embodiments described herein, the composition is for use in gene therapy or in gene silencing.
Unless otherwise defined, all technical and/or scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the invention pertains. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of embodiments of the invention, exemplary methods and/or materials are described below. In case of conflict, the patent specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and are not intended to be necessarily limiting.
Some embodiments of the invention are herein described, by way of example only, with reference to the accompanying drawings and tables. With specific reference now to the drawings in detail, it is stressed that the particulars shown are by way of example and for purposes of illustrative discussion of embodiments of the invention. In this regard, the description taken with the drawings makes apparent to those skilled in the art how embodiments of the invention may be practiced.
In the drawings:
The present invention, in some embodiments thereof, relates to therapy and, more particularly, but not exclusively, to novel functionalized PGA-based polymeric carriers and to uses thereof for conjugating thereto and delivering oligonucleotides, and in the treatment of medical conditions treatable by oligonucleotides, for example, medical conditions treatable by gene therapy such as gene silencing.
Before explaining at least one embodiment of the invention in detail, it is to be understood that the invention is not necessarily limited in its application to the details set forth in the following description or exemplified by the Examples. The invention is capable of other embodiments or of being practiced or carried out in various ways.
Currently available delivery vehicles for siRNA/miRNA offer only partial solutions. Up to date, several technologies have been tested, yet none has shown suitable safety profile and none is targeted to pathological tissue. These technologies rely on the passive accumulation by the EPR effect or on a default hepatic accumulation following systemic administration.
The present inventors have contemplated that electrostatic-based complexation between polyaminated-PGA and modified siRNA or miRNA will form therapeutically active nano-scaled polyplexes that will introduce the following list of benefits: (i) Increased stability in plasma; (ii) Specific delivery to the tumor site and accumulation of the siRNA or miRNA in the angiogenic tissue (e.g. tumor vascular bed); (iii) cellular uptake and endosomal escape that will lead the siRNA/miRNA to its active site—the mRNA in the cytoplasm; (iv) biodegradability of the polymeric backbone by cathepsin B; and (v) Prolongation of the circulating half-life of the polyplexes compared with the free siRNA/miRNA.
The present inventors have contemplated utilizing the pendant free γ-carboxyl group in the repeating L-glutamic acid units in PGA for providing functionality for attachment of various amine-containing units, to which RNA can bind by electrostatic interactions. Poly-aminated PGA is positively charged, thus can internalize to the target cell via electrostatic attraction to the negatively-charged cell membrane and provide for efficient endosomal escape via proton sponge effect.
Thus, according to some embodiments of the present invention, a polymeric delivery vehicle that interacts electrostatically with oligonucleotides such as siRNA or miRNA is provided. Targeted tumor accumulation is achieved by the Enhanced Permeability and Retention (EPR) effect—the leakiness of the tumor blood vessels that allows extravasation of nanometric macromolecules. In addition, for overcoming obstacles such as plasma aggregation and high immunogenicity, the polymer is also designed to permeate through the cell membrane via the endosome and transfer to the cytoplasm, its site of action. The polymer is degraded at the lysosome by cathepsin B which is prevalent in tumors.
The present inventors have designed, synthesized and characterized various polyaminated polyglutamic acid polymers that formed complexes with siRNA and miRNA.
Properties such as strength of complexation between the polymer and siRNA, size and charge of polyplexes, their cellular internalization, silencing activity and toxicity were investigated so as to identify advantageous modifications of the PGA pendant groups. The present inventors have identified several structural features which provide such polymers with improved capability to complex thereto and deliver siRNA and/or miRNA to the cytoplasm, compared to other polyaminated polyglutamic acid-based polymers.
The present inventors have further designed a formulation comprising the conjugates of these polyaminated polyglutamic acid polymers with ribonuclear oligonucleotides (polyplexes), while maintaining the polyplexes as discrete nanoparticles within the solution and while maintaining, and even improving, the therapeutic effect thereof.
Some embodiments of the present invention therefore relate to a polyaminated α-Poly-L-glutamic acid-based delivery system, for targeted delivery of oligonucleotides, and to polyplexes formed by associating, e.g., via electrostatic interactions, the positively charged amine moieties of the aminated PGA polymers and negatively charged oligonucleotides.
The polymer-oligonucleotide polyplexes described herein represent a novel and promising approach for tumor targeted delivery of oligonucleotides such as siRNA/miRNA. The biodegradability, non-immunogenicity and high versatility of PGA makes it an attractive carrier candidate to improve the ability of e.g., siRNA/miRNA to accumulate in the tumor environment, cross the cell membrane and exert its biological effect in a highly efficient and specific manner.
These polyplexes can be selectively activated in tumor sites due to their biodegradability by cathepsin B, an over-expressed enzyme in lysosomes of several types of tumor cells, in tumor endothelial cells and in the tumor extracellular matrix (ECM).
The polymeric delivery system described herein can be utilized therapeutically to treat all pathologies characterized by impaired siRNA or miRNA genetic regulation such as, but not limited to, cancer, viral diseases, cardiovascular diseases, metabolic diseases and neurodegenerative diseases. In addition, the polymeric delivery system can be utilized as a transfection reagent for laboratory research use.
Referring now to the drawings
According to an aspect of some embodiments of the present invention there is provided a polymeric compound, also referred to herein interchangeably as a polymer, as described herein.
According to an aspect of some embodiments of the present invention there is provided a polymeric compound, also referred to herein interchangeably as a polymer, represented by Formula I as described herein.
According to an aspect of some embodiments of the present invention there is provided a polymeric compound, also referred to herein interchangeably as a polymer, represented by Formula Ia, Ib or Ic, as described herein.
According to an aspect of some embodiments of the present invention there is provided a polymeric compound, also referred to herein interchangeably as a polymer, represented by Formula II as described herein.
According to an aspect of some embodiments of the present invention there is provided a polymeric compound, also referred to herein interchangeably as a polymer, represented by Formula III as described herein.
According to an aspect of some embodiments of the present invention there is provided a polymeric compound, also referred to herein interchangeably as a polymer, composed of a plurality of BU(1), a plurality of BU(2), a plurality of BU(3), a plurality of BU(4), a plurality of BU(5), a plurality of BU(6), a plurality of BU(7) and/or a plurality of BU(8), as described herein. According to another aspect of some embodiments of the present invention there is provided a conjugate comprising a polymer as described herein in any of the respective embodiments, being in association with an oligonucleotide.
According to another aspect of some embodiments of the present invention, there is provided a pharmaceutical composition comprising a conjugate as described herein and a pharmaceutically acceptable carrier.
According to another aspect of some embodiments of the present invention, the conjugates, or compositions comprising same, as described herein, are used for delivering the oligonucleotides into cells, for transfecting cells, and/or in gene therapy, particularly gene silencing, as described herein.
Herein, the term “conjugate” describes a chemical entity in which two or more moieties (e.g., the polymer and the oligonucleotide) are associated to one another, as defined herein. In some embodiments, the association is via electrostatic interactions, as defined herein. In some embodiments, the electrostatic interactions are between phosphate groups of the oligonucleotide and terminal amine groups of pendant groups of the polymer.
A conjugate as described herein is also referred to herein throughout as a “polyplex”.
The Polymer:
Herein throughout, the term “polymer” is also referred to herein as “polymeric compound” and describes an organic substance composed of a plurality of repeating structural units covalently connected to one another.
The repeating structural units are backbone units, which are covalently linked to one another to thereby form the polymeric backbone. The term “backbone units” is used herein to describe the portion of corresponding monomers upon polymerizing or co-polymerizing the monomers.
The term “polymer” as used herein encompasses a homopolymer, a copolymer and a mixture thereof (a blend). The term “homopolymer” as used herein describes a polymer that is made up of one type of monomers and hence is composed of homogenic backbone units. The term “copolymer” as used herein describes a polymer that is made up of more than one type of monomers and hence is composed of heterogenic backbone units.
In some embodiments, the polymer (or co-polymer) has an average molecular weight in the range of 100 Da to 800 kDa. In some embodiments, the polymer has an average molecular weight lower than 100 kDa or lower than 60 kDa. In some embodiments, the polymer's average molecular weight range is 10 kDa to 40 kDa.
Polymeric substances that have a molecular weight higher than 10 kDa typically exhibit an EPR effect, as described herein, while polymeric substances that have a molecular weight of 100 kDa and higher have relatively long half-lives in plasma and an inefficient renal clearance. Accordingly, a molecular weight of a polymeric conjugate can be determined while considering the half-life in plasma, the renal clearance, and the accumulation in the tumor of the conjugate.
According to some embodiments, the polymer comprises backbone units that form a polymeric backbone of polyglutamic acid (PGA). Such polymers are also referred to herein as polymers or co-polymers deriving from PGA, or PGA-based polymers, and comprise backbone units derivable from glutamic acid.
PGA contains carboxylic functional groups as its side chains (pendant groups). PGA can be readily degraded by lysosomal enzymes such as Cathepsin B, to its nontoxic basic components, L-glutamic acid, D-glutamic acid and/or D,L-glutamic acid.
As used herein, a polyglutamic acid encompasses poly(L-glutamic acid), poly(D-glutamic acid), poly(D,L-glutamic acid), poly(L-gamma glutamic acid), poly(D-gamma glutamic acid) and poly(D,L-gamma glutamic acid). Accordingly, PGA-based polymers or copolymers can comprise backbone units derivable from D-glutamic acid, L-glutamic acid, a racemic mixture of D- and L-glutamic acid, L-gamma glutamic acid, D-gamma glutamic acid and racemic mixture of D- and L gamma glutamic acid.
In some embodiments, the PGA-based polymers or co-polymers described herein comprise at least 50% of its backbone units as derivable from glutamic acid, and optionally comprises 60, 70, 80, 90 or 100% of its backbone units as derivable from glutamic acid.
According to some embodiments, the polymer is a co-polymer that comprises a plurality of backbone units that form a polymeric backbone of polyglutamic acid (PGA), referred to herein as PGA backbone units, and a plurality of other backbone units. The other backbone units can be interlaced, or interrupt, the polymeric backbone formed of the PGA backbone units, to form a heterogenic polymeric backbone. Alternatively, the other backbone units can be included in the polymeric backbone so as to form a block co-polymer, composed of one or more polymeric backbone formed of the PGA backbone units and one or more polymeric backbones forms of the other backbone units, whereby these polymeric backbones are attached to one another alternately, in any order. Further alternatively, or in addition to any of the foregoing, the other backbone units cross-link one or more polymeric backbone units formed of the PGA backbone units.
According to the present embodiments, at least a portion of the backbone units in the polymer or co-polymer as described herein are further substituted so as to feature one or more terminal amine groups, for forming an association with an oligonucleotide, as described herein. Those backbone units that are not further substituted so as to feature an amine group are referred to herein as “free” backbone units.
A PGA-based polymers or co-polymer as described herein, in which a portion of the PGA backbone units is substituted so as to feature an amine terminal group is also referred to herein interchangeably as “PGAamine polymer”, “aminated PGA polymer”, “PGA-based polymer”, PGA aminated derivative, PGA amination derivative and simply “polymer” or “polymeric compound”.
Polymers according to embodiments of the present invention comprise a plurality of backbone units covalently linked to one another, whereby the backbone units are selected from the backbone units denoted herein as BU(1), BU(2), BU(4), BU(5), BU(6), BU(7) and BU(8), as follows, provided that at least 40% of the backbone units are one or more of BU(2), BU(4), BU(5) and BU(6).
wherein:
L1, L2, L3, L6 and L8 is each independently a linear linking moiety;
L4 is a branched linking moiety;
L5 is a linear or branched linking moiety, or is absent (depending on the nature of R9 and R10, as described in further detail hereinunder);
L7 is a linear or branched linking moiety, or is absent (depending on the nature of R9 and R10, as described in further detail hereinunder);
R1-R13 are each independently selected from H, alkyl and cycloalkyl; and
Z is a nitrogen-containing heterocyclic moiety.
In some embodiments, the backbone units forming a polymeric compound as described herein are covalently linked to one another so as to form a peptide (amide) bond. The backbone units forming a polymeric compound as described herein are covalently linked to one another in any order, unless indicated otherwise.
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of two of the backbone units BU(1), BU(2), BU(4), BU(5), BU(6), BU(7) and BU(8) as described herein.
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of three of the backbone units BU(1), BU(2), BU(4), BU(5), BU(6), BU(7) and BU(8) as described herein.
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of four of the backbone units BU(1), BU(2), BU(4), BU(5), BU(6), BU(7) and BU(8) as described herein.
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of five of the backbone units BU(1), BU(2), BU(4), BU(5), BU(6), BU(7) and BU(8) as described herein.
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of six of the backbone units BU(1), BU(2), BU(4), BU(5), BU(6), BU(7) and BU(8) as described herein.
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of seven of the backbone units BU(1), BU(2), BU(4), BU(5), BU(6), BU(7) and BU(8) as described herein.
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of all of the backbone units BU(1), BU(2), BU(4), BU(5), BU(6), BU(7) and BU(8) as described herein.
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(1) and one or more of BU(2), BU(4), BU(5) and BU(6).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(3) and one or more of BU(1), BU(2), BU(4), BU(5) and BU(6).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(3) and BU(1).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units consisting of BU(3).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(3) and one or more of BU(2), BU(4), BU(5) and BU(6).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(2) and BU(3).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(3) and BU(5).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(3) and BU(6).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(3), BU(5) and BU(6).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(2) and BU(5).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(2), BU(3) and BU(5).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(3) and BU(7).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(7) and one or more of BU(2), BU(3), BU(4), BU(5) and BU(6).
In some embodiments, a polymeric compound as described herein comprises a plurality of backbone units composed of BU(8) and one or more of BU(2), BU(3), BU(4), BU(5) and BU(6).
In some of any of the embodiments described herein, R11 is H and BU(1) represents “free” backbone units of PGA.
Herein throughout, a “linear linking moiety” describes a bi-radical linear, preferably aliphatic, group. By “bi-radical” it is meant that the linking moiety has two attachment points such that it links between two atoms or two groups. In some embodiments, the linear linking moiety is or comprises a bi-radical hydrocarbon.
By “hydrocarbon” it is meant a moiety formed of a chain of carbon atoms covalently linked to one another, and substituted mainly by hydrogen atoms. A hydrocarbon can include, for example, one or more alkyl groups, one or more alkenyl groups, one or more alkynyl groups, one or more cycloalkyl groups and/or one or more aryl groups, on any order. Preferably, the hydrocarbon includes one or more aliphatic moieties, namely, one or more alkyl groups, one or more alkenyl groups and/or one or more alkynyl groups, and, depending on the moieties forming the hydrocarbon, it is saturated or unsaturated.
In some embodiments, the hydrocarbon comprises 1 to 10 carbon atoms, preferably 2 to 10 carbon atoms, preferably 2 to 8 carbon atoms, preferably 2 to 6 carbon atoms, in its backbone chain.
The hydrocarbon, or the moieties forming the hydrocarbon, can be substituted or unsubstituted, and are preferably substituted.
In some embodiments, the hydrocarbon can be interrupted by one or more heteroatoms, such as O or S or an amine group, as described herein.
In some embodiments, the linear linking moiety is a hydrocarbon, and in some of these embodiments, the hydrocarbon is an alkyl group, preferably unsubstituted alkyl.
Herein, a bi-radical alkyl group is also referred to as alkylene.
In some embodiments, the linear linking moiety comprises one or more alkylene(s), interrupted by one or more heteroatoms such as O, S or an amine group.
In some embodiments, the linear linking moiety comprises one or more alkylene(s), interrupted by one or more amine group(s).
Hereinthroughout, a “branched linking moiety” describes a multi-radical, preferably aliphatic, group. By “multi-radical” it is meant that the linking moiety has more than two attachment points such that it links between three or more atoms or groups. In some embodiments, the branched linking moiety is or comprises a linear linking moiety as described herein in any of the respective embodiments, which is terminated by a branching unit that has at least two attachment points to two or more atoms or groups.
In some of any of the embodiments described herein, a branched linking moiety is or comprises a branching unit represented by (Rc-CbRd-Rf), wherein Rd is H or alkyl; and Rc and Rf are each independently an alkylene or absent. This branching unit has one attachment point at the carbon atom denoted as Cb, and additional two attachment points at the same carbon atom Cb (if Rc and Rf are absent),or one attachment point at the same carbon atom Cb and one at one of Rc and Rf (if one of Rc and Rf are absent), or three attachment points at the same carbon atom Cb (if both Rc and Rf are absent). In some embodiments, a branched linking moiety is a branching unit represented by (Rc-CbRd-Rf), such that Cb is further attached to the amide group of a respective backbone unit. In some embodiments, a branched linking moiety comprises a branching unit represented by (Rc-CbRd-Rf), and Cb is attached to the amide group is a respective backbone unit via a hydrocarbon as described herein in any of the respective embodiments in the context of a linear linking moiety.
In some of any of the embodiments described herein for BU(2), L1 and L2 are each independently an alkylene, and in some embodiments, an unsubstituted alkylene.
In some of these embodiments, the alkylene has from 2 to 10 carbon atoms, or from 2 to 8 carbon atoms, or from 2 to 6 carbon atoms, or from 2 to 4 carbon atoms.
In some embodiments of BU(2), L1 and L2 are each independently an unsubstituted ethylene (—CH2—CH2—) or an unsubstituted propylene (—CH2—CH2—CH2—). In some embodiments, L1 and L2 are each unsubstituted propylene (—CH2—CH2—CH2—).
In some of any of the embodiments described herein for BU(2), at least one of R1 and R2 is other than H, and in some embodiments each of R1 and R2 is other than H. In some embodiments, R1 and R2 are each independently an alkyl, preferably a short alkyl, having 1 to 6, preferably 1 to 4 carbon atoms. In some embodiments, R1 and R2 are each methyl.
In some of any of the embodiments described herein for BU(2), in at least a portion of the BU(2) units each of R1 and R2 is other than H, e.g., each is methyl, and each of L1 and L2 is an unsubstituted alkylene, e.g., an unsubstituted propylene.
In some of any of the embodiments described herein for BU(2), in at least a portion of the BU(2) units, each of R1 and R2 is H, and each of L1 and L2 is an unsubstituted alkylene, e.g., an unsubstituted ethylene.
When a polymeric compound comprises a plurality of BU(2) backbone units, the BU(2) units can be the same or different, as described in further detail hereinbelow. When different, the BU(2) units can differ from one another by one or more of L1 and L2 and/or by one or more of R1 and R2.
In some of any of the embodiments described herein for BU(3), L3 is a linear linking moiety as described herein in any of the respective embodiments. In some of any of the embodiments described herein for BU(3), L3 is an alkylene, and in some embodiments, an unsubstituted alkylene. In some of these embodiments, the alkylene has from 2 to 10 carbon atoms, or from 2 to 8 carbon atoms, or from 2 to 6 carbon atoms. In exemplary embodiments, L3 is an unsubstituted ethylene (—CH2—CH2—) or an unsubstituted propylene (—CH2—CH2—CH2—) or an unsubstituted hexylene —(CH2)6—.
In some of any of the embodiments of BU(3), at least one of R3 and R4 is H, and in some embodiments, R3 and R4 are each H.
In exemplary embodiments of BU(3), R3 and R4 are each H and L3 is an unsubstituted alkylene. In some of these embodiments, L3 is an unsubstituted ethylene. In some of these embodiments, L3 is an unsubstituted hexylene.
When a polymeric compound comprises a plurality of BU(3) backbone units, the BU(3) units can be the same or different, as described in further detail hereinbelow. When different, the BU(3) units can differ from one another by e.g., the length of L3 and/or by one or more of R3 and R4.
In some of any of the embodiments described herein for BU(4), L4 is a branched linking moiety as described herein in any of the respective embodiments. In some embodiments, L4 is a hydrocarbon terminating by a branching unit (Rc-CbRd-Rf) as described herein in any of the respective embodiments. In some of these embodiments, the hydrocarbon is an alkylene, and in some embodiments an unsubstituted alkylene. In some embodiments, the hydrocarbon is an alkylene (e.g., unsubstituted) of from 1 to 10, or from 1 to 8, or from 1 to 6, or from 1 to 4, or from 1 to 2, carbon atoms is length. In exemplary embodiments, the hydrocarbon is unsubstituted methylene or unsubstituted ethylene.
In some of any of these embodiments, Rd is H.
In some of any of these embodiments, Re and Rf are each independently an alkylene, and in some embodiments each is an unsubstituted alkylene. In some embodiments, Rc and Rf are each an unsubstituted alkylene of from 1 to 10, or from 1 to 8, or from 1 to 6, or from 1 to 4, or from 1 to 2, carbon atoms is length. In exemplary embodiments, Rc and Rf are each independently an unsubstituted methylene, an unsubstituted ethylene or an unsubstituted propylene. In exemplary embodiments, Rc and Rf are each an unsubstituted ethylene.
In exemplary embodiments, L4 is —(CH2)—CH[(CH2—CH2)—]2.
In some of any of the embodiments described herein for BU(4), R5, R6, R7 and R8 are each independently H or alkyl, preferably a short alkyl of 1 to 4 carbon atoms in length, preferably an unsubstituted alkyl, preferably unsubstituted methyl. In some embodiments, one or more of R5, R6, R7 and R8 is alkyl (e.g., methyl). In some embodiments, each of R5, R6, R7 and R8 is H.
When a polymeric compound comprises a plurality of BU(4) backbone units, the BU(4) units can be the same or different. When different, the BU(4) units can differ from one another by one or more of L4 and R5-R8.
In some of any of the embodiments described herein for BU(5), R9 is H and R10 is alkyl, preferably a linear (non-branched) alkyl. In some of these embodiments, L5 is absent. Alternatively, in some of these embodiments, L5 is a linear linking moiety as described herein in any of the respective embodiments, and in some of these embodiments, L5 is an alkylene, such that L5 and R10 together form a linear alkyl. Further alternatively, in some of these embodiments, L5 is a branched linking moiety which is Rc-CRd-Rf, Rc and Rf are absent, and L5 and R10 can be regarded as forming together a linear alkyl.
In some of any of these embodiments, the alkyl (e.g., R10, or an alkyl which L5 and R10 form together) is at least 5 atoms in length, and can be, for example, pentyl, hexyl, heptyl, or octyl, each being preferably unsubstituted.
In some of any of the embodiments described herein for BU(5), each of R9 and R10 is other than H, and in some of these embodiments each of R9 and R10 is alkyl, preferably an unsubstituted alkyl.
The alkyl according to some of these embodiments is preferably at least three carbon atoms in length, more preferably at least 5 carbon atoms in length, and can be, for example, from 3 to 10, or from 5 to 10, or from 5 to 8, or from 6 to 8, carbon atoms in length.
When each of R9 and R10 is other than H (e.g., alkyl, as described herein), L5 is a branched linking moiety, as described in any one of the respective embodiments and any combination thereof.
In some embodiments, the branched linking moiety is or comprises Rc-CRd-Rf, as described herein.
In some embodiments, the branched linking moiety is Rc-CRd-Rf, as described herein, such that L5 is Rc-CRd-Rf. In some of these embodiments, Rd is H.
In some embodiments, Rc and Rf are absent. In some of these embodiments of L5, Rd is H, and each of R9 and R10 is alkyl, such that L5, R9 and R10 can be regarded as forming together a branched alkyl. In some of these embodiments, each branch of the branched alkyl is at least 3 carbon atoms in length.
In some of any of embodiments described herein for BU(5), at least one of R9 and R10 is an alkyl being 3 or more, preferably 4 or more, carbon atoms in length.
When a polymeric compound comprises a plurality of BU(5) backbone units, the BU(5) units can be the same or different, as described in further detail hereinbelow. The BU(5) units can differ from one another by one or more of the length of an alkyl group (when formed of L5 and R10, wherein R9 is hydrogen and/or when R9 and R10 are each alkyl; the nature of R9 and R10 (being the same or different, or being one or two alkyls); and the length and/or nature of the linking moiety.
In some of any of the embodiments described herein for BU(6), L6 is an alkylene, preferably an unsubstituted alkylene, as described herein in any of the respective embodiments. In exemplary embodiments, L6 is unsubstituted ethylene.
By “nitrogen-containing heterocyclic moiety” are encompassed heteroalicyclic and heteroaryl moieties, as defined herein, containing one or more nitrogen atoms within the cyclic ring. When Z is a heteroaryl, preferably, at least one of the nitrogen atoms does not participate in the π-electron conjugation of the aromatic system. Exemplary nitrogen-containing heterocyclic moieties include, but are not limited to, imidazole, morpholine, piperidine, piperazine, oxalidine, pyrrole, oxazole, thiazole, pyrazole, pyridine, pyrimidine, quinoline, isoquinoline and purine. Preferred moieties, according to some embodiments, include, but are not limited to, imidazole, piperazine, piperidine, and pyridine.
In exemplary embodiments, L6 is ethylene and Z is imidazole.
When a polymeric compound comprises a plurality of BU(6) backbone units, the BU(6) units can be the same or different, as described in further detail hereinbelow. The BU(6) units can differ from one another by the L6 linking moiety (e.g., the length of an alkylene) and/or by the Z nitrogen-containing heterocyclic moiety.
According to some of any of the embodiments described herein for BU(7), one of R13 and R12 is hydrogen and one is other than hydrogen. In some of these embodiments, R13 is hydrogen and R12 is alkyl. In these embodiments, L7 is absent. Alternatively, L7 is a linear linking moiety, and in some embodiments it is an alkylene, as described herein. In these embodiments L7 and R12 form together a linear alkyl. The alkyl, according to these embodiments, is preferably of 2 to 10 carbon atoms in length, more preferably 2 to 8, or 2 to 6, or 2 to 4, carbon atoms in length.
In alternative embodiments, R12 and R13 are each independently an alkyl, and L7 is a branched linking moiety as described herein in any of the respective embodiments and any combination thereof. In some of these embodiments, L7 is Rc-CRd-Rf, Rd is H and Rc and Rf are absent. In some of these embodiments, R12 and R13 are each independently an alkyl of from 1 to 8 or from 1 to 6, or from 1 to 4 carbon atoms in length.
When a polymeric compound comprises a plurality of BU(7) backbone units, the BU(7) units can be the same or different. The BU(7) units can differ from one another by, for example, R12 and/or R13, and/or by L7.
According to some of any of the embodiments described herein, the BU(8) backbone units, when present, are cross-linked units, which cross-link polymeric chains in the polymeric compounds. These units can be interlaced, as single backbone units or as blocks (comprising a plurality of such units covalently attached to one another), between blocks composed of one or more of BU(2), BU(3), BU(4), BU(5), BU(6) and/or BU(7), according to the present embodiments.
The BU(8) units, when present, are covalently linked to at least two polymeric chains by means of two or more of the amine and carboxyl groups therein.
In some embodiments, when a BU(8) unit is included in the polymeric compound, the polymer can be represented by Formula II:
wherein:
Q1 and Q4 are each independently selected from an N-terminus group, as defined herein and a polymeric chain comprising a plurality of one or more of BU(1), BU(2), BU(3), BU(4), BU(5), BU(6) and BU(7) backbone units; and
Q2 and Q3 are each independently selected from an C-terminus group, as defined herein and a polymeric chain comprising a plurality of one or more of BU(1), BU(2), BU(3), BU(4), BU(5), BU(6) and BU(7) backbone units,
provided that at least one of Q1, Q2, Q3 and Q4 comprises a plurality of one or more of BU(2), BU(3), BU(4), and BU(6) backbone units.
In some of the embodiments of Formula II, at least one, at least two, at least three, or all of Q1, Q2, Q3 and Q4 comprises a plurality of BU(2) backbone units.
In some of any of the embodiments of BU(8), L8 is a linear (non-branched) linking moiety, as described herein in any of the respective embodiments. In some embodiments, L8 is or comprises a hydrocarbon, as described herein, interrupted by one or more heteroatoms, preferably one or more nitrogen atoms.
In exemplary embodiments, L8 is a hydrocarbon composed of alkylene and alkenylene groups, interrupted by one or more nitrogen atoms. In some embodiments, L8 is formed upon reacting two cross-linkable groups with a suitable bi-functional, cross-linking agent, and is the product of such a reaction. In exemplary embodiments, L8 is formed upon reacting aminoalkylene cross-linkable groups with a dialdehyde compound (e.g., glutaraldehyde), and as such, L8 is an alkylene chain interrupted by corresponding Schiff bases formed upon the cross-linking reaction. L8 can alternatively be an alkylene chain interrupted by any other moieties formed upon interaction between cross-linkable groups and a corresponding cross-linking agent or moieties. Additional, non-limiting examples of cross-linkable groups and cross-linking moieties formed therefrom include, disulfide bonds formed upon cross-linking thiolated amino acids such as, but not limited to, cysteine, cysteamine. Cross-linking agents or moieties that can be included for forming cross-links between amine and/or thiol groups include, but are not limited to, succinimidyl 3-(2-pyridyldithio)propionate), azide-phosphine crosslinkers; disuccinimidyl glutarate (DSG); Bis(sulfosuccinimidyl) suberat; click chemistry reagents; Genipin. Any other cross-linkable groups and corresponding cross-linking agents are contemplated for forming L8.
In some of any of the embodiments described herein, a polymeric compound as described herein can be regarded as featuring a peptide-like backbone chain, in which the backbone units are linked to one another via a peptide (amide) bond.
The groups at the N-terminus and at the C-terminus of such peptide-like backbone chain can be an amine, at the N-terminus, and hydroxy, at the C-terminus, reflecting the amine and carboxylic acid groups of the respective monomers used to form the polymeric backbone, and which are positioned at the N-terminus and the C-terminus of the polymeric compound, respectively.
In some embodiments, the N-terminus group is modified by replacing one or both hydrogens of the terminal amine by one or more substituents. Such substituents can be, for example, alkyl, cycloalkyl, aryl, acyl, carboxylate, as well as any of the substituents described in the context of an amide group hereinunder.
In exemplary embodiments, the N-terminus group is an amine in which one of the hydrogens is substituted by an alkyl. In some embodiments, the alkyl is at least 3, or at least 4 carbon atoms in length. In some embodiments, the alkyl is from 4 to 18 carbon atoms in length. The alkyl can be linear or branched alkyl, and is preferably a linear alkyl.
In some embodiments, the C-terminus group is modified by replacing the hydroxy group of the carboxylic acid by an alkoxy, aryloxy, alkyl, cycloalkyl, amine or a nitrogen-containing heterocyclic group, as these terms are defined herein, such that the modified C-terminus group is a carboxylate, a ketone, or an amide.
According to some of any of the embodiments described herein, and any combination thereof, a polymeric compound as described herein comprises a plurality of backbone units composed of one or more of BU(2), BU(3), BU(4) and BU(6), optionally in combination with backbone units BU(5) and/or BU(1).
Polymers according to embodiments of the present invention can be collectively represented by Formula I:
wherein:
x, y, z, u, v and w each independently represents the mol % of the respective backbone unit, such that x+y+z+u+v+w=100 mol %, wherein x+y+z+u+v≥40 mol %;
Ra is selected from hydrogen (in case an N-terminus group is amine) and alkyl, preferably an alkyl (linear or branched) of at least 4 carbon atoms in length, representing an alkyl substituent of an N-terminus amine, as described herein);
Rb is selected from hydroxyl (in case a C-terminus group is carboxylic acid), alkoxy (in case a C-terminus group is a carboxylate), amine (in case a C-terminus group is an amide) and pyrrolidinone (in case a C-terminus group is amide formed with a nitrogen-containing heterocyclic group);
R1-R11 are each independently selected from H, alkyl and cycloalkyl, as defined herein and as described in any one of the respective embodiments and any combination thereof;
L1, L2, L3 and L6 is each independently a linear (non-branched) linking moiety, as defined herein and as described in any one of the respective embodiments and any combination thereof;
L4 is a branched linking moiety, as defined herein and as described in any one of the respective embodiments and any combination thereof, for BU(4);
L5 is a linear linking moiety or a branched linking moiety, or is absent, as defined herein and as described in any one of the respective embodiments and any combination thereof, for BU(5); and
Z is a nitrogen-containing heterocylic moiety, as described in any one of the respective embodiments and any combination thereof, for BU(6),
provided that at least one of x, y and z is other than 0.
In some of any of the embodiments described herein, each of x, y, z, u and v, representing the mol % of BU(2), BU(3), BU(4), BU(5) and BU(6), as described in any of the respective embodiments, respectively, when other than 0, independently ranges from 10 to 100%, or from 10 to 80%, including any subranges and intermediate values therebetween.
By “mol %” it is meant the mol fraction of a backbone unit relative to 1 mol of the polymer, multiplied by 100.
Thus, for example, 50 mol % of BU(3) units describes a polymer composed of 100 backbone units, whereby 50 of its backbone unit are BU(3) and the other 50 backbone units are units of one or more of BU(1), BU(2), BU(4), BU(5) and BU(6).
In other words, 50 mol % of BU(3) units describes a polymer composed of 100 PGA backbone units, in which 50 backbone units are substituted by an —NH-L3-NR3R4 moiety.
In some of any of the embodiments described herein, w, which represents the mol % of BU(1) is 0, such that 100% of the backbone units feature PGA pendant groups that are further substituted, namely, 100% of the backbone units are BU(2), BU(3), BU(4), BU(5) and/or BU(6) backbone units, according to the present embodiments.
In some of any of the embodiments described herein, the polymer comprises a plurality of BU(3) backbone units, such that y in Formula I, which represents the mol % of BU(3), is other than 0. In some of any of the embodiments in which y is other than 0, R3 and R4 are each H.
In some of any of the embodiments in which y is other than 0, L3 is an unsubstituted alkylene being 2 to 10, or 2 to 8, or 2 to 6, carbon atoms in length.
In some of any of the embodiments described herein, y ranges from 50 to 100 mol %, or from 60 to 100 mol %, or from 70 to 100 mol %. In some embodiments, y is about 100 mol %, such that the polymeric compound consists of BU(3) backbone units. In some of these embodiments, R3 and R4 are each hydrogen. In some of these embodiments, L3 is ethylene. See, for example, Polymer A in
In some embodiments, in at least a portion of the plurality of BU(3) backbone units, one or both of R3 and R4 is other than H (hydrogen). In some of these embodiments, R3 and R4 are each methyl. Polymers in which y is other than 0 and R3 and R4 are each other than H comprise backbone units featuring a pendant group that terminates by a tertiary amine. In some of these embodiments, R3 is H and R4 is methyl. Polymers in which y is other than 0 and one of R3 and R4 is other than H comprise backbone units featuring a pendant group that terminates by a secondary amine.
In exemplary embodiments, R3 and R4 are each methyl and L3 is an alkylene, preferably an unsubstituted alkylene being 2 to 6 carbon atoms in length. In some of these embodiments y is about 100 mol %, such that the polymeric compound consists of BU(3) backbone units featuring pedant groups that terminate by a tertiary amine. See, for example, Polymer C in
In some embodiments, in a portion of the BU(3) backbone units R3 and R4 are each hydrogen, according to any of the respective embodiments described herein, and in another portion of the BU(3) backbone units R3 and R4 are each alkyl such as methyl, according to any of the respective embodiments described herein. In some of these embodiments y is about 100 mol %, such that the polymeric compound consists of two types of BU(3) backbone units. See, for example, Polymers D and E in
In some embodiments, in a portion of the BU(3) backbone units R3 and R4 are each hydrogen, according to any of the respective embodiments described herein, and in another portion of the BU(3) backbone one of R3 and R4 is an alkyl such as methyl, according to any of the respective embodiments described herein. In some of these embodiments y is about 100 mol %, such that the polymeric compound consists of two types of BU(3) backbone units. The mol ratio of BU(3) units featuring a primary amine and of BU(3) featuring a secondary amine can be from 1:99 to 99:1, including any intermediate values and subranges therebetween.
In some of any of the embodiments described herein, the polymer comprises a plurality of BU(2) backbone units, such that x in Formula I, which represents the mol % of BU(2), is other than 0.
In some of any of the embodiments described herein, x, which represents the mol % of BU(2), is at least 40 mol %, and at least one of R1 and R2, preferably each, is other than H.
In some of any of the embodiments described herein, x, which represents the mol % of BU(2), ranges from 50 to 100 mol %, or from 60 to 100 mol %, or from 70 to 100 mol %, including any intermediate values and subranges therebetween. In some of any of the embodiments in which x is other than 0, in at least a portion of the plurality of the BU(2) backbone units, one or more of, and preferably each of, R1 and R2 is alkyl, for example, a C1-4 alkyl such as methyl.
In some of any of the embodiments in which x is other than 0, L1 and L2 are each alkylene, and in some embodiments L1 and L2 are each ethylene.
In some of any of the embodiments in which x is other than 0, x is about 100%.
In some of these embodiments, all the BU(2) units are such that R1 and R2 are each an alkyl, as described herein. See, for example, polymer F in
In some of these embodiments, at least 50%, or at least 60% or at least 70% or more of the BU(2) units (at least 50%, or 60% or 70% of y) are units in which each of R1 and R2 is alkyl, for example, methyl, and in the remaining units one or both of R1 and R2 is H. See, for example, Polymer I in
Polymers in which x is other than 0 and R1 and R2 are each hydrogen comprise backbone units featuring a pendant group that comprises a secondary amine and terminates by a primary amine.
Polymers in which x is other than 0 and one of R1 and R2 is other than hydrogen comprise backbone units featuring a pendant group that comprises a secondary amine and terminates by a secondary amine.
Polymers in which x is other than 0 and R1 and R2 are each other than hydrogen comprise backbone units featuring a pendant group that comprises a secondary amine and terminates by a tertiary amine.
In some of any of the embodiments described herein, the polymer comprises a plurality of BU(2) units and a plurality of BU(3) units, as described herein in any of the respective embodiments. In some of these embodiments, x+y is about 100%.
In some of these embodiments, x is at least 40 mol %, and at least one of R1 and R2, preferably each, is other than H. In some of these embodiments, y is lower than 40 mol %, and can also be 0.
In some of any of the embodiments described herein, the polymer comprises a plurality of BU(2) units, wherein in a first portion of the BU(2) units at least one of R1 and R2, preferably each, is other than H, as described herein, and in another portion of the BU(2) units, each of R1 and R2 is H. In some of these embodiments, the first portion of the BU(2) units in which at least one of R1 and R2, preferably each, is other than H is at least 50%, or at least 60%, or at least 70%, of x. In some of these embodiments, x is about 100%. See, for example, Polymer I.
Polymers composed of BU(2) and/or BU(3) backbone units featuring a terminal primary amine, optionally in combination with BU(1) units, are also referred to herein as Group I polymers.
Polymers composed of BU(2) and/or BU(3) backbone units featuring a terminal secondary or tertiary amine, optionally in combination with BU(5) and/or BU(1) units, and further optionally in combination with BU(2) and/or BU(3) backbone units featuring a terminal primary amine, are also referred to herein as Group V polymers.
In some of any of the embodiments described herein, u, which represents the mol % of BU(5) backbone units in the polymer, is other than 0, such that the polymer comprises backbone units featuring alkyl pendant groups. In some of these embodiments, at least one of x, y, z and v is other than 0, such that at least a portion of the backbone units are BU(2), BU(3), BU(4) and/or BU(6).
In some of any of the embodiments described herein, u is at least 40 mol %.
In some of any of the embodiments described herein, u ranges from 40 to 50 mol %, including any intermediate values and subranges therebetween.
In some of any of the embodiments described herein, u is at least 40 mol % and y is other than 0. See, for example, Polymers K, M, O and P, in
In some of these embodiments, y ranges from 60 to 50 mol %, respectively, including any intermediate values and subranges therebetween. That is, for example, u and y together are 100 mol %, and, for example, when u is 40 mol %, y is 60 mol %, when u is 45 mol %, y is 55 mol %, etc.
In some of any of the embodiments described herein, u is at least 40 mol % and x is other than 0. In some of these embodiments, x is at least 40 mol %. See, for example, Polymer X in
In some of any of the embodiments described herein, u is at least 40 mol % and both x and y are other than 0. In some of these embodiments, x is at least 40 mol %. See, for example, Polymer Y in
In some of any of the embodiments described herein for u other than 0, in at least a portion of, or in all of, the plurality of the BU(5) units, R9 is H and R10 is alkyl, as described herein in any of the respective embodiments.
In some of any of the embodiments described herein for u other than 0, in at least a portion of, or in all of, the plurality of the BU(5) units, each of R9 and R10 is alkyl, as described herein in any of the respective embodiments.
The alkyl in these embodiments can be of 3 to 10, or 5 to 10, or 5 to 8, or 6 to 8, carbon atoms in length.
In some of any of embodiments described herein, when u is other than 0, at least one of R9 and R10 is an alkyl being 3 or more, preferably 4 or more, carbon atoms in length, and at least one of x, y, z and v is other than 0.
In some of any of embodiments described herein, when u is other than 0, a first portion of the plurality of the BU(5) units can be such that one of R9 and R10 is hydrogen, as described herein in any of the respective embodiments, and a second portion of the plurality of BU(5) units is such that each of R9 and R10 is other than hydrogen, as described herein in any of the respective embodiments.
Polymers comprising a plurality of BU(5) backbone units in which one of R9 and R10 is hydrogen, in combination with BU(3) units featuring terminal primary amine, and optionally in combination with BU(1) units, are also referred to herein as Group II polymers.
Polymers comprising a plurality of BU(5) backbone units in which each of R9 and R10 is other than hydrogen, in combination with one or more of BU(2) and BU(3), and optionally in combination with BU(1) units, are also referred to herein as Group IV polymers.
In some of any of the embodiments described herein, the polymer comprises a plurality of BU(6) units such that v, which represents the mol % of BU(6) units in the polymer, is other than 0.
In some of these embodiments, v is at least 20, or at least 30 mol %.
In some of any of the embodiments where v is other than 0, and u is at least 20, or at least 30 mol %, such that the polymer comprises, or consists of, a plurality of BU(6) units and a plurality of BU(5) units.
In some of any of the embodiments where v is other than 0, at least one of x, y and z is other than 0, such that the polymer consists of, or comprises, a plurality of BU(6) units in combination with a plurality of BU(2), BU(3) and/or BU(4) units, and optionally further comprises a plurality of BU(5) units.
In some of these embodiments, y is other than 0, such that the polymer consists or comprises a plurality of BU(6) units and a plurality of BU(3) units. In some of these embodiments, u is at least 20, or at least 30 mol %. See, for example, Polymers Q and R, in
In some of any of these embodiments, y ranges from 40 to 80 mol %, preferably from 40 to 60 mol %.
In some of these embodiments, y is other than 0, and u is other than 0, such that the polymer consists or comprises a plurality of BU(6) units, a plurality of BU(3) units and a plurality of BU(5) units. In some of these embodiments, u is at least 20, or at least 30 mol %. In some of any of these embodiments, y ranges from 40 to 60 mol %. In some of these embodiments, u ranges from 20 to 40 mol %. See, for example, Polymers S and T, in
In some of any of the embodiments described herein, Z is a nitrogen-containing heteroaryl, for example, imidazole.
Polymers composed of BU(6), optionally in combination with BU(2), BU(3), BU(4) and/or BU(5), and further optionally in combination with BU(1) units, are also referred to herein as Group III polymers.
In some of any of the embodiments described herein, the polymer comprises a plurality of BU(4) backbone units, as described herein in any of the respective embodiments, optionally in combination with a plurality of backbone units of one or more of BU(2), BU(3), BU(5) and/or BU(6), and further optionally in combination with BU(1). In some of these embodiments, z, which represents the mol % of BU(4) units, at least 20%, or at least 30%, or at least 40%.
In some embodiments, the polymers described and exemplified herein in embodiments of Formula I are constructed of a PGA backbone and pending functional moieties (pendant groups) attached to the backbone via the carboxylic groups, preferably via an amide bond. The pendant groups can comprise primary, secondary and/or tertiary amines (as in BU(2) and BU(3) units), heterocyclic moieties (as in BU(6) units), linear and/or branched alkyls (as in BU(5) units), and/or branched alkyls terminating by primary., secondary and/or tertiary amines (as in BU(4) units).
In exemplary embodiments, a polymeric compound represented by Formula I as described herein is represented by Formula Ia as follows:
wherein, in some embodiments:
Y is (CH2)a, and a is an integer of from 2 to 6;
R1 is H;
R2 is (CH2)bCH3, and b is an integer of from 4 to 8,
and, in some embodiments,
Y is (CH2)a, and a is an integer of from 2 to 6;
R1 and R2 are each independently (CH2)bCH3, wherein b is an integer of from 2 to 5,
and wherein for each of these embodiments, n, m, p and q represent the mol % of exemplary BU(3) units (n), exemplary BU(5) units (m), exemplary BU(6) units (p) and exemplary BU(1) units (q), whereas n ranges from 40 to 100%, m ranges from 0 to 45%, p ranges from 0 to 30%, and q ranges from 0 to 60%.
In some embodiments, n, m, p and q correspond to y, u, v and q in Formula I, respectively, as described herein in any of the respective embodiments.
In some of any of these embodiments, k is 4-18, and (CH2)k is an exemplary Ra group, as defined herein for Formula I.
In some of any of these embodiments, Rb is as described herein for Formula I.
In some embodiments, polymers represented by Formula Ia comprise, as a pendant group of some backbone units, a linear alkyl amine moiety bearing 2-6 carbon atoms, wherein a mol % (n) of backbone units bearing such a pendant group is 40-100 mol %; and may further comprise as a pendant group of another portion of the backbone units a linear alkyl moiety of 6-10 carbons or branched alkyl moieties of 8-14 carbons, wherein a mol % (m) of backbone units bearing such a pendant group is 0-45%; and/or a pendant group comprising an imidazole ring conjugated via ethylene or another alkylene to the carboxylic acid of another portion of backbone units, wherein a mol % (p) of backbone units bearing such a pendant group is 0-30%; and wherein the remaining backbone units feature a carboxylic acid-containing pendant group of PGA, wherein a mol % (q) of backbone units bearing such a pendant group is 0-60%.
In exemplary embodiments, a polymeric compound represented by Formula I as described herein is represented by Formula Ib as follows:
wherein:
Y is (CH2)a, and a is an integer of from 2 to 10;
X═(CH2)a′, and a′ is an integer of from 2 to 10;
W is H or CH3;
R1 is (CH2)bCH3, and b is an integer of from 4 to 8;
R2 is H or is (CH2)bCH3, and b is an integer of from 4 to 8;
C is an integer of from 2 to 6; and
A is N or CH2,
and wherein for each of these embodiments, n, m, p, 1 and q represent the mol % of exemplary BU(2) and/or BU(3) units (n), exemplary BU(5) units (m), exemplary BU(6) units (p), exemplary BU(3) units (1), and exemplary BU(1) units (q), whereas n ranges from 40 to 100%, m ranges from 0 to 45%, p ranges from 0 to 30%, 1 ranges from 0 to 30%, and q ranges from 0 to 60%.
In some embodiments, n, m, p, 1 and q correspond to x, u, v, y and q, respectively, in Formula I, as described herein in any of the respective embodiments.
In some of any of these embodiments, k is 4-18, and (CH2)k is an exemplary Ra group, as defined herein for Formula I.
In some embodiments, polymers represented by Formula Ib comprise, comprise, as a pendant group of some backbone units thereof, a linear alkyl chain bearing 4-20 carbon atoms terminated by a secondary or tertiary amine, and optionally featuring an additional secondary amine at the middle of the alkyl chain, wherein a mol % (n) of backbone units bearing such a pendant group is 40-100%; and may further comprise, as a pendant group of another portion of the backbone units, a linear alkyl moiety of 6-10 carbons or branched alkyl moiety of 4-7 carbons in case of short (4-6 carbons) alkyl chain in the first moiety, wherein a mol % (m) of backbone units bearing such a pendant group is 0-45%; and/or a pendant group comprising an imidazole ring conjugated via ethylene or other alkylene to the carboxylic acid groups of another portion of backbone units, wherein a mol % (p) of backbone units bearing such a pendant group is 0-30%; and/or as a pendant group of another portion of the backbone units, a linear alkyl amine moiety of 2-6 carbons, wherein a mol % (1) of backbone units bearing such a pendant group is 0-50%; and wherein the remaining backbone units feature a carboxylic acid-containing pendant group of PGA, wherein a mol % (q) of backbone units bearing such a pendant group is 0-60%.
In exemplary embodiments, a polymeric compound represented by Formula I as described herein is represented by Formula Ic as follows:
wherein, in some embodiments:
X is independently H or CH3;
R1 is (CH2)bCH3, and b is an integer ranging from 4 to 8; and
R2 is H,
and in some embodiments:
X is H or CH3;
R1 and R2 are each independently (CH2)bCH3, and b is an integer of from 2 to 5,
and, in some embodiments:
X is H or CH3;
R1 is (CH2)2NH(CH2)5CH3; and
R2 is H,
and, wherein, for each of these embodiments, n, m, p and q represent the mol % of exemplary BU(4) units (n), exemplary BU(5) units (m), exemplary BU(6) units (p), and exemplary BU(1) units (q), whereas n ranges from 40 to 100%, m ranges from 0 to 45%, p ranges from 0 to 30%, and q ranges from 0 to 60%.
In some embodiments, n, m, p and q correspond to z, u, v, and q, respectively, in Formula I, as described herein in any of the respective embodiments.
In some embodiments, polymers represented by Formula Ic comprise, as a pendant group of some backbone units thereof, a branched alkyl amine bearing either primary, secondary or tertiary terminal amines, wherein a mol % (n) of backbone units bearing such a pendant group is 40-100% rate; and may optionally further comprises, as a pendant group of another portion of the backbone units, a linear or branched alkyl chain bearing 6-14 carbon atoms with or without a secondary amine at the middle of the alkyl chain, wherein a mol % (m) of backbone units bearing such a pendant group is 0-45%; and/or as a pendant group, an imidazole ring conjugated via ethylene or another alkylene to the carboxylic acid of another portion of the backbone units, wherein a mol % (p) of backbone units bearing such a pendant group is 0-30%; and wherein the remaining backbone units feature a carboxylic acid-containing pendant group of PGA, wherein a mol % (q) of backbone units bearing such a pendant group is 0-60%.
In some embodiments, the polymers represented by Formula Ia, Ib or Ic have an N-terminus unit of linear alkyl bearing 4-18 carbons.
In some of any of the embodiments described herein for Formulae I, Ia, Ib and Ic, the polymer comprises BU(3) backbone units, at a mol % (x or a variable corresponding thereto) of at least 40%, and at least one, and preferably both, of R1 and R2 is other than H. In some of these embodiments, if the polymer further comprises BU(2) backbone units, the mol % of BU(2) units (y or a variable corresponding thereto) is lower than 40%.
In some of any of the embodiments described herein for Formulae I, Ia, Ib and Ic, the polymer comprises BU(5) backbone units, and at least one of R9 and R10 is an alkyl being more than 3 carbon atoms in length, as described herein in any of the respective embodiments. In any of these embodiments, at least one of x, y, z and v, or variables corresponding thereto, is other than 0.
In some of any of the embodiments described herein for Formulae I, Ia, Ib and Ic, when the polymer comprises BU(6) backbone units, it comprises also a plurality of BU(5) units, such that v and u, or any of the variables corresponding thereto, is other than 0, as described herein in any of the respective embodiments.
In some of any of the embodiments described herein for Formulae I, Ia, Ib and Ic, the polymer comprises BU(4) backbone units, at a mol % (z or a variable corresponding thereto) of at least 40%.
In some of any of the embodiments described herein, the polymers described herein are collectively represented by Formula I*:
wherein:
x, y, z, u, v and w each independently represents the mol % of the respective backbone unit, such that x+y+z+u+v+w=100 mol %, wherein x+y+z+u+v≥40 mol %;
Ra is selected from hydrogen (in case an N-terminus group is amine) and alkyl, preferably an alkyl (linear or branched) of at least 4 carbon atoms in length, representing an alkyl substituent of an N-terminus amine, as described herein), as described herein for any of the respective embodiments of Formula I, Ia, Ib and/or Ic;
Rb is selected from hydroxyl (in case a C-terminus group is carboxylic acid), alkoxy (in case a C-terminus group is a carboxylate), amine (in case a C-terminus group is an amide) and pyrrolidinone (in case a C-terminus group is amide formed with a nitrogen-containing heterocyclic group), as described herein for any of the respective embodiments of Formula I, Ia, Ib and/or Ic;
R1-R11 are each independently selected from H, alkyl and cycloalkyl, as defined herein and as described in any one of the respective embodiments and any combination thereof for any of Formula I, Ia, Ib and/or Ic;
L1, L2, L3 and L6 is each independently a linear (non-branched) linking moiety, as defined herein and as described in any one of the respective embodiments and any combination thereof for Formula I;
L4 is a branched linking moiety, as defined herein and as described in any one of the respective embodiments and any combination thereof, for BU(4), and for Formula I;
L5 is a linear linking moiety or a branched linking moiety, or is absent, as defined herein and as described in any one of the respective embodiments and any combination thereof, for BU(5), and for Formula I; and
Z is a nitrogen-containing heterocylic moiety, as described in any one of the respective embodiments and any combination thereof, for BU(6), and for Formula I,
provided that:
(i) x is at least 40 mol %, y is lower than 40 mol %, and at least one of R1 and R2 is other than H; or
(ii) when u is other than 0, at least one of R9 and R10 is an alkyl being more than 3 carbon atoms in length, and at least one of x, y, z and v is other than 0; or
(iii) when v is other than 0, u is other 0; or
(iv) z is greater than 40 mol %.
Exemplary polymers according to some embodiments of the present invention include Polymers A-Y, as shown in the Examples section and in
Exemplary polymers according to some embodiments of the present invention include Polymer A, Polymer B, Polymer F, Polymer I, Polymer K, Polymer M, Polymer O, Polymer P, and Polymer T.
In some embodiments, Exemplary polymers according to some embodiments of the present invention include Polymer F, Polymer I, Polymer K, Polymer M, Polymer O, Polymer P, and Polymer T, as described herein.
According to an aspect of some embodiments of the present invention there are provided processes of preparing the polymers of Formula I as described herein. The processes are generally effected by coupling PGA to a respective amine-containing moiety, as described herein.
Any coupling agent useful in forming peptide bonds is contemplated. One or more types of coupling agents can be used, depending on the type(s) of the amine to be conjugated.
Exemplary coupling agents include, without limitation, CDI and DIC.
Cross-Linked Polymers:
In some embodiments of the present invention, there is provided a polymer as described herein in any of the respective embodiments, which further comprises BU(8) units as described herein, in any of the respective embodiments. Such polymers are cross-linked polymers (co-polymers), and can be collectively represented by Formula II, as described herein:
wherein:
Q1 and Q4 are each independently selected from an N-terminus group, as defined herein and a polymeric chain comprising a plurality of one or more of BU(1), BU(2), BU(3), BU(4), BU(5), BU(6) and BU(7) backbone units; and
Q2 and Q3 are each independently selected from an C-terminus group, as defined herein and a polymeric chain comprising a plurality of one or more of BU(1), BU(2), BU(3), BU(4), BU(5), BU(6) and BU(7) backbone units,
provided that at least one of Q1, Q2, Q3 and Q4 comprises a plurality of one or more of BU(2), BU(3), BU(4), and BU(6) backbone units.
In some embodiments, one or more of Q1, Q2, Q3 and Q4 is a polymeric chain that corresponds to any one of the polymers of Formula I, Ia, Ib, Ic or I*, as described herein in any of the respective embodiments, such that a polymer represented by one of these Formulae is a cross-linked polymer.
In some of any of the embodiments described herein for Formula II, the mol % of the BU(8) in the cross-linked polymer ranges from 1 to 20%, and the mol % of the other backbone units (e.g., of BU(1), BU(2), BU(3), BU(4), BU(5), BU(6) and/or BU(7)) ranges from 99 to 80%, respectively.
In some of any of the embodiments described herein for Formula II, BU(8) represents cross-linked lysine moieties, such that L8 is formed upon cross-linking the terminal amine group of one lysine with a terminal amine group of another lysine. Alternatively, BU(8) can be a cross-linked form of any other amino acid featuring an amine-containing pendant groups. When amine-containing pendant groups are cross-linked by, for example, a dialdehyde such as glutaraldehyde, L8 represents a cross-linking moiety that comprises two Schiff base moieties linking alkylene chains. Alternatively, BU(8) can be any of the other cross-linked amide acids as described herein.
An exemplary polymer of Formula II, referred to herein as Polymer PL1, is depicted in
In Polymer CL1, the cross-linked polylysine is attached to polymeric backbones comprising or consisting of BU(3) units featuring a terminal primary amine.
Co-Polymers:
In some embodiments of the present invention, there is provided a polymer as described herein in any of the respective embodiments, which further comprises BU(7) units as described herein, in any of the respective embodiments.
In some of these embodiments, the polymer comprises a plurality of backbone units selected from BU(1), BU(2), BU(3), BU(4), BU(5), and/or BU(6), and a plurality of BU(7) backbone units, as described herein in any of the respective embodiments.
In some embodiments, at least 40 mol % of the backbone units are selected from BU(2), BU(3), BU(4), and/or BU(6).
In some embodiments, the polymer is arranged as a block-copolymer comprising at least one block comprising a plurality of BU(1), BU(2), BU(3), BU(4), BU(5), and/or BU(6), and at least one block comprising BU(7) backbone units.
In some embodiments, a total mol % of the BU(2), BU(3), BU(4), BU(5), and/or BU(6) is at least 60%.
Such polymers can alternatively be collectively represented by Formula III, as described herein:
[Qa]m-[M]p Formula III
wherein:
M comprises one or more BU(7) backbone units as defined herein in any of the respective embodiments;
Qa comprises one or more (e.g., a plurality) of backbone units selected from BU(1), BU(2), BU(3), BU(4), BU(5), and/or BU(6), and optionally BU(8), as described herein for any of the embodiments Formula I, Ia, Ib, Ic and II, and any combination thereof,
p, which represents the total mol % of BU(7) units ranges from 20 to 40; and
m, which represents the total mol % of BU(1), BU(2), BU(3), BU(4), BU(5), and/or BU(6), and optionally BU(8, ranges from 60 to 80, respectively,
provided that Qa comprises a plurality of one or more of BU(2), BU(3), BU(4), and BU(6) backbone units.
In some embodiments, Qa and m are such that the total mol % of the BU(2), BU(3), BU(4), and BU(6) backbone units, whichever present, is at least 40%.
In some embodiments, Qa and m are as described herein for polymers of Formula I, Ia, Ib or Ic, in any of the respective embodiments and any combination thereof.
The BU(7) units and the backbone units of Qa can be arranged in the polymeric backbone in any order, as is known in the art for co-polymers.
In some embodiments, the BU(7) backbone units can be interlaced randomly within the backbone units composing Qa.
In some embodiments, the BU(7) and backbone units of Qa are arranged as a block co-polymer, comprising one or more clusters of the backbone units composing Qa and one or clusters of BU(7) backbone units.
For example, the block co-polymer can be arranged as follows:
[M′]g-[Qa′]h-[M′]f-[Q′a′]i
wherein:
M′ is a block comprising a plurality of BU(7) backbone units;
Qa′ is a block comprising a plurality of backbone units as described herein for Formula I, Ia, Ib, or Ic;
g and f represent the mol % of each M′ block,
h and i represent the mol % of each Qa′ block,
g ranges from 0 to 40;
f ranges from 0 to 40;
h ranges from 40 to 80; and
i ranges from 0 to 40,
such that g+f ranges from 20 to 40 and h+i ranges from 60 to 80, and g+h+f+1=100.
Thus, for example, g can be 20-40, h can be 80-60, respectively, and f and i are each 0. Alternatively, g is 10-20, h is 60-80, and f is 10-20. Further alternatively, g is 0, h is 30-40, f is 20-40, and i is 30-40. Any other values are contemplated.
The block copolymer can include more than 2 Qa′ blocks and/or more than 2 M′ blocks.
When two or more blocks of Qa′ are present, the blocks of Qa′ can include the same or different composition of backbone units, and in some embodiments, each of the Qa′ blocks is the same.
In some embodiments, each Qa′ block comprises one type of backbone units (for example, one type of BU(2), BU(3), BU(4) or BU(6), or two or more types, as described herein for any of the embodiments of Formula I.
In some embodiments, each of the Qa′ blocks consists of BU(3) backbone units, and in some of these embodiments, the BU(3) backbone units feature a primary terminal amine.
When two or more M′ blocks are present, the M′ blocks can include the same or different composition of BU(7) backbone units, and in some embodiments, each of the M′ blocks is the same.
In some embodiments, a M′ block comprises one type of BU(7) backbone units, or two or more types.
The BU(7) units can be, for example, any of the naturally occurring amino acid bearing an alkyl pendant group (e.g., alanine, valine, leucine, isoleucine), or can be a synthetic amino acid.
In some embodiments, a copolymer of Formula III comprises a block co-polymer of α-alkyl-amino acid (20-40%) and L-polyglutamate (80-60%) backbone in which the glutamate units include one or more of BU(1), BU(2), BU(3), BU(4), BU(5), and/or BU(6), and optionally BU(8), as described herein for any of the embodiments Formula I, Ia, Ib, Ic and II, and any combination thereof.
In some embodiments, block copolymers of Formula III can be represented by Formula IIIa:
wherein A, B, A′ and B′ represent the mol % of the respective backbone units in each block.
Polymers of Formula III are also referred to herein as Polymers of Group V.
Polymers of Formula III can be prepared by co-polymerizing a plurality of glutamate units and a plurality of BU(7) (or precursors thereof) under conditions that form a respective block-copolymer, and thereafter modifying some or all of the glutamate units to provide the respective BU(2), BU(3), BU(4), BU(5), and/or BU(6) backbone units, as described herein for polymers of Formula I.
If the Qa or Qa′ comprises BU(8) units, such units are co-polymerized with the glutamate and BU(7) units.
The Conjugate:
A conjugate as described herein comprises a polymer as described herein in any one of the respective embodiments and any combination thereof, including any of the block co-polymers and cross-linked polymers and any of the respective embodiments thereof, in association with an oligonucleotide, as described herein.
By “association”, “associated with” and any grammatical diversion of these terms, it is meant that that the oligonucleotide and the polymer are linked to one another via one or more chemical and/or physical interactions.
In some embodiments, the oligonucleotide is complexed to the polymer, and the conjugate is therefore referred to herein interchangeably as a polyplex.
In some embodiments, the association is by electrostatic interactions, or bonds, formed between the amine moieties and optionally other nitrogen-containing moieties (e.g., imidazole) in the polymer and the negatively charged groups of the oligonucleotide.
In some embodiments, the electrostatic interactions are between terminal amine groups or other terminal nitrogen-containing moieties (e.g., imidazole) of the polymer and phosphate groups of the oligonucleotide.
N/P ratio is the ratio between phosphate groups of the oligonucleotide and terminal amines of the pendant groups of the PGA backbone. For example: 5 N/P means 5 terminal nitrogen groups for each phosphate group (can be also written as 5:1 ratio).
In some embodiments, this N/P ratio between a number of the terminal amine groups and a number of the phosphate groups ranges from 15:1 to 1:1, or from 10:1 to 1:1, or from 5:1 to 1:1.
The term “oligonucleotide” refers to a single stranded or double stranded oligomer or polymer of ribonucleic acid (RNA) or deoxyribonucleic acid (DNA) or mimetics thereof. This term includes oligonucleotides composed of naturally-occurring bases, sugars and covalent internucleoside linkages (e.g., backbone) as well as oligonucleotides having non-naturally-occurring portions which function similarly to respective naturally-occurring portions.
In some embodiments, the oligonucleotide is an RNA nucleotide. In some embodiments, the oligonucleotide is an RNA silencing agent.
As used herein, the phrase “RNA silencing” refers to a group of regulatory mechanisms [e.g. RNA interference (RNAi), transcriptional gene silencing (TGS), post-transcriptional gene silencing (PTGS), quelling, co-suppression, and translational repression] mediated by RNA molecules which result in the inhibition or “silencing” of the expression of a corresponding protein-coding gene.
As used herein, the term “RNA silencing agent” refers to an RNA which is capable of specifically inhibiting or “silencing” the expression of a target gene. In certain embodiments, the RNA silencing agent is capable of silencing mRNA in a cell. In some embodiments, the RNA silencing agent is capable of preventing complete processing (e.g., the full translation and/or expression) of an mRNA molecule through a post-transcriptional silencing mechanism. RNA silencing agents include noncoding RNA molecules, for example RNA duplexes comprising paired strands, as well as precursor RNAs from which such small non-coding RNAs can be generated. Exemplary RNA silencing agents include dsRNAs such as siRNAs, miRNAs and shRNAs. In one embodiment, the RNA silencing agent is capable of inducing RNA interference. In another embodiment, the RNA silencing agent is capable of mediating translational repression.
RNA interference refers to the process of sequence-specific post-transcriptional gene silencing in animals mediated by short interfering RNAs (siRNAs). The process of post-transcriptional gene silencing is thought to be an evolutionarily-conserved cellular defense mechanism used to prevent the expression of foreign genes and is commonly shared by diverse flora and phyla. Such protection from foreign gene expression may have evolved in response to the production of double-stranded RNAs (dsRNAs) derived from viral infection or from the random integration of transposon elements into a host genome via a cellular response that specifically destroys homologous single-stranded RNA or viral genomic RNA.
The term “siRNA” refers to small inhibitory RNA duplexes (generally between 18-30 basepairs) that induce the RNA interference (RNAi) pathway.
Typically, siRNAs are chemically synthesized as 21mers with a central 19 bp duplex region and symmetric 2-base 3′-overhangs on the termini, although it has been recently described that chemically synthesized RNA duplexes of 25-30 base length can have as much as a 100-fold increase in potency compared with 21mers at the same location. The observed increased potency obtained using longer RNAs in triggering RNAi is theorized to result from providing Dicer with a substrate (27mer) instead of a product (21mer) and that this improves the rate or efficiency of entry of the siRNA duplex into RISC.
It has been found that position of the 3′-overhang influences potency of an siRNA and asymmetric duplexes having a 3′-overhang on the antisense strand are generally more potent than those with the 3′-overhang on the sense strand (Rose et al., 2005). This can be attributed to asymmetrical strand loading into RISC, as the opposite efficacy patterns are observed when targeting the antisense transcript.
The strands of a double-stranded interfering RNA (e.g., an siRNA) may be connected to form a hairpin or stem-loop structure (e.g., an shRNA). Thus, as mentioned, the RNA silencing agent of some embodiments of the invention may also be a short hairpin RNA (shRNA).
The term “shRNA”, as used herein, refers to an RNA agent having a stem-loop structure, comprising a first and second region of complementary sequence, the degree of complementarity and orientation of the regions being sufficient such that base pairing occurs between the regions, the first and second regions being joined by a loop region, the loop resulting from a lack of base pairing between nucleotides (or nucleotide analogs) within the loop region. The number of nucleotides in the loop is a number between and including 3 to 23, or 5 to 15, or 7 to 13, or 4 to 9, or 9 to 11. Some of the nucleotides in the loop can be involved in base-pair interactions with other nucleotides in the loop.
Examples of oligonucleotide sequences that can be used to form the loop include 5′-UUCAAGAGA-3′ (Brummelkamp, T. R. et al. (2002) Science 296: 550) and 5′-UUUGUGUAG-3′ (Castanotto, D. et al. (2002) RNA 8:1454). It will be recognized by one of skill in the art that the resulting single chain oligonucleotide forms a stem-loop or hairpin structure comprising a double-stranded region capable of interacting with the RNAi machinery.
According to some embodiments, the RNA silencing agent may be a miRNA.
The term “microRNA”, “miRNA”, and “miR” are synonymous and refer to a collection of non-coding single-stranded RNA molecules of about 19-28 nucleotides in length, which regulate gene expression. miRNAs are found in a wide range of organisms (viruses.fwdarw.humans) and have been shown to play a role in development, homeostasis, and disease etiology.
The term “microRNA mimic” refers to synthetic non-coding RNAs that are capable of entering the RNAi pathway and regulating gene expression. miRNA mimics imitate the function of endogenous microRNAs (miRNAs) and can be designed as mature, double stranded molecules or mimic precursors (e.g., or pre-miRNAs). miRNA mimics can be comprised of modified or unmodified RNA, DNA, RNA-DNA hybrids, or alternative nucleic acid chemistries (e.g., LNAs or 2′-O,4′-C-ethylene-bridged nucleic acids (ENA)). For mature, double stranded miRNA mimics, the length of the duplex region can vary between 13-33, 18-24 or 21-23 nucleotides. The miRNA may also comprise a total of at least 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 or 40 nucleotides. The sequence of the miRNA may be the first 13-33 nucleotides of the pre-miRNA. The sequence of the miRNA may also be the last 13-33 nucleotides of the pre-miRNA.
It will be appreciated that the RNA silencing agent of some embodiments of the invention need not be limited to those molecules containing only RNA, but further encompasses chemically-modified nucleotides and non-nucleotides.
A conjugate as described herein can comprise one or more types of an oligonucleotide in association therewith. In some embodiments, the conjugate comprises two oligonucleotides that act in synergy. Exemplary such oligonucleotides are as described in Example 8 hereinbelow. In some of these embodiments, the conjugate comprises a siRNA and a mi-RNA, for example, as exemplified in Example 8 hereinbelow.
mRNAs to be targeted using RNA silencing agents include, but are not limited to, those whose expression is correlated with an undesired phenotypic trait. Exemplary mRNAs that may be targeted are those that encode truncated proteins i.e. comprise deletions. Accordingly the RNA silencing agent of some embodiments of the invention may be targeted to a bridging region on either side of the deletion. Introduction of such RNA silencing agents into a cell would cause a down-regulation of the mutated protein while leaving the non-mutated protein unaffected.
A conjugate as described herein can further comprise other moieties associated therewith, such as, but not limited to, a labeling agent, as described herein, a targeting moiety, an additional therapeutically active agent, and any other moiety, as desired. In some embodiments, the additional moiety is attached to the conjugate via chemical bonds (e.g., covalent bonds), for example, to one or more of the backbone units, or to one or more of the termini of the polymeric backbone.
In some embodiments, the additional moiety is a cell-penetrating peptide. Exemplary peptides include those described in Milletti Drug Discov Today. 2012; 17:850-60, TAT peptides as described, for example, in Frankel et al. Cell. 1988; 55:1189-93, TAT-like structures as described, for example, in Bersani et al. Bioconjugate chemistry. 2012; 23:1415-25, and mitochondria-disrupting peptides, as described, for example, in Javadpour et al. Journal of medicinal chemistry. 1996; 39:3107-13. Such cell-penetrating peptides may promote cellular uptake of the conjugates. Any other moiety that promotes cellular uptake is also contemplated.
As used herein, a “cell-penetrating peptide” is a peptide that comprises a short (about 12-30 residues) amino acid sequence or functional motif that confers the energy-independent (i.e., non-endocytotic) translocation properties associated with transport of the membrane-permeable complex across the plasma and/or nuclear membranes of a cell. The cell-penetrating peptide used in the membrane-permeable complex of some embodiments of the invention preferably comprises at least one non-functional cysteine residue, which is either free or derivatized to form a disulfide link with a double-stranded ribonucleic acid that has been modified for such linkage. Representative amino acid motifs conferring such properties are listed in U.S. Pat. No. 6,348,185, the contents of which are expressly incorporated herein by reference. The cell-penetrating peptides of some embodiments of the invention preferably include, but are not limited to, penetratin, transportan, pIsl, TAT(48-60), pVEC, MTS, and MAP.
Targeting moieties or agents suitable for use in the context of the present embodiments include ligands of cell-surface receptors expressed in tumor cells.
Exemplary moieties or agents include, without limitation, an arginine-glycine-aspartate (RGD) peptide, fibronectin, folate, galactose, an apolipoprotein, insulin, transferrin, a fibroblast growth factor (FGF), an epidermal growth factor (EGF), and an antibody. In an embodiment, the targeting agent can interact with a receptor selected from αv,β3-integrin, folate, asialoglycoprotein, a low-density lipoprotein (LDL), an insulin receptor, a transferrin receptor, a fibroblast growth factor (FGF) receptor, an epidermal growth factor (EGF) receptor, and an antibody receptor. In some embodiments, the arginine-glycine-aspartate (RGD) peptide can be cyclic (fKRGD). NCAM targeting moieties are also contemplated. Bisphosphonates such as alendronate are also contemplated.
As used herein, the phrase “labeling agent” describes a detectable moiety or a probe. Exemplary labeling agents which are suitable for use in the context of the these embodiments include, but are not limited to, a fluorescent agent, a radioactive agent, a magnetic agent, a chromophore, a bioluminescent agent, a chemiluminescent agent, a phosphorescent agent and a heavy metal cluster.
The phrase “radioactive agent” describes a substance (i.e. radionuclide or radioisotope) which loses energy (decays) by emitting ionizing particles and radiation. When the substance decays, its presence can be determined by detecting the radiation emitted by it. For these purposes, a particularly useful type of radioactive decay is positron emission. Exemplary radioactive agents include 99mTc, 18F, 131I and 125I.,
The term “magnetic agent” describes a substance which is attracted to an externally applied magnetic field. These substances are commonly used as contrast media in order to improve the visibility of internal body structures in Magnetic Resonance Imaging (MRI). The most commonly used compounds for contrast enhancement are gadolinium-based. MRI contrast agents alter the relaxation times of tissues and body cavities where they are present, which, depending on the image weighting, can give a higher or lower signal.
As used herein, the term “chromophore” describes a chemical moiety that, when attached to another molecule, renders the latter colored and thus visible when various spectrophotometric measurements are applied.
The term “bioluminescent agent” describes a substance which emits light by a biochemical process
The term “chemiluminescent agent” describes a substance which emits light as the result of a chemical reaction.
The phrase “fluorescent agent” refers to a compound that emits light at a specific wavelength during exposure to radiation from an external source. Exemplary such labeling agents include agents that emit light at the Near IR range (e.g., cyanines).
The phrase “phosphorescent agent” refers to a compound emitting light without appreciable heat or external excitation as by slow oxidation of phosphorous.
A heavy metal cluster can be for example a cluster of gold atoms used, for example, for labeling in electron microscopy techniques.
Uses:
The conjugates described herein can be used for delivering the oligonucleotide into a cell, thus for transfecting a cell.
By “cell” are encompassed prokaryotic or eukaryotic cells, preferably animal cells, mammalian cells, and human cells.
The conjugates described herein are designed to release the oligonucleotide in the cell.
The conjugate is such that the oligonucleotide is releasably associated with the polymer.
In some embodiments, the conjugates as described herein are for use in gene therapy, particularly, gene silencing.
In some embodiments, the conjugates described herein are for use in silencing a gene in a cell.
In some embodiments, the conjugates described herein are for use in the treatment of medical conditions treatable by gene silencing, as described herein.
In some embodiments, the conjugates described herein are for use in the treatment of medical conditions characterized by impaired siRNA and/or miRNA genetic regulation.
Exemplary medical conditions treatable by the conjugates as described herein include, but are not limited to cancer (e.g., solid tumors), viral infections and diseases, cardiovascular diseases, metabolic diseases, neurodegenerative diseases, autoimmune diseases such as rheumatoid arthritis, and genetic diseases and disorders.
Exemplary genes to be targeted by the silencing therapy described herein include, but are not limited to, cancer-related such as K-ras, Rac1, Plk1, c-myc, bcr/abl, c-myb, c-fms, c-fos and cerb-B, growth factor genes (e.g., genes encoding epidermal growth factor and its receptor, fibroblast growth factor-binding protein), matrix metalloproteinase genes (e.g., the gene encoding MMP-9), adhesion-molecule genes (e.g., the gene encoding VLA-6 integrin), tumor suppressor genes (e.g., bcl-2 and bcl-X1), angiogenesis genes, and metastatic genes; rheumatoid arthritis-related genes include, for example, genes encoding stromelysin and tumor necrosis factor; viral genes include human papilloma virus genes (related, for example, to cervical cancer), hepatitis B and C genes, and cytomegalovirus (CMV) genes (related, for example, to retinitis). Numerous other genes relating to these diseases or others are also contemplated.
According to an aspect of some embodiments of the present invention there is provided a use of the conjugates described herein in the manufacture of a medicament for delivering the oligonucleotide to a cell, and/or for silencing a gene in a cell, and/or for use in gene therapy or gene silencing, as described herein. The medicament can be a pharmaceutical composition as described herein.
According to an aspect of some embodiments of the present invention there is provided a method of delivering an oligonucleotide to a cell, and/or for silencing a gene in a cell, and/or for treating a medical condition treatable by gene therapy or gene silencing as described herein, which is effected by contacting the cell with a conjugate as described herein in any of the respective embodiments.
The contacting can be effected in vivo, ex-vivo or in vivo. When the contacting is in vivo, the method comprises administering to a subject in need thereof (e.g., in which silencing a gene is beneficial) a conjugate as described herein in any of the respective embodiments.
The contacting can be effected by any method known in the art.
In some of any of the embodiments described herein for the methods and uses of the conjugates, two or more conjugates are utilized, each conjugate comprises a different oligonucleotide is association with the polymer.
In some of these embodiments, one conjugate comprises a siRNA and one conjugate comprises a mi-RNA, for example, miRNA as exemplified in the Examples section that follows. In some embodiments, the two or more oligonucleotides associated with the two or more polymers act in synergy.
Pharmaceutical Compositions:
According to some of any of the embodiments described herein there is provided a pharmaceutical composition comprising a conjugate as described herein in any of the respective embodiments, and a pharmaceutically acceptable carrier.
In some embodiments, the pharmaceutical composition is for use in any of the methods and uses described herein.
According to some embodiments of the present invention a pharmaceutical composition comprising the conjugate as described herein comprises an aqueous carrier.
A pharmaceutical composition as described herein is also referred to as a formulation.
According to some embodiments, the conjugate is in a form of a plurality of particles (e.g., nanoparticles) dispersed in the carrier.
According to some embodiments, the carrier further comprises a dispersing agent.
According to some embodiments, the carrier further comprises glucose.
According to some embodiments, the dispersing agent is selected so as to prevent aggregation of the nanoparticles and/or to maintain the discrete particles of the conjugate in the composition.
According to some embodiments, the dispersing agent is selected so as to obtain and maintain nanoparticles featuring an average particle size (diameter) of said particles is lower than 1 micron, or lower than 500 nm or lower than 300 nm, or lower than 200 nm and/or PDI lower than 1, or lower than 0.5, or lower than 0.3.
In some embodiments, for conjugates in which the polymer features amine-containing groups (e.g., primary amine-containing groups, such as PGAamine A), the dispersing agent is a surfactant, such as Tween®. Other surfactants are also contemplated.
In some embodiments, a concentration of the surfactant ranges from 0.1% to 40% by volume, of the total volume of the composition.
In some embodiments, a concentration of the surfactant ranges from 0.1 to 10, or from 0.1 to 40 mol %, relative to the conjugate.
In some embodiments, for conjugates in which the polymer features amine-containing pendant groups and alkyl-containing pendant groups, the dispersing agent can be a polyethylene glycol and/or a glucose (for isotonicity) as described herein.
In some embodiments, a concentration of the PEG ranges from 1 to 20%, or from 5 to 15%, or is about 10%, by volume, of the total volume of the composition.
In some embodiments, a MW of the PEG is at least 400 grams/mol.
In some embodiments, a concentration of the glucose ranges from 1 to 20%, or from 1 to 15%, or from 1 to 10%, by volume, of the total volume of the composition.
In some embodiments, for conjugates in which the polymer features amine-containing pendant groups and alkyl-containing pendant groups, the composition is prepared by means of a microfluidic system.
According to an aspect of some embodiments of the present invention there is provided a pharmaceutical composition comprising a pharmaceutically acceptable carrier, e.g., an aqueous carrier, and a conjugate which comprises a polymer represented by Formula I, as described herein in any of the respective embodiments, and an oligonucleotide associated with said polymer, wherein the conjugate is in a form of particles dispersed in said carrier, and wherein an average particle size (in diameter) of said particles is lower than 1 micron, or lower than 500 nm or lower than 300 nm, or lower than 200 nm; and/or a PDI of said particles is lower than 1, or lower than 0.5, or lower than 0.3.
As used herein a “pharmaceutical composition” refers to a preparation of one or more of the active ingredients described herein with other chemical components such as physiologically suitable carriers and excipients. The purpose of a pharmaceutical composition is to facilitate administration of a compound to an organism.
Herein the term “active ingredient” refers to the conjugate (polyplex) accountable for the biological effect, as described herein.
Hereinafter, the phrases “physiologically acceptable carrier” and “pharmaceutically acceptable carrier” which may be interchangeably used refer to a carrier or a diluent that does not cause significant irritation to an organism and does not abrogate the biological activity and properties of the administered compound. An adjuvant is included under these phrases.
Herein the term “excipient” refers to an inert substance added to a pharmaceutical composition to further facilitate administration of an active ingredient. Examples, without limitation, of excipients include calcium carbonate, calcium phosphate, various sugars and types of starch, cellulose derivatives, gelatin, vegetable oils and polyethylene glycols.
Techniques for formulation and administration of drugs may be found in “Remington's Pharmaceutical Sciences,” Mack Publishing Co., Easton, Pa., latest edition, which is incorporated herein by reference.
Suitable routes of administration may, for example, include oral, rectal, transmucosal, especially transnasal, intestinal or parenteral delivery, including intramuscular, subcutaneous and intramedullary injections as well as intrathecal, direct intraventricular, intracardiac, e.g., into the right or left ventricular cavity, into the common coronary artery, intravenous, intraperitoneal, intranasal, or intraocular injections.
Alternately, one may administer the pharmaceutical composition in a local rather than systemic manner, for example, via injection of the pharmaceutical composition directly into a tissue region of a patient.
The term “tissue” refers to part of an organism consisting of cells designed to perform a function or functions. Examples include, but are not limited to, brain tissue, retina, skin tissue, hepatic tissue, pancreatic tissue, bone, cartilage, connective tissue, blood tissue, muscle tissue, cardiac tissue brain tissue, vascular tissue, renal tissue, pulmonary tissue, gonadal tissue, hematopoietic tissue.
Pharmaceutical compositions of some embodiments of the invention may be manufactured by processes well known in the art, e.g., by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or lyophilizing processes.
Pharmaceutical compositions for use in accordance with some embodiments of the invention thus may be formulated in conventional manner using one or more physiologically acceptable carriers comprising excipients and auxiliaries, which facilitate processing of the active ingredients into preparations which, can be used pharmaceutically. Proper formulation is dependent upon the route of administration chosen.
For injection, the active ingredients of the pharmaceutical composition may be formulated in aqueous solutions, preferably in physiologically compatible buffers such as Hank's solution, Ringer's solution, or physiological salt buffer. For transmucosal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art.
For oral administration, the pharmaceutical composition can be formulated readily by combining the active compounds with pharmaceutically acceptable carriers well known in the art. Such carriers enable the pharmaceutical composition to be formulated as tablets, pills, dragees, capsules, liquids, gels, syrups, slurries, suspensions, and the like, for oral ingestion by a patient.
Dragee cores are provided with suitable coatings. For this purpose, concentrated sugar solutions may be used which may optionally contain gum arabic, talc, polyvinyl pyrrolidone, carbopol gel, polyethylene glycol, titanium dioxide, lacquer solutions and suitable organic solvents or solvent mixtures. Dyestuffs or pigments may be added to the tablets or dragee coatings for identification or to characterize different combinations of active compound doses.
Pharmaceutical compositions which can be used orally, include push-fit capsules made of gelatin as well as soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol. The push-fit capsules may contain the active ingredients in admixture with filler such as lactose, binders such as starches, lubricants such as talc or magnesium stearate and, optionally, stabilizers. In soft capsules, the active ingredients may be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols. In addition, stabilizers may be added. All formulations for oral administration should be in dosages suitable for the chosen route of administration.
For buccal administration, the compositions may take the form of tablets or lozenges formulated in conventional manner.
The pharmaceutical composition described herein may be formulated for parenteral administration, e.g., by bolus injection or continuous infusion. Formulations for injection may be presented in unit dosage form, e.g., in ampoules or in multidose containers with optionally, an added preservative. The compositions may be suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents.
Pharmaceutical compositions for parenteral administration include aqueous solutions of the active preparation in water-soluble form. Additionally, suspensions of the active ingredients may be prepared as appropriate oily or water based injection suspensions.
Pharmaceutical compositions suitable for use in context of some embodiments of the invention include compositions wherein the active ingredients are contained in an amount effective to achieve the intended purpose. More specifically, a therapeutically effective amount means an amount of active ingredient (a conjugate as described herein) effective to prevent, alleviate or ameliorate symptoms of a disorder (e.g., as described herein) or prolong the survival of the subject being treated.
Determination of a therapeutically effective amount is well within the capability of those skilled in the art, especially in light of the detailed disclosure provided herein.
For any preparation used in the methods of the invention, the therapeutically effective amount or dose can be estimated initially from in vitro and cell culture assays. For example, a dose can be formulated in animal models to achieve a desired concentration or titer. Such information can be used to more accurately determine useful doses in humans.
Toxicity and therapeutic efficacy of the active ingredients described herein can be determined by standard pharmaceutical procedures in vitro, in cell cultures or experimental animals. The data obtained from these in vitro and cell culture assays and animal studies can be used in formulating a range of dosage for use in human. The dosage may vary depending upon the dosage form employed and the route of administration utilized. The exact formulation, route of administration and dosage can be chosen by the individual physician in view of the patient's condition. (See e.g., Fingl, et al., 1975, in “The Pharmacological Basis of Therapeutics”, Ch. 1 p. 1).
The amount of a composition to be administered will, of course, be dependent on the subject being treated, the severity of the affliction, the manner of administration, the judgment of the prescribing physician, etc.
Compositions of some embodiments of the invention may, if desired, be presented in a pack or dispenser device, such as an FDA approved kit, which may contain one or more unit dosage forms containing the active ingredient. The pack may, for example, comprise metal or plastic foil, such as a blister pack. The pack or dispenser device may be accompanied by instructions for administration. The pack or dispenser may also be accommodated by a notice associated with the container in a form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals, which notice is reflective of approval by the agency of the form of the compositions or human or veterinary administration. Such notice, for example, may be of labeling approved by the U.S. Food and Drug Administration for prescription drugs or of an approved product insert. Compositions comprising a preparation of the invention formulated in a compatible pharmaceutical carrier may also be prepared, placed in an appropriate container, and labeled for treatment of an indicated condition, as is further detailed above.
The composition may further comprise an additional therapeutically active agent usable in treating an indicated condition, as described herein.
General:
The term “treating” refers to inhibiting, preventing or arresting the development of a pathology (disease, disorder or condition) and/or causing the reduction, remission, or regression of a pathology. Those of skill in the art will understand that various methodologies and assays can be used to assess the development of a pathology, and similarly, various methodologies and assays may be used to assess the reduction, remission or regression of a pathology.
As used herein, the term “preventing” refers to keeping a disease, disorder or condition from occurring in a subject who may be at risk for the disease, but has not yet been diagnosed as having the disease.
As used herein, the term “subject” includes mammals, preferably human beings at any age which suffer from the pathology. Preferably, this term encompasses individuals who are at risk to develop the pathology.
It is expected that during the life of a patent maturing from this application many relevant RNA silencing agents will be developed and the scope of the term “RNA silencing agent” is intended to include all such new technologies a priori.
As used herein the term “about” refers to ±10%, or to ±5%.
The terms “comprises”, “comprising”, “includes”, “including”, “having” and their conjugates mean “including but not limited to”.
The term “consisting of” means “including and limited to”.
The term “consisting essentially of” means that the composition, method or structure may include additional ingredients, steps and/or parts, but only if the additional ingredients, steps and/or parts do not materially alter the basic and novel characteristics of the claimed composition, method or structure.
As used herein, the singular form “a”, “an” and “the” include plural references unless the context clearly dictates otherwise. For example, the term “a compound” or “at least one compound” may include a plurality of compounds, including mixtures thereof.
Throughout this application, various embodiments of this invention may be presented in a range format. It should be understood that the description in range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the invention. Accordingly, the description of a range should be considered to have specifically disclosed all the possible subranges as well as individual numerical values within that range. For example, description of a range such as from 1 to 6 should be considered to have specifically disclosed subranges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numbers within that range, for example, 1, 2, 3, 4, 5, and 6. This applies regardless of the breadth of the range.
Whenever a numerical range is indicated herein, it is meant to include any cited numeral (fractional or integral) within the indicated range. The phrases “ranging/ranges between” a first indicate number and a second indicate number and “ranging/ranges from” a first indicate number “to” a second indicate number are used herein interchangeably and are meant to include the first and second indicated numbers and all the fractional and integral numerals therebetween.
As used herein the term “method” refers to manners, means, techniques and procedures for accomplishing a given task including, but not limited to, those manners, means, techniques and procedures either known to, or readily developed from known manners, means, techniques and procedures by practitioners of the chemical, pharmacological, biological, biochemical and medical arts.
When reference is made to particular sequence listings, such reference is to be understood to also encompass sequences that substantially correspond to its complementary sequence as including minor sequence variations, resulting from, e.g., sequencing errors, cloning errors, or other alterations resulting in base substitution, base deletion or base addition, provided that the frequency of such variations is less than 1 in 50 nucleotides, alternatively, less than 1 in 100 nucleotides, alternatively, less than 1 in 200 nucleotides, alternatively, less than 1 in 500 nucleotides, alternatively, less than 1 in 1000 nucleotides, alternatively, less than 1 in 5,000 nucleotides, alternatively, less than 1 in 10,000 nucleotides.
As used herein, the term “alkyl” describes an aliphatic hydrocarbon including straight chain and branched chain groups. Preferably, the alkyl group has 1 to 20 carbon atoms, and more preferably 1 to 10 carbon atoms. Whenever a numerical range; e.g., “1 to 10”, is stated herein, it implies that the group, in this case the alkyl group, may contain 1 carbon atom, 2 carbon atoms, 3 carbon atoms, etc., up to and including 10 carbon atoms.
In the context of the present invention, a “long alkyl” is an alkyl having at least 10 carbon atoms in its main chain (the longest path of continuous covalently attached atoms). In the context of the present invention, a “medium alkyl” is an alkyl having from 5 to 9 carbon atoms in its main chain (the longest path of continuous covalently attached atoms). A short alkyl therefore has 4 or less main-chain carbons. The alkyl can be substituted or unsubstituted. When substituted, the substituent can be, for example, an alkyl, an alkenyl, an alkynyl, a cycloalkyl, an aryl, a heteroaryl, a halide, an amine, a hydroxyl, a thiol, an alkoxy and a thioalkoxy, as these terms are defined herein.
The alkyl group can be an end group, as this phrase is defined hereinabove, wherein it is attached to a single adjacent atom, or a linking group, as this phrase is defined hereinabove, which connects two or more moieties via at least two carbons in its chain. When the alkyl is a linking group, it is also referred to herein as “alkylene” or “alkylene chain”.
The term “alkenyl” describes an unsaturated alkyl, as defined herein, having at least two carbon atoms and at least one carbon-carbon double bond. The alkenyl may be substituted or unsubstituted by one or more substituents, as described hereinabove.
The term “alkynyl”, as defined herein, is an unsaturated alkyl having at least two carbon atoms and at least one carbon-carbon triple bond. The alkynyl may be substituted or unsubstituted by one or more substituents, as described hereinabove.
The term “heteroalicyclic” describes a monocyclic or fused ring group having in the ring(s) one or more atoms such as nitrogen, oxygen and sulfur. The rings may also have one or more double bonds. However, the rings do not have a completely conjugated pi-electron system. The heteroalicyclic may be substituted or unsubstituted. Substituted heteroalicyclic may have one or more substituents, whereby each substituent group can independently be, for example, hydroxyalkyl, trihaloalkyl, cycloalkyl, alkenyl, alkynyl, aryl, heteroaryl, heteroalicyclic, amine, halide, hydroxy, alkoxy and thioalkoxy. Representative examples are piperidine, piperazine, tetrahydrofurane, tetrahydropyrane, morpholino and the like.
Piperidine and piperazine are exemplary nitrogen-containing heterocylic.
The term “hydroxy”, as used herein, refers to an —OH group.
The term “alkoxy” refers to a —OR′ group, were R′ is alkyl, aryl, heteroalicyclic or heteroaryl.
As used herein, the term “amine” describes a —NR′R″ group where each of R′ and R″ is independently hydrogen, alkyl, cycloalkyl, heteroalicyclic, aryl or heteroaryl, as these terms are defined herein.
The term “aryl” describes an all-carbon monocyclic or fused-ring polycyclic (i.e., rings which share adjacent pairs of carbon atoms) groups having a completely conjugated pi-electron system. The aryl group may be substituted or unsubstituted by one or more substituents, as described hereinabove.
The term “heteroaryl” describes a monocyclic or fused ring (i.e., rings which share an adjacent pair of atoms) group having in the ring(s) one or more atoms, such as, for example, nitrogen, oxygen and sulfur and, in addition, having a completely conjugated pi-electron system. Examples, without limitation, of heteroaryl groups include pyrrole, furane, thiophene, imidazole, oxazole, thiazole, pyrazole, pyridine, pyrimidine, quinoline, isoquinoline and purine. The heteroaryl group may be substituted or unsubstituted by one or more substituents, as described hereinabove. Representative examples of nitrogen-containing heterocyclics include imidazole, thiadiazole, pyridine, pyrrole, oxazole, indole, purine and the like.
As used herein, the terms “halo” and “halide”, which are referred to herein interchangeably, describe an atom of a halogen, that is fluorine, chlorine, bromine or iodine, also referred to herein as fluoride, chloride, bromide and iodide.
The term “haloalkyl” describes an alkyl group as defined above, further substituted by one or more halide(s).
The term “alkylene” as used herein describes a —(CR′R″)f-, wherein R′ and R″ are as described herein, and f is an integer from 1 to 20, or from 1 to 10.
The term “thiol” describes a —SH group.
The term “thioalkoxy” describes both an —S-alkyl group, and an —S-cycloalkyl group, as defined herein.
The term “cyano” describes a —C—N group.
The term “carbonyl” describes a —C(═O)—R′ group, where R′ is hydrogen, alkyl, cycloalkyl, aryl, heteroaryl (bonded through a ring carbon) or heteroalicyclic (bonded through a ring carbon) as defined herein.
The term “thiocarbonyl” describes a —C(═S)—R′ group, where R′ is as defined herein.
The term “O-carbamyl” describes an —OC(═O)—NR′R″ group, where R′ is as defined herein and R″ is hydrogen, alkyl, cycloalkyl, aryl, heteroaryl (bonded through a ring carbon) or heteroalicyclic (bonded through a ring carbon) as defined herein.
The term “N-carbamyl” describes an R′OC(═O)—NR″— group, where R′ and R″ are as defined herein.
The term “O-thiocarbamyl” describes an —OC(═S)—NR′R″ group, where R′ and R″ are as defined herein.
The term “N-thiocarbamyl” describes an R″OC(═S)NR′— group, where R′ and R″ are as defined herein.
The term “amide” describes a —C(═O)—NR′R″ group, where R′ and R″ are as defined herein.
The term “carboxy” describes a —C(═O)—O—R′ groups, where R′ is as defined herein. When R′ is H, this term is also referred to herein as carboxylic acid. When R′ is alkyl, cycloalkyl or aryl, this term is also referred to herein as carboxylate.
The term “sulfonyl” group describes an —S(═O)2—R′ group, where R′ is as defined herein.
The term “halogen” or “halo” describes fluoro, chloro, bromo or iodo atom.
As used herein, the term “amine” describes both a —NR′R″ group and a —NR′— group, wherein R′ and R″ are each independently hydrogen, alkyl, cycloalkyl, aryl, as these terms are defined hereinbelow.
The amine group can therefore be a primary amine, where both R′ and R″ are hydrogen, a secondary amine, where R′ is hydrogen and R″ is alkyl, cycloalkyl or aryl, or a tertiary amine, where each of R′ and R″ is independently alkyl, cycloalkyl or aryl. Alternatively, R′ and R″ can each independently be hydroxyalkyl, trihaloalkyl, cycloalkyl, alkenyl, alkynyl, aryl, heteroaryl, heteroalicyclic, amine, halide, sulfonate, sulfoxide, phosphonate, hydroxy, alkoxy, aryloxy, thiohydroxy, thioalkoxy, thioaryloxy, cyano, nitro, azo, sulfonamide, carbonyl, C-carboxylate, O-carboxylate, N-thiocarbamate, O-thiocarbamate, urea, thiourea, N-carbamate, O-carbamate, C-amide, N-amide, guanyl, guanidine and hydrazine.
The term “amine” is used herein to describe a —NR′R″ group in cases where the amine is an end group, as defined hereinunder, and is used herein to describe a —NR′— group in cases where the amine is a linking group.
Herein throughout, the phrase “end group” describes a group (a substituent) that is attached to another moiety in the compound via one atom thereof.
The phrase “linking group” describes a group (a substituent) that is attached to another moiety in the compound via two or more atoms thereof.
Herein, the phrase “therapeutically active agent” is also referred to herein as “drug”.
The polymeric moieties described herein may possess asymmetric carbon atoms (optical centers) or double bonds; the racemates, diastereomers, geometric isomers and individual isomers are encompassed within the scope of the present invention.
As used herein, the term “enantiomer” describes a stereoisomer of a compound that is superposable with respect to its counterpart only by a complete inversion/reflection (mirror image) of each other. Enantiomers are said to have “handedness” since they refer to each other like the right and left hand. Enantiomers have identical chemical and physical properties except when present in an environment which by itself has handedness, such as all living systems.
The polymeric moieties described herein can exist in unsolvated forms as well as solvated forms, including hydrated forms. In general, the solvated forms are equivalent to unsolvated forms and are encompassed within the scope of the present invention.
The term “solvate” refers to a complex of variable stoichiometry (e.g., di-, tri-, tetra-, penta-, hexa-, and so on), which is formed by a solute (the conjugate described herein) and a solvent, whereby the solvent does not interfere with the biological activity of the solute. Suitable solvents include, for example, ethanol, acetic acid and the like.
The term “hydrate” refers to a solvate, as defined hereinabove, where the solvent is water.
As used herein, a “reactive group” describes a chemical group that is capable of reacting with another group so as to form a chemical bond, typically a covalent bond. Optionally, an ionic or coordinative bond is formed.
A reactive group is termed as such if being chemically compatible with a reactive group of an agent or moiety that should be desirably attached thereto. For example, a carboxylic group is a reactive group suitable for conjugating an agent or a moiety that terminates with an amine group, and vice versa.
A reactive group can be inherently present in the monomeric units forming the backbone units, or be generated therewithin by terms of chemical modifications of the chemical groups thereon or by means of attaching to these chemical groups a spacer or a linker that terminates with the desired reactive group.
By “cancer” are encompassed any solid or non-solid cancer and/or cancer metastasis, including, but is not limiting to, tumors of the gastrointestinal tract (colon carcinoma, rectal carcinoma, colorectal carcinoma, colorectal cancer, colorectal adenoma, hereditary nonpolyposis type 1, hereditary nonpolyposis type 2, hereditary nonpolyposis type 3, hereditary nonpolyposis type 6; colorectal cancer, hereditary nonpolyposis type 7, small and/or large bowel carcinoma, esophageal carcinoma, tylosis with esophageal cancer, stomach carcinoma, pancreatic carcinoma, pancreatic endocrine tumors), endometrial carcinoma, dermatofibrosarcoma protuberans, gallbladder carcinoma, Biliary tract tumors, prostate cancer, prostate adenocarcinoma, renal cancer (e.g., Wilms' tumor type 2 or type 1), liver cancer (e.g., hepatoblastoma, hepatocellular carcinoma, hepatocellular cancer), bladder cancer, embryonal rhabdomyosarcoma, germ cell tumor, trophoblastic tumor, testicular germ cells tumor, immature teratoma of ovary, uterine, epithelial ovarian, sacrococcygeal tumor, choriocarcinoma, placental site trophoblastic tumor, epithelial adult tumor, ovarian carcinoma, serous ovarian cancer, ovarian sex cord tumors, cervical carcinoma, uterine cervix carcinoma, small-cell and non-small cell lung carcinoma, nasopharyngeal, breast carcinoma (e.g., ductal breast cancer, invasive intraductal breast cancer, sporadic; breast cancer, susceptibility to breast cancer, type 4 breast cancer, breast cancer-1, breast cancer-3; breast-ovarian cancer), squamous cell carcinoma (e.g., in head and neck), neurogenic tumor, astrocytoma, ganglioblastoma, neuroblastoma, lymphomas (e.g., Hodgkin's disease, non-Hodgkin's lymphoma, B cell, Burkitt, cutaneous T cell, histiocytic, lymphoblastic, T cell, thymic), gliomas, adenocarcinoma, adrenal tumor, hereditary adrenocortical carcinoma, brain malignancy (tumor), various other carcinomas (e.g., bronchogenic large cell, ductal, Ehrlich-Lettre ascites, epidermoid, large cell, Lewis lung, medullary, mucoepidermoid, oat cell, small cell, spindle cell, spinocellular, transitional cell, undifferentiated, carcinosarcoma, choriocarcinoma, cystadenocarcinoma), ependimoblastoma, epithelioma, erythroleukemia (e.g., Friend, lymphoblast), fibrosarcoma, giant cell tumor, glial tumor, glioblastoma (e.g., multiforme, astrocytoma), glioma hepatoma, heterohybridoma, heteromyeloma, histiocytoma, hybridoma (e.g., B cell), hypernephroma, insulinoma, islet tumor, keratoma, leiomyoblastoma, leiomyosarcoma, leukemia (e.g., acute lymphatic, acute lymphoblastic, acute lymphoblastic pre-B cell, acute lymphoblastic T cell leukemia, acute—megakaryoblastic, monocytic, acute myelogenous, acute myeloid, acute myeloid with eosinophilia, B cell, basophilic, chronic myeloid, chronic, B cell, eosinophilic, Friend, granulocytic or myelocytic, hairy cell, lymphocytic, megakaryoblastic, monocytic, monocytic-macrophage, myeloblastic, myeloid, myelomonocytic, plasma cell, pre-B cell, promyelocytic, subacute, T cell, lymphoid neoplasm, predisposition to myeloid malignancy, acute nonlymphocytic leukemia), lymphosarcoma, melanoma, mammary tumor, mastocytoma, medulloblastoma, mesothelioma, metastatic tumor, monocyte tumor, multiple myeloma, myelodysplastic syndrome, myeloma, nephroblastoma, nervous tissue glial tumor, nervous tissue neuronal tumor, neurinoma, neuroblastoma, oligodendroglioma, osteochondroma, osteomyeloma, osteosarcoma (e.g., Ewing's), papilloma, transitional cell, pheochromocytoma, pituitary tumor (invasive), plasmacytoma, retinoblastoma, rhabdomyosarcoma, sarcoma (e.g., Ewing's, histiocytic cell, Jensen, osteogenic, reticulum cell), schwannoma, subcutaneous tumor, teratocarcinoma (e.g., pluripotent), teratoma, testicular tumor, thymoma and trichoepithelioma, gastric cancer, fibrosarcoma, glioblastoma multiforme; multiple glomus tumors, Li-Fraumeni syndrome, liposarcoma, lynch cancer family syndrome II, male germ cell tumor, mast cell leukemia, medullary thyroid, multiple meningioma, endocrine neoplasia myxosarcoma, paraganglioma, familial nonchromaffin, pilomatricoma, papillary, familial and sporadic, rhabdoid predisposition syndrome, familial, rhabdoid tumors, soft tissue sarcoma, and Turcot syndrome with glioblastoma.
It is appreciated that certain features of the invention, which are, for clarity, described in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features of the invention, which are, for brevity, described in the context of a single embodiment, may also be provided separately or in any suitable subcombination or as suitable in any other described embodiment of the invention. Certain features described in the context of various embodiments are not to be considered essential features of those embodiments, unless the embodiment is inoperative without those elements.
Various embodiments and aspects of the present invention as delineated hereinabove and as claimed in the claims section below find experimental support in the following examples.
Reference is now made to the following examples, which together with the above descriptions illustrate some embodiments of the invention in a non limiting fashion.
All chemicals and solvents were A.R. or HPLC grade. Chemical reagents were purchased from Sigma-Aldrich (Israel) and Merck (Israel). O-benzyl protected glutamic acid (H-Glu(OBzl)-OH) were purchased from Chemimpex (Israel). HPLC grade solvents were from Biolab (Israel). All tissue culture reagents were purchased from Biological Industries Ltd (Beit Haemek, Israel), unless otherwise indicated.
All tissue culture reagents were purchased from Biological Industries Ltd (Beit Haemek, Israel), unless otherwise indicated.
EGFP siRNA, Rac1 siRNA, Cy5-labeled Rac1 siRNA, Plk1 siRNA sequences were obtained from collaborators.
Aminated PGA polymers were prepared as described in Example 1 hereinunder.
1H-Nuclear Magnetic Resonance (NMR):
NMR spectroscopy was performed by 400 MHz Avacne, Bruker (Karlshruhe, Germany) system. PGAamine was dissolved in D2O.
Gel Permeation Chromatography (GPC):
GPC Max VE2001 system (Viscotek) was used for size analysis of the OBz-PGA, equipped with VE3580 RI detector and OmniSEC 4.7 software. 4 columns of Styragel (Waters), HR 4, 3, 1, 0.5 were used in a raw. Chromatographic conditions: flow: 0.5 ml/min, isocratic DMF supplemented with 0.1 M LiBr. 3 OBz-PGA standards (Alamanda, 11 KDa, 22 KDa and 44 KDa) were used for size calibration.
Electrophoretic Mobility Shift Assay (EMSA):
Evaluation of siRNA: polymer complexation in molar ratios between 1:1 to 15:1 (N/P ratios) was performed as follows: 50 pmol of siRNA and increasing amount of polymer were diluted in RNase free water, mixed together and left to form complexes at room temperature for 20-30 minutes. DNA loading buffer was added to the samples, and the solution was loaded on a 2% agarose gel supplemented with ethidium bromide. A voltage of 100 volts was applied for 30 minutes. Sample's run was evaluated under UV light.
Zeta Potential Determination:
The zeta-potential measurements were performed using a ZetaSizer Nano ZS instrument with an integrated 4 mW He—Ne laser (λ=633 nm; Malvern Instruments Ltd., Malvern, Worcestershire, UK). PGAamine:siRNA samples were prepared by dissolving 1 mg of polymer and the indicated amount of siRNA (diluted from 20 μM Rac1-siRNA in RNase free water solution) in 1 ml of 15 mM phosphate buffer, pH=7.4. All measurements were performed at 25° C. using folded capillary cell (DTS 1070) for zeta-potential measurements.
Dynamic Light Scattering:
The hydrodynamic radius and PDI measurements were performed using either a ZetaSizer Nano ZS instrument with an integrated 4 mW He—Ne laser (λ=633 nm; Malvern Instruments Ltd., Malvern, Worcestershire, UK), or Vasco DLS (Nano Instruments Ltd. Cordouan Technologies, Pessac, France), equipped with a 657 nm laser. Data analysis was performed according to cumulants analysis. All measurements were performed at 25° C.
Nanoparticles Tracking Analysis (NTA):
Polyplexes for NTA were prepared as followed: PGAamine polymer was dissolved in DDW to 0.1 mg/mL solution. RNA was added at the indicated N/P ratio from a 20 μM solution in DDW. NTA Analysis was performed using a NanoSight NS300 (Malvern Instruments Ltd., Malvern, Worcestershire, UK), equipped with a sCMOS camera and a 532 nm laser. Data analysis was performed using NTA 3.1 software. Each sample was measured for 60 seconds at 3 different fields, measurements were taken at room temperature.
Multi Static Light Scattering (MALS):
Molecular weight and polydispersity analysis were performed on Agilent 1200 series HPLC system (Agilent Technologies) equipped with a multi angle light scattering detector (Dawn Heleos, Wyatt), using Shodex Kw404-4F column (Showa Denko America, Inc.) in PBS, flow 0.3 mL/minute for the polyglutamic acid. For the Polypexes, Shodex SB-803 HQ column was used in 0.5 M AcOH and 0.2 M sodium nitrate at flow 0.5 mL/min.
Scanning Electron Microscope:
Polymer solution at 0.1 mg/mL was mixed with siRNA solution at the indicated N/P ratio and incubated at room temperature for 20 minutes. Samples were filtered to remove large aggregates, dropped on a silicon wafer and blotted with cellulose paper.
SEM images were taken by Quanta 200 FEG Environmental SEM (FEI, Oreg., USA). Diameters were measured by measureIT software, Gaussian distribution was fitted using OriginPro software.
Transmission Electron Microscopy (TEM and Cryo-TEM).
Polymer solution was mixed with siRNA solution at 1.5 N/P ratio and 1.5 mg/kg equivalent siRNA concentration in 5% glucose solution. Polymer solution was prepared at the same concentration in 5% glucose solution. The resulting solutions were diluted in DDW to 0.5 mg/mL concentration, dropped on TEM GRID and negatively stained with uranyl acetate (for TEM imaging) or frozen (for Cryo-TEM imaging). TEM images were taken using JEM 1200EX TEM (JEOL Ltd., Tokyo, Japan). Cryo-TEM images were taken using Tecnai 12 TWIN TEM (FEI, Oreg., USA). Radiuses were measured by measureIT software and represent the average of 3 fields, 40 particles per field.
Flow Cytometry (FACS).
HeLa and SKOV-3 cells were seeded onto 6 wells plate at 200,000 cells/well densities. Following 24 h, cells were treated with PGAamine: Rac1 Cy5-labeled siRNA for 4 h. Cells were washed twice with PBS, and harvested with phenol red free Trypsin. 3 mL of 5% FBS in PBS solution were added, and the samples were centrifuged for 7 min at 1100 rpm. Supernatant was discharged, and cells pellets were suspended in 500 μL of 5% FBS in PBS solution. Fluorescence was read at 635 nm using FACSCalibur™ flow cytometer (BD Biosciences, Heidelberg, Germany).
Confocal:
Cells uptake of the PGAamine:Cy5-Rac1 siRNA polyplexes was followed using Leica SP5 confocal imaging systems (X60 Magnification). HeLa cells were treated with polyplexes of PGAamines A to I and Cy5-Rac1 siRNA for various time courses. The cells were fixed with 4% paraformaldehyde and stained with mouse anti EEA1 (BD) and with rabbit anti LAMP1 (Cell signaling) primary antibodies, and then with Goat anti mouse IgG-FITC and Goat anti rabbit IgG-Rhodamine secondary antibodies.
Luciferase Reporter Assay:
In vitro silencing of Rac gene/PLK1 gene by siRac1-polyplex/siPLK1-polyplex was evaluated using psiCHECK reporter assay (Promega Cat No. E1960 Madison, Wis., USA). psiCHECK™-2-based (Promega) construct was prepared for the evaluation of the target activity of Rac1/Plk1. One copy of a consensus target sequence of Rac1/PLK1 was cloned into the multiple cloning site located downstream of the Renilla luciferase translational stop codon in the 3′-UTR region.
HeLa cells (1×106) were seeded in 10 cm dishes and were incubated in a 37° C., 5% CO2 incubator for 24 hours. Each cell-containing plate was transfected with 4 μg Rac1-psiCHECK™-2-based plasmids using 4 μL Lipofectamine® 2000 (Life Technologies, Grand Island, N.Y.). Following 5 hours, cells were re-seeded in 96-wells plate at final concentration of 4000 cells per well and incubated overnight.
Cells expressing siRNA reporter plasmid were transfected with Rac1/Plk1 siRNA or eGFP/Luciferase siCtrl either complexed with PGA cationic carrier or with Lipofectamine® 2000 as a control (100, 250, or 500 nM siRNA;) or left untreated.
After 72 hours, medium was removed completely from cells and the cells were lysed for 20 minutes in room temperature in gentle rocking by the addition of 50 μL/well 1× Luciferase lysis solution. Renilla and firefly luciferase activities were measured in each of the wells of the 96-wells plate, using Dual-Luciferase® Assay kit (Promega Corporation, Wisconsin, USA) according to manufacturer procedure. Aliquots of 10 μL of cell lysate from each sample were transferred to a 96-well white plate. Forty L of Luciferase substrate (LARII) was added to each extract and firefly luciferase activity was measured by luminescence microplate Reader (Mithras LB 940 Multimode Microplate Reader, Berthold Technologies, Germany), then 40 μL of Stop&Glo Reagent was added to each of the samples and Renilla luciferase activity was measured immediately afterwards. The Renilla luciferase activity is expressed as the percentage of the normalized activity value (Renilla luciferase/firefly luciferase) in the tested sample relative to the normalized value obtained in cells transfected with the corresponding psiCHECK™-2 plasmid only (no siRNA or polyplex).
Cells Viability Assay:
HeLa cells were plated onto a 96-well plate (4000 cells/well) in DMEM supplemented with 10% FBS, 2 mM L-glutamine and incubated for 24 hours (37° C.; 5% CO2). Then, cells were transfected with siRNA complexed with PGAamine in various N/P ratios, at 100-500 nM-Rac1/EGFP siRNA concentration or 50 nM Rac1/EGFP siRNA transfected by Lipofectamine™ 2000 as positive control. Following 72 hours amount of viable cells was assessed by modified 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolinium bromide (MTT) assay. Thirty L of 3 mg/ml MTT solution in PBS were added to the wells and incubated for 4-6 hours, the medium was then replaced by 200 μL of dimethyl sulfoxide (DMSO) to dissolve the formazan crystals formed, incubated for 20 minutes at 37° C. Absorbance of the solution was measured at 560 nm by SpectraMax® M5 plate reader (molecular devices). Percent of viable cells was normalized to the viability of non-treated cells (100% viability).
Heparin Displacement Assay.
The relative strength of complexation of PGAamine:siRNA polyplexes was evaluated by measuring the release of siRNA in the presence of heparin. PGAamine:siRNA polyplexes were prepared as described herein. Polyplex solutions were incubated in the presence of 0.01-0.35 IU of heparin/50 pmol siRNA for 15 minutes. DNA loading buffer was added to the samples, and the samples were loaded on a 2% agarose gel supplemented with ethidium bromide. A voltage of 100 volts was applied for 15-30 minutes. Sample's run was evaluated under UV light.
Monolayer Wound Healing Assay.
To study the ability of PGAamine:siRac1 polyplex to inhibit the migration of SKOV-3 cells, IncuCyte ZOOM® Live Cell Imaging system (Essen BioScience, Ann Arbor, Mich., USA) was used.
SKOV-3 cells were plated onto a 96-well ImageLock tissue culture plate (Essen BioScience, Ann Arbor, Mich., USA) (30,000 cells/well) in DMEM supplemented with 10% FBS, 2 mM L-glutamine and incubated for 24 hours (37° C.; 5% CO2). Using WoundMaker™, a precise gap was made in each well of 96-wells plate, dislodged cells were washed with DMEM medium. Next, cells were treated with 500 nM siRNA (Rac1 or Ctrl) complexed with PGAamine, with siRac1 only or left untreated with medium only. The plate was placed in IncuCyte ZOOM™ incubator and phase contrast images were taken at regular intervals over a course of 19 hours by IncuCyte ZOOM™ CellPlayer using 10× objective. Relative Wound Density (RWD) accounts for the background density of the wound at the initial time point, and for changes in both the density of the cell (outside the wound region) and the wound region. This parameter is calculated and graphically presented by the IncuCyte™ Software.
Plasma Stability Assay.
The stability of siRac1-polyplex in plasma was evaluated by incubating the polyplexes in whole mouse plasma/fetal bovine serum (FBS) for 0.25-24 hours. Following incubation, the samples were divided to two; one half was incubated for additional 15 minutes with heparin (0.21 IU of heparin/35 pmol siRNA) and the other was incubated in Ultra-Pure Water (UPW) for additional 15 minutes. Next, the samples were loaded on 2% agarose gel and electrophoresis was performed at 100 V for 15-30 minutes. The gel was stained with ethidium bromide solution for siRNA visualization under UV light. As control, naked siRNA at the same concentration as in the polyplexes was loaded into the gel.
Hemolysis Assay:
Rat red blood cells (RBC) solution (2% wt/wt) was incubated with serial dilutions of PGAamine:siRac1 polyplex for 1 hour at 37° C. Dextran (Mw 70 kDa, Sigma) or PBS were used as negative controls, whereas 1% wt/vol solution of Triton X-100 or SDS as positive control. Following centrifugation, the supernatants were transferred to a new plate and absorbance was measured at 550 nm using a SpectraMax® M5e plate reader (Molecular Devices LLC., Sunnyvale, Calif., USA).
Skov-3 Cells Migration Assay:
Cells migration assay was performed using modified 8 μm Boyden chambers. Prior to migration assay, Skov-3 cells were transfected with PGAamine:Rac1 siRNA polyplexes for 48 hours in 6-well plate (150,000 cells/well) in DMEM+20% FCS, 1% Hepes 1 M, 1% sodium pyruvate, 100 μg/mL Penicillin 100 U/mL Streptomycin, 2 mM L-glutamine. Then cells were washed and added without polyplexes to the upper chamber of the transwell (100,000 cells/well) in 100 μL of DMEM without FBS. Two hours later, cells were allowed to migrate to the underside of the chamber for another 20 hours, in the presence or absence of FBS (20% v/v) in the lower chamber. Cells were then fixated with ice-cold methanol and stained (Hema 3 Stain System). Next the stained and migrated cells were imaged using Nikon TE2000E inverted microscope by ×6 objective, brightfield illumination. Migrated cells from captured images were counted using NIH image software (ImageJ). Percent of migrated cells was normalized to migrated cells toward FBS alone (no siRNA transfection).
Western Blot Analysis:
MDA-MB-231 and MCF-7 cells were seeded in 6 wells plate at a density of 100,000 cells/well. After 24 hours, cells were treated with 250 nM of plk1/luciferase siRNA formulated with PGAamine or plk1 siRNA alone. Following 48 hours, cells were harvested and ran on an acryl amide gel under 120 V for about 2 hours. Gels were transferred to nitrocellulose membrane under 80 mA current for over-night. Membrane was blocked with 5% skim milk for 1 hour, reacted with rabbit anti-plk1 antibody (cell signaling) (1:500 in TBST) and mouse anti HSP70 antibody (Santa Cruz Biotechnology, Dallas, Tex., US) (1:40000) for over-night at 4° C., and then with Goat anti Rabbit and Goat anti mouse secondary antibodies (both at 1:10,000 in TBST) for 1 hour. Blots were developed using ECL kit (Thermo Fisher Scientific, Waltham, Mass., US) according to the manufacturer's protocol.
Growth Inhibition of MDA-MB-231 and MCF-7 Cells:
MDA-MB-231 cells were seeded in a 24 well plate at a density of 100,000 cells/well, while MCF-7 cells were seeded at a density of 70,000 cells/well. After 24 hours of incubation, cells were treated with PGAamine:Plk1 siRNA or PGAamine:Luciferase siRNA polyplexes in concentrations of 100, 250 and 500 nM. After 72 hours, cells were harvested and counted using coulter counter.
Maximum Tolerated Dose:
PGAamine:Rac1 siRNA polyplexes at N/P ratio of 5 (A, F and I) or 10 (B), at siRNA concentrations of 1-10 mg/kg were injected intravenously (i.v.) to BALB/c mice, at 400 μL/mouse. Mice were monitored for signs of toxicity up to 24 hours post injection.
MTD of PGAamine:Rac1 siRNA Polyplexes at 3, 5 and 10 N/P Ratios and of Alkylated PGAamine:Rac1 siRNA Polyplexes at 2 N/P:
PGAamine:Rac1 siRNA polyplexes at 3, 5 and 10 N/P ratio at siRNA concentrations of 2-10 mg/kg were injected i.v. to BALB/c mice, at 200 μL/mouse. Alkylated PGAamine:Rac1 siRNA polyplexes at 2 N/P ratio at siRNA concentrations of 8 and 15 mg/kg were injected i.v. to BALB/c mice, at 200 μL/mouse. Mice were monitored for signs of toxicity 24 hours post injection.
Anti-Cancer Efficacy of PGAamine:Plk1 siRNA/miR34a Polyplexes in Skov-3 mCherry-Labeled Orthotopic Tumor Bearing Nu/Nu Mice:
Nu/nu female mice were inoculated intraperitoneally (i.p.) with 6×106 mCherry-labeled Skov-3 human ovarian adenocarcinoma cells. Seven days post inoculation mice were monitored for tumor formation using CRI™ Maestro non-invasive intravital imaging system, according to the fluorescent measurements mice were randomized (n=7-8 mice/group). Tumor bearing mice were injected i.p. with polymer:siRNA (Plk1 or Luciferase) or polymer: miR (miR-34a or NC miR) formulations (9 q.o.d. injections of 8 mg/kg siRNA or miRNA equivalent dose), saline was injected to control mice (same treatment schedule).
Body weight and tumor progression was monitored twice a week. CRI Maestro™ non-invasive fluorescence imaging system was used to follow tumor progression of mice bearing mCherry-labeled tumors. Mice were anesthetized using ketamine (100 mg/kg) and xylazine (12 mg/kg) injected s.c. and placed inside the imaging system. Multispectral image-cubes were acquired through 550-800 nm spectral range in 10 nm steps using excitation (575-605 nm) and emission (645 nm longpass) filter set. Mice autofluorescence and undesired background signals were eliminated by spectral analysis and linear unmixing algorithm. At termination, tumors were dissected and weighed. Data is expressed as mean±standard error of the mean (s.e.m.).
Accumulation and Silencing Activity of PGAamine:siRac1/siLuc Polyplexes in A549 Lung Carcinoma SC Tumor Bearing Nu/Nu Mice:
Nu/nu female mice were subcutaneously (SC) inoculated with 4×106 A549 human lung carcinoma cells. When tumors reached 100 mm3 in size, twenty days post inoculation, mice were randomized (n=8 mice/group) and divided in a way that 1 group was used for PK study and the other for accumulation and silencing study. For PK study tumor bearing mice were injected once with PGAamine:siRac1 polyplexes or free siRac1 (4 mg/kg siRNA equivalent dose). Blood samples were collected at 0, 10, 30 minutes and 1, 2 and 24 hours, organs and tumors were collected as well at final time point. RAC 1 mRNA levels analysis in the RNA prepared from all frozen tumor tissues and cells were measured using qPCR. For siRNA detection the tissue was lysed and siRNA quantity examined by stem and loop qPCR technique.
PGAamine:siRac1 polyplex, PGAamine:siLuc polyplex Rac1 siRNA alone (4 mg/kg siRNA-equivalent dose) or saline were administered in 3 sequential IV injections (˜24 hours interval) in female nu/nu mice bearing SC lung tumors (n=8). Mice were euthanized 24 hours following the 3rd injection. Tumors were collected for analysis and were homogenized and lyophilized. Then, tissue lysates were prepared by placing the samples in 0.25% Triton X-100. The quantity of siRac1 was evaluated by stem-loop qPCR method using SYBR Green on Applied Biosystem 7300 PCR System.
Biodistribution of PGAamine:siRac1-Cy5 in mCherry Labelled MDA-MB-231 Mammary Adenocarcinoma Intramammary Tumor Bearing Nu/Nu Mice:
MDA-MB-231 cells were infected with the mCherry retroviral particles media, and 48 hours following the infection, mCherry positive cells were selected by puromycin resistance. Nu/nu female mice were intramammary inoculated with 1.5×106 mCherry MDA-MB-231 human breast carcinoma cells. When tumors reached 100 mm3 in size, 12 mice were injected with 1.5 mg/kg of PGAamine:siRac1-Cy5 and images were taken at specific time point (0, 3, 6 and 24 hours) with CRI™ Maestro non-invasive intravital imaging system. Mice were anesthetized using ketamine (100 mg/kg) and xylazine (12 mg/kg) injected s.c, and placed inside the imaging system. Multispectral image-cubes were acquired through 590-750 nm spectral range in 10 nm steps using excitation (605 nm) and emission (635 nm) filter set. Mice auto fluorescence and undesired background signals were eliminated by spectral analysis and the Maestro™ linear unmixing algorithm. After imaging, 3 mice at each time point were euthanized and organs resected to collect the images in the same conditions as reported above.
Accumulation and Silencing Activity of PGAamine:siRac1/siLuc Polyplexes in MDA-MB-231 Mammary Adenocarcinoma Intramammary Tumor Bearing Nu/Nu Mice:
Nu/nu female mice were intramammary inoculated with 1.5×106 MDA-MB-231 human breast carcinoma cells. When tumors reached 100 mm3 in size, twenty days post inoculation, mice were randomized (n=5 mice/group) and injected IV every day for 3 days with PGAamine:siRac1 polyplex, PGAamine:siLuc polyplex (1.5 mg/kg siRNA-equivalent concentration) or 5% glucose. Mice were euthanized 24 hours following the third injection. Tumors were collected for analysis and were homogenized and lyophilized. Then, tissue lysates were prepared by placing the samples in 0.25% Triton X-100. The quantity of siRac1 was evaluated by stem-loop qPCR method using SYBR Green on Applied Biosystem 7300 PCR System.
Aminated PGA polymers A to I (
The amine moieties conjugated to each polymeric backbone have varied in size and functionality: while Polymer A was conjugated to “short” side chain terminated by primary amine, Polymer B was conjugated to longer side chain. Polymer C was conjugated to side chain terminated by tertiary amine, which may increase the complexation strength with siRNA and decrease the N/P ratio of their complete complexation. Successful siRNA delivery depends on fine tuning between strong and stable complexation with the ability to release the siRNA to the cytoplasm before reaching the lysosome [Rejman, Bragonzi et al. 2005; Scomparin, Polyak et al. 2015)]. Polymers D and E were conjugated with two different moieties, each terminated by either primary or tertiary amine. This may achieve strong binding between the polymer and siRNA while maintain buffering capabilities ((Boussif, Lezoualc'h et al. 1995)). The effect of side chain's length on the size of these obtained polyplexes was evaluated by using either “short” (Polymer D) or longer (Polymer E) side chains. Polymer F was conjugated with a side chain bearing the two amine functionalities, combining terminal tertiary amine and medial secondary amine on the same side chain. In Polymer G, a combination of the latter side chain structure with side chain terminated by primary amine is present. Polymer H includes functionalities of primary and secondary amine on single side chain and Polymer I features a combination with tertiary and secondary amine on single side chain at a hybrid system.
Alkyl moiety-bearing aminated PGA polymers J to P (
Imidazole-bearing aminated PGA polymers Q and R (
Imidazole-bearing alkylated PGAamine polymers S and T (
Dialkylated PGAamine polymers U, V and W (
PGAamine polymers that bear amine moiety with tertiary and secondary amines and an alkyl moiety X and Y (
To a solution of poly-α-glutamic acid (50 mg, 0.38 mmol per monomer) in dry DMF (1 ml) was added a solution of Carbodiimidazole (75 mg, 0.46 mmol) in dry DMF (1 ml). The reaction, mixture was stirred for 1.5 hours, at 25° C., under Argon atmosphere. Tributylamine (94 μl, 0.39 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of Boc-Ethylenediamine (0.42 mmol) in dry DMF (1.5 mL) was added and the reaction mixture was stirred for additional 2 hours at the starting conditions. A solution of Carbodiimidazole (133 mg, 0.82 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred at 25° C., under Argon for additional 12 hours. DMF was removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH=5.5, then freeze dried. The remaining solid was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifluoraoacetic salt, with a 41% yield. 1H NMR (D2O; 400 MHz): δ 4.32 (1H, s), 3.45 (2H, s), 3.27 (2H, s), 2.36 (2H, s), 2.05, (1H, s), 1.94 (1H, s).
To a solution of poly-α-glutamic acid (50 mg, 0.38 mmol per monomer) in dry DMF (1 mL) was added a solution of Carbodiimidazole (192 mg, 1.20 mmol) in dry DMF (1 mL). The reaction mixture was stirred for 1.5 hours at 25° C., under nitrogen atmosphere. Tributylamine (92 μL, 0.39 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of Boc-1, 6-diaminohexane (1.96 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. DMF was removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 5.5, then freeze dried. The remaining solid was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifluoroacetic salt, with a 31% yield. 1H NMR (D2O; 400 MHz): δ 4.26 (1H, s), 3.13 (2H, s), 2.93 (2H, s), 2.32 (2H, s), 2.08, (1H, s), 1.97 (1H, s), 1.61 (2H, s), 1.47 (2H, s), 1.32 (4H, s).
To a solution of poly-α-glutamic acid (51 mg, 0.39 mmol per monomer) in dry DMF (1 mL) was added a solution of Carbodiimidazole (201 mg, 1.24 mmol) in dry DMF (1.5 mL). The reaction, mixture was stirred for 1.5 hours, at 25° C., under nitrogen atmosphere. Tributylamine (92 μL, 0.39 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of 3-(dimethylamine)-1-propylamine (3.98 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. Double distilled water (40 mL) was added and the mixture was treated with 10% HCl solution to pH of 2.5. The reaction mixture was extracted with CHCl3 (2×40 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to pH of 7, then freeze dried. The remaining solid was dissolved in double distilled water (20 mL) and dialyzed for 72 hours at 4° C. (total of 12 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a chloride salt, with a 45% yield. 1H NMR (D2O; 400 MHz): δ 4.29 (1H, s), 3.25 (2H, s), 3.01 (2H, s), 2.81 (6H, s), 2.33, (2H, s), 2.05-1.90 (2H, bs), 1.90 (2H, s).
To a solution of poly-α-glutamic acid (50 mg, 0.38 mmol per monomer) in dry DMF (1 mL) was added a solution of Carbodiimidazole (70 mg, 0.43 mmol) in dry DMF (1 mL). The reaction mixture was stirred for 1 hour, at 25° C., under nitrogen atmosphere. Tributylamine (92 μL, 0.39 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of 3-Dimethylamine-1-propylamine (0.12 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 1 hour at the starting conditions. A solution of Boc-ethylenediamine (0.31 mmol) in dry DMF was added and the reaction mixture was stirred for additional 2 hours at the starting conditions. A solution of Carbodiimidazole (125 mg, 0.477 mmol) in dry DMF (0.7 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. DMF was removed under reduced pressure. Double distilled water (40 mL) was added and the reaction mixture was freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 20 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 5.5, then freeze dried. The remaining solid was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifluoroacetic salt, with a 22% yield.
1H NMR (D2O; 400 MHz): δ 4.20 (1H, s), 4.04 (0.3H, s) 3.37 (2H, s), 3.15 (1H, s), 3.02 (2H, s), 2.76, (3H, s), 2.26 (3H, s), 1.98-1.81 (4H, bs).
To a solution of poly-α-glutamic acid (41 mg, 0.32 mmol per monomer) in dry DMF (2 ml) was added a solution of Carbodiimidazole (56 mg, 0.34 mmol) in dry DMF (1 mL). The reaction, mixture was stirred for 1 hour at 25° C., under nitrogen atmosphere. Tributylamine (83 μl, 0.32 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of 6-Dimethylhexyamine (0.09 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 1 hour at the starting conditions. A solution of Boc-diaminohexane (0.26 mmol) in dry DMF (1.5 mL) was added and the reaction mixture was stirred for additional 1 hour at the starting conditions. A solution of Carbodiimidazole (103 mg, 0.63 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. DMF was removed under reduced pressure. Double distilled water (40 mL) was added and the reaction mixture was freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 20 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 5.5, then freeze dried. The remaining solid was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifluoroacetic salt, with a 32% yield. 1H NMR (D2O; 400 MHz): δ 4.16 (1H, s), 3.03 (3H, s), 2.86 (1H, s), 2.73 (1H, s), 2.22 (2H, s), 1.98-1.86 (2H, bs), 1.53 (3H, s), 1.98 (3H, s), 1.23 (1H, s).
To a solution of poly-α-glutamic acid (40 mg, 0.31 mmol per monomer) in dry DMF (1 mL) was added a solution of Carbodiimidazole (60 mg, 0.37 mmol) in dry DMF (1 mL). The reaction, mixture was stirred for 1 hour at 25° C., under nitrogen atmosphere. Tributyl (73 μL, 0.31 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of Dimethyldipropylenetriamine (0.34 mmol) in dry DMF (2 mL) was added and the reaction mixture was stirred for additional 2 hours at the starting conditions. A solution of Carbodiimidazole (106 mg, 0.65 mmol) in dry DMF (2 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. Double distilled water (40 mL) was added and the reaction mixture was treated with 10% HCl solution to pH of 4. The reaction mixture was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 5.5, then freeze dried. The oil residue was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 6 L of double distilled water) and additional 12 hours at 25° C. (total of 2 L). The aqueous phase was collected and freeze dried to receive a white powder as a chloride salt, with a 35% yield. 1H NMR (D2O; 400 MHz): δ 4.27 (1H, s), 3.19 (3H, s), 2.59 (4H, s), 2.41 (2H, s), 2.33 (2H, s), 2.23 (6H, s), 2.08-1.97 (2H, bs), 1.67 (4H, s).
To a solution of poly-α-glutamic acid (41 mg, 0.32 mmol per monomer) in dry DMF (1 mL) was added a solution of Carbodiimidazole (57 mg, 0.34 mmol) in dry DMF (1 mL). The reaction, mixture was stirred for 2 hours, at 25° C., under nitrogen atmosphere. Tributyamine (83 μL, 0.32 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of 6-Dimethyldipropylenetriamine (0.13 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 1 hour at the starting conditions. A solution of Boc-diaminohexane (0.22 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 1 hour at the starting conditions. A solution of Carbodiimidazole (105 mg, 0.65 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. DMF was removed under reduced pressure. Double distilled water (40 mL) was added and the reaction mixture was freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 15 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 5.5, then freeze dried. The remaining solid was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water), then 24 hours at 25° C. (total of 4 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifluoroacetic salt, with a 36% yield. 1H NMR (D2O; 400 MHz): δ 4.32-4.10 (1H, bs), 3.18-1.29 (16H, m).
To a solution of poly-α-glutamic acid (47 mg, 0.36 mmol per monomer) in dry DMF (1 mL) was added a solution of Carbodiimidazole (67 mg, 0.41 mmol) in dry DMF (1 mL). The reaction, mixture was stirred for 1 hour, at 25° C., under nitrogen atmosphere. Tributylamine (87 μL, 0.36 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of Boc-2, 2-iminodiethylamine (0.43 mmol) in dry DMF (1.5 mL) was added and the reaction mixture was stirred for additional 1 hour at the starting conditions. A solution of Carbodiimidazole (124 mg, 0.77 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. DMF was removed under reduced pressure. Double distilled water (40 mL) was added and the reaction mixture was freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 5.5, then freeze dried. The remaining solid was dissolved in double distilled water (20 ml) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water), then 8 hours at 25° C. (total of 2 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifluoroacetic salt, with a 42% yield.
1H NMR (D2O; 400 MHz): δ 4.23 (1H, s), 3.49 (2H, s), 3.33-3.22 (6H, m), 3.1 (1H, s), 2.27 (2H, s), 2.01-1.91 (2H, bs).
To a solution of poly-α-glutamic acid (40 mg, 0.31 mmol per monomer) in dry DMF (1 mL) was added a solution of Carbodiimidazole (67 mg, 0.41 mmol) in dry DMF (1 mL). The reaction, mixture was stirred for 1 hour at 25° C., under nitrogen atmosphere. Tributylamine (74 μL, 0.31 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of Boc-2, 2-iminodiethylamine (0.1 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 1 hour at the starting conditions. A solution of dimethydipropylenetriamine (0.24 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 1 hour at the starting conditions. A solution of Carbodiimidazole (100 mg, 0.62 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. DMF was removed under reduced pressure. Double distilled water (40 ml) was added and the reaction mixture was freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 5.5, then freeze dried. The remaining solid was dissolved in double distilled water (20 ml) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water), then 12 hours at 25° C. (total of 2 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifluoroacetic salt, with a 30% yield. 1H NMR (D2O; 400 MHz): δ 4.12 (1H, s), 3.07-3.74 (15H, m).
To a solution of poly-α-glutamic acid (71 mg, 0.55 mmol per monomer) in dry DMF (2 mL) was added a solution of Carbodiimidazole (101 mg, 0.62 mmol) in dry DMF (1.2 mL). The reaction, mixture was stirred for 1.5 hours at 25° C., under Argon atmosphere. Tributylamine (1.3 mL, 0.55 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of Hexylamine (12.4 mg, 0.12 mmol) and Boc-ethylenediamine (83 mg, 0.52 mmol) in dry DMF (2 mL) was added and the reaction mixture was stirred for additional 3 hours at the starting conditions. A solution of Carbodiimidazole (178 mg, 1.1 mmol) in dry DMF (1.5 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. DMF was removed under reduced pressure. Double distilled water (40 mL) was added and the reaction mixture was freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 7.3 then freeze dried. The left solid was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifluoroacetic salt, with a 44% yield. 1H NMR (D2O; 400 MHz): δ 4.26 (1H, s), 3.42 (1.5H, s), 3.06 (2H, s), 2.33 (2H, s), 1.97 (2H, s), 1.40 (0.5H, s), 1.20 (1.5H, s), 0.78 (0.5H, s).
To a solution of poly-α-glutamic acid (56 mg, 0.43 mmol per monomer) in dry DMF (2.5 mL) was added a solution of Carbodiimidazole (86 mg, 0.53 mmol) in dry DMF (0.7 mL). The reaction, mixture was stirred for 1.5 hours at 25° C., under Argon atmosphere. Tributylamine (1 mL, 0.43 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of Hexylamine (19 mg, 0.19 mmol) and Boc-ethylenediamine (42 mg, 0.26 mmol) in dry DMF (2 mL) was added and the reaction mixture was stirred for additional 2 hours at the starting conditions. A solution of Carbodiimidazole (146 mg, 0.9 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. DMF was removed under reduced pressure. Double distilled water (40 ml) was added and the reaction mixture was freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 5 then freeze dried. The left solid was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifluoroacetic salt, with a 53% yield. 1H NMR (D2O; 400 MHz): δ 4.15 (1H, s), 3.36 (1.5H, s), 3.06 (1H, s), 2.99 (2H, s), 2.26 (2H, bs), 1.90 (2H, bs), 1.33 (1H, s), 1.12 (3H, s), 0.71 (2H, s).
To a solution of poly-α-glutamic acid (50 mg, 0.39 mmol per monomer) in dry DMF (2 mL) was added a solution of Carbodiimidazole (75 mg, 0.46 mmol) in dry DMF (1 mL). The reaction, mixture was stirred for 1.5 hours at 25° C., under Argon atmosphere. Tributylamine (92 μL, 0.39 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of Octylamine (14 mg, 0.11 mmol) and Boc-ethylenediamine (54 mg, 0.34 mmol) in dry DMF (3 mL) was added and the reaction mixture was stirred for additional 2 hours at the starting conditions. A solution of Carbodiimidazole (125 mg, 0.77 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. DMF was removed under reduced pressure. Double distilled water (40 mL) was added and the reaction mixture was freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 6 then freeze dried. The left solid was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifuoroactic salt, with a 52% yield. 1H NMR (D2O; 400 MHz): δ 4.30 (1H, s), 3.46 (1H, s), 3.10 (2H, s), 2.36 (2H, bs), 2.02 (2H, bs), 1.44 (0.5H, s), 1.22 (3H, s), 0.82 (1H, s).
To a solution of poly-α-glutamic acid (42 mg, 0.32 mmol per monomer) in dry DMF (2 mL) was added a solution of Carbodiimidazole (58 mg, 0.45 mmol) in dry DMF (1 mL). The reaction, mixture was stirred for 1.5 hours at 25° C., under Argon atmosphere. Tributylamine (76 μL, 0.32 mmol) was added and the reaction left to stir for 5 more minutes at the same conditions. A solution of Octylamine (20 mg, 0.16 mmol) and Boc-ethylenediamine (34 mg, 0.21 mmol) in dry DMF (3 ml) was added and the reaction mixture was stirred for additional 2 hours at the starting conditions. A solution of Carbodiimidazole (105 mg, 0.65 mmol) in dry DMF (1 ml) was added and the reaction mixture was stirred for additional 12 hours at the starting conditions. DMF was removed under reduced pressure. Double distilled water (40 mL) was added and the reaction mixture was freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes then evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH of 6 then freeze dried. The left solid was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifuoroactic salt, with a 61% yield. 1H NMR (D2O; 400 MHz): δ 4.23 (1H, s), 3.39 (1H, s), 3.03 (1.5H, s), 2.28 (2H, bs), 1.99 (2H, bs), 1.35 (2H, s), 1.13 (5H, s), 0.72 (1.5H, s).
To a solution of poly-α-glutamic acid (40 mg, 0.31 mmol per monomer) in dry DMF (3 mL) was added a solution of Carbodiimidazole (56 mg, 0.35 mmol) in dry DMF (2 mL). The reaction mixture was stirred for 1.5 hours, at 25° C., under Argon atmosphere. Tributylamine (0.1 mL, 0.69 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of Boc-ethylenediamine (32 mg, 0.20 mmol) and butylamine (10 mg, 0.14 mmol) in dry DMF (2.5 mL) was added and the reaction mixture was stirred for additional 3 hours at the starting conditions. A solution of Carbodiimidazole (107 mg, 0.66 mmol) in dry DMF (2 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the left oily residue was dissolved in water (40 mL) and freeze-dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes, and was hereafter evaporated under reduced pressure. The oily residue was dissolved in DD water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to adjust the pH to 5.7, then freeze-dried. The obtained solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of DD water). The aqueous phase was collected and freeze-dried to obtain a white powder as a trifluoroacetic salt, with 49% yield.
1H NMR (D2O; 400 MHz): δ=4.26 (1H, s), 3.44 (1H, s), 2.35 (2H, bs), 1.93 (2H, bs), 1.41 (1H, bs), 1.26 (1H, bs), 0.83 (1.6H, t).
To a solution of poly-α-glutamic acid (47 mg, 0.36 mmol per monomer) in dry DMF (3 mL) was added a solution of Carbodiimidazole (66 mg, 0.41 mmol) in dry DMF (2 mL). The reaction mixture was stirred for 1.5 hours, at 25° C., under Argon atmosphere. Tributylamine (85 μL, 0.36 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of Boc-ethylenediamine (38 mg, 0.24 mmol) and pentylamine (14 mg, 0.16 mmol) in dry DMF (2.5 mL) was added and the reaction mixture was stirred for additional 3 hours at the starting conditions. A solution of Carbodiimidazole (119 mg, 0.72 mmol) in dry DMF (1.5 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the left oily residue was dissolved in water (40 mL) and freeze-dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes, and was thereafter evaporated under reduced pressure. The oily residue was dissolved in DD water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to adjust the pH to 6.5, then freeze-dried. The obtained solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of DD water). The aqueous phase was collected and freeze dried to obtain a white powder as a trifluoroacetic salt, with 39% yield.
1H NMR (D2O; 400 MHz): δ 4.27 (1H, s), 3.45 (1.5H, s), 3.07 (2.5H, s), 2.35 (2H, bs), 1.99 (2H, bs), 1.42 (1.3H, s), 1.23 (2.5H, s), 0.81 (1.75H, bs).
To a solution of poly-α-glutamic acid (47 mg, 0.36 mmol per monomer) in dry DMF (3 mL) was added a solution of Carbodiimidazole (66 mg, 0.41 mmol) in dry DMF (2 mL). The reaction mixture was stirred for 1.5 hours, at 25° C., under Argon atmosphere. Tributylamine (85 μL, 0.36 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of Boc-ethylenediamine (38 mg, 0.24 mmol) and heptylamine (18.4 mg, 0.16 mmol) in dry DMF (2.5 mL) was added and the reaction mixture was stirred for additional 3 hours at the starting conditions. A solution of Carbodiimidazole (119 mg, 0.72 mmol) in dry DMF (1.5 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the left oily residue was dissolved in water (40 mL) and freeze-dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes, and was thereafter evaporated under reduced pressure. The oily residue was dissolved in DD water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to adjust the pH to 6.5, then freeze-dried. The obtained solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of DD water). The aqueous phase was collected and freeze dried to obtain a white powder as a trifluoroacetic salt, with 41% yield.
The molecular weights of Polymers J-P are presented in Table A below.
To a solution of poly-α-glutamic acid (47 mg, 0.36 mmol per monomer) in dry DMF (3 mL) was added a solution of Carbodiimidazole (69 mg, 0.42 mmol) in dry DMF (2 mL). The reaction mixture was stirred for 1.5 hours, at 25° C., under Argon atmosphere. Tributylamine (85 μL, 0.36 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of Boc-ethylenediamine (0.27 mmol), histamine dihydrochloride (0.08 mg) and tributylamine (120 μL) in dry DMF (5 mL) was added and the reaction mixture was stirred for additional 3 hours at the starting conditions. A solution of Carbodiimidazole (120 mg, 0.72 mmol) in dry DMF (2 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the left oily residue was dissolved in water (40 mL) and freeze-dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes and was thereafter evaporated under reduced pressure. The oily residue was dissolved in DD water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to adjust the pH to 5.5, then freeze-dried. The obtained solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of DD water). The aqueous phase was collected and freeze-dried to obtained a white powder as a trifluoroacetic salt, with 30% yield.
1H NMR (D2O; 400 MHz): δ 7.6 (0.25H, S), 6.7 (0.25H, S), 4.16 (1H, s), 3.33 (2H, s), 2.97 (1.5H, s), 2.62 (0.5H, s), 2.22-2.14 (2H, bs), 1.91-1.75 (2H, bs).
To a solution of poly-α-glutamic acid (44 mg, 0.34 mmol per monomer) in dry DMF (3 mL) was added a solution of Carbodiimidazole (62 mg, 0.38 mmol) in dry DMF (2 mL). The reaction mixture was stirred for 1.5 hours, at 25° C., under Argon atmosphere. Tributylamine (81 μL, 0.56 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of histamine dihydrochloride (7 mg, 0.04 mmol), Boc-ethylenediamine (36 mg, 0.22 mmol), hexylamine (12 mg, 0.12 mmol) and tributylamine (64 μL, 0.44 mmol) in dry DMF (3 mL) was added and the reaction mixture was stirred for additional 3 hours at the starting conditions. A solution of Carbodiimidazole (110 mg, 0.68 mmol) in dry DMF (1.5 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze-dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes, and was thereafter evaporated under reduced pressure. The oily residue was dissolved in DD water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to adjust the pH to 6, then freeze-dried. The obtained solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of DD water). The aqueous phase was collected and freeze-dried to obtain a white powder as a trifluoroacetic salt, with 48% yield.
1H NMR (D2O; 400 MHz): δ 7.68 (0.1H, bs), 6.88 (0.1H, bs), 4.26 (1H, bs), 3.44 (1.2H, s), 3.07 (1.7H, s), 2.73 (0.2H, s), 2.35 (2H, bs), 2.05 (2H, bs), 1.40 (0.6H bs), 1.22 (2H, bs), 0.80 (1H, s).
To a solution of poly-α-glutamic acid (42 mg, 0.32 mmol per monomer) in dry DMF (2.5 mL) was added a solution of Carbodiimidazole (64 mg, 0.39 mmol) in dry DMF (1.5 mL). The reaction mixture was stirred for 1.5 hours, at 25° C., under Argon atmosphere. Tributylamine (0.1 mL, 0.69 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of hexyamine (11 mg, 0.11 mmol), Boc-ethylenediamine (22 mg, 0.14 mmol), histamine dihydrochloride (19 mg, 0.12 mmol) and tributylamine (100 μL, 0.69 mmol) in dry DMF (3.5 mL) was added and the reaction mixture was stirred for additional 3 hours at the starting conditions. A solution of Carbodiimidazole (109 mg, 0.67 mmol) in dry DMF (1.5 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze-dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes, and was thereafter evaporated under reduced pressure. The oily residue was dissolved in DD water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to adjust the pH to 6.3, then freeze-dried. The left solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of DD water). The aqueous phase was collected and freeze-dried to afford a white powder as a trifluoroacetic salt, with 43% yield.
1H NMR (D2O; 400 MHz): δ 7.73 (0.25H, bs), 6.90 (0.25H, bs), 4.23 (1H, bs), 3.44-3.37 (1.3H, bs), 3.08 (1.3H, s), 2.72 (0.6H, s), 2.34-2.29 (2H, bs), 2.05 (2H, bs), 1.38 (0.5H bs), 1.19 (2H, bs), 0.79 (1H, s).
To a solution of poly-α-glutamic acid (34 mg, 0.26 mmol per monomer) in dry DMF (2.5 mL) was added a solution of Carbodiimidazole (47 mg, 0.28 mmol) in dry DMF (1.5 mL). The reaction mixture was stirred for 2 hours, at 25° C., under Argon atmosphere. Tributylamine (0.1 mL, 0.69 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of undecylamine (14 mg, 0.08 mmol) and tributylamine (32 μL, 0.22 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 3 hours at the starting conditions. A solution of Boc-ethylenediamine (33 mg, 0.21 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 2 hours. A solution of Carbodiimidazole (85 mg, 0.52 mmol) in dry DMF (1 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze-dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes, and was thereafter evaporated under reduced pressure. The oily residue was dissolved in DD water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to adjust the pH to 6, then freeze-dried. The obtained solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of DD water). The aqueous phase was collected and freeze-dried to afford a white powder as a trifluoroacetic salt, with 42% yield.
1H NMR (D2O; 400 MHz): δ 4.28 (1H, bs), 3.70 (0.15H, s), 3.45 (1.5H, s), 3.09 (1.5H, s), 2.35 (2H, bs), 2.06 (2H, bs), 1.21 (2.6H, bs), 0.81 (1.2H, s).
To a solution of poly-α-glutamic acid (32 mg, 0.25 mmol per monomer) in dry DMF (2.5 mL) was added a solution of Carbodiimidazole (45 mg, 0.27 mmol) in dry DMF (1.5 mL). The reaction mixture was stirred for 2 hours, at 25° C., under Argon atmosphere. Tributylamine (0.1 mL, 0.69 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of undecylamine (27 mg, 0.15 mmol) and tributylamine (64 μL, 0.44 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 2 hours at the starting conditions. A solution of Boc-ethylenediamine (32 mg, 0.21 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 2 hours. A solution of Carbodiimidazole (81 mg, 0.5 mmol) in dry DMF (1 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze-dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes, and was thereafter evaporated under reduced pressure. The oily residue was dissolved in DD water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to adjust the pH to 6.8, then freeze-dried. The obtained solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of DD water). The aqueous phase was collected and freeze-dried to afford a white powder as a trifluoroacetic salt, with 37% yield.
1H NMR (D2O; 400 MHz): δ 4.27-4.25 (1H, bs), 3.72 (0.2H, s), 3.45 (1.2H, s), 3.08 (1.2H, s), 2.35-1.94 (4H, bs), 1.20 (6H, bs), 0.80 (2.5H, s).
To a solution of poly-α-glutamic acid (33 mg, 0.26 mmol per monomer) in dry DMF (2.5 mL) was added a solution of Carbodiimidazole (46 mg, 0.28 mmol) in dry DMF (1.5 mL). The reaction mixture was stirred for 2 hours, at 25° C., under Argon atmosphere. Tributylamine (0.1 mL, 0.69 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of 1-propylbutylamine (10 mg, 0.09 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 3 hours at the starting conditions. A solution of Boc-ethylenediamine (26 mg, 0.16 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 2 hours. A solution of Carbodiimidazole (84 mg, 0.52 mmol) in dry DMF (1 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze-dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes, and was thereafter evaporated under reduced pressure. The oily residue was dissolved in DD water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to adjust the pH to 6.3, then freeze-dried. The obtained solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 liter of DD water). The aqueous phase was collected and freeze-dried to afford a white powder as a trifluoroacetic salt, with 37% yield.
1H NMR (D2O; 400 MHz): δ 4.26 (1H, bs), 3.74 (0.3H, s) 3.45 (1H, s), 3.08 (1H, s), 2.35 (2H, bs), 2.07 (2H, bs), 1.41-1.24 (4H, s), 0.81 (3H, t).
To a solution of poly-γ-glutamic acid (180 mg, 1.39 mmol per monomer) in dry DMF (12 mL) was added a solution of Carbodiimidazole (259 mg, 1.60 mmol) in dry DMF (3 mL). The reaction mixture was stirred for 2 hours, at 25° C., under Argon atmosphere. Tributylamine (0.4 mL, 2.76 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of dimethyldipropylenetriamine (135 mg, 0.85 mmol) and hexylamine (60 mg, 0.59 mmol) in dry DMF (2 mL) was added and the reaction mixture was stirred for additional 4 hours at the starting conditions. A solution of Carbodiimidazole (452 mg, 2.79 mmol) in dry DMF (3 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze-dried. The residue was dissolved in DD water (40 mL) and the mixture was treated with a 10% HCl to adjust the pH to 4.5. The aqueous phase was then extracted with DCM (40 mL) and Diethylether (40 mL). The aqueous phase was then collected and treated with 10% NaOH solution to adjust the pH to 6.5 and then freeze-dried. The obtained solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of DD water) and at 25° C. for additional 12 hours. The aqueous phase was collected and freeze-dried to afford a white powder as a chloride salt, with 40% yield.
1H NMR (D2O; 400 MHz): δ 4.25 (1H, bs), 3.20-3.11 (2H, bs), 2.82 (2H, bs), 2.53 (2H, bs), 2.31 (1H, bs), 1.87-1.76 (3H, bs), 1.42 (0.5H, s), 1.22 (2H, s), 0.81 (1H, s).
To a solution of poly-γ-glutamic acid (105 mg, 0.81 mmol per monomer) in dry DMF (7 mL) was added a solution of Carbodiimidazole (149 mg, 0.92 mmol) in dry DMF (3 mL). The reaction mixture was stirred for 2 hours, at 25° C., under Argon atmosphere. Tributylamine (0.2 mL, 1.38 mmol) was added and the reaction left to stir for 10 more minutes at the same conditions. A solution of dimethyldipropylenetriamine (52 mg, 0.33 mmol), Boc-ethylenediamine (28 mg, 0.18 mmol) and hexylamine (34 mg, 0.34 mmol) in dry DMF (7 mL) was added and the reaction mixture was stirred for additional 4 hours at the starting conditions. A solution of Carbodiimidazole (262 mg, 1.62 mmol) in dry DMF (3 mL) was added and the reaction mixture was left at the starting conditions for additional 12 hours. DMF was removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze-dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes, and was thereafter evaporated under reduced pressure. The oily residue was dissolved in DD water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to adjust the pH to 6, then freeze-dried. The obtained solid was dissolved in DD water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 L of DD water) and then for 12 hours at 25° C. The aqueous phase was collected and freeze-dried to afford a white powder as a trifluoroacetic salt, with 18% yield.
1H NMR (D2O; 400 MHz): δ 4.26 (1H, bs), 3.3-2.82 (6H, bm), 2.32-1.82 (4H, bm), 1.42 (0.5H, s), 1.22 (3H, s), 0.81 (1.5H, s).
Crosslinked PGAamine polymers are synthesized from a co-polymer of L-PGA and backbone units featuring a cross-linkable group (e.g., lysine backbone units), using a suitable cross-linking agent to cross link the cross-linkable moieties. Then a coupling reagent is used to conjugate amination moieties to the pending carboxylic groups of the glutamic acid units, as exemplified in
A solution of co-polymer-lysine(10%)-L-polyglutamate(90%) (98 mg) in DDW (3 mL) was treated with a solution of 10% NaOH to reach a clear solution (pH=12), then a solution of 5% glutaraaldehye (6.5 μL) in DDW was added and the reaction mixture was stirred for 12 hours, at 25° C. DDW (20 mL) was added and the reaction mixture was treated with 10% TFA solution in DDW to pH=7 and then freeze dried. The remaining solid was dissolved in double distilled water (20 mL) and dialyzed for 72 hours at 4° C. (total of 8 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder. The solid was dissolved in DDW (3 mL) and treated with 10% HCl solution to pH=1. The mixture was kept for 1 hour at 25° C. The solid was isolated by centrifugation (4500 rpm, 5 minutes at 4° C.), washed with DDW and then freeze dried to afford a white powder at a 43% yield.
The polymer was analyzed by static light scattering technique, using agilent 1200 series HPLC system (Agilent Technologies) equipped with a multi angle light scattering detector (Dawn Heleos, Wyatt) and Shodex Kw404-4F column (Showa Denko America, Inc.). Molecular weight and PDIs derived from the analysis indicate 2.97×104 grams/mol and around 1.2, respectively.
A solution of cross linked co-polymer-lysine(10%)-L-polyglutamate(90%) (35 mg) in dry DMF (3 ml) was added to a solution of Carbodiimidazole (63 mg) in dry DMF (2 ml). The reaction mixture was stirred for 2 hours, at 25° C., under Argon atmosphere. Tributylamine (94 μl, 0.39 mmol) was added and the reaction was left to stir for 5 more minutes at the same conditions. A solution of Boc-Ethylenediamine (66 mg) in dry DMF (1.2 mL) was added and the reaction mixture was stirred for additional 3 hours at the starting conditions. A solution of Carbodiimidazole (92 mg) in dry DMF (1 mL) was added and the reaction mixture was stirred at 25° C., under Argon for additional 12 hours. DMF was removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (5 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes and thereafter evaporated under reduced pressure. The reaction mixture was treated with a 10% NaOH solution to reach pH=7.0, then freeze dried. The remaining solid was dissolved in double distilled water (20 mL) and dialyzed for 48 hours at 4° C. (total of 8 liters of double distilled water). The aqueous phase was collected and freeze dried to afford a white powder as a trifluoraoacetic salt, at a 73% yield. 1H NMR (D2O; 400 MHz): δ 4.17 (1H, s), 3.32 (2H, s), 2.95 (2H, s), 2.22 (2H, s), 1.91-1.80 (2H, bs).
Block co-polymer are synthesized by preparing a block copolymer of L-polyglutamate and an amino acid derivative featuring an alkyl pendant group. A CDI coupling agent was thereafter used to conjugate amination moieties on the pending carboxylic groups of the glutamic acid units, as exemplified in
To a solution of 4-Oxazolidinepropanoic acid, 2,5-dioxo-, phenylmethyl ester (507 mg, 1.88 mmol) in dry DCM (20 mL) was added hexylamine (1.2 μL) and the reaction mixture was stirred for 8 days, at 12° C., under Argon. A solution of 4-hexyl-2,5-Oxazolidinedione (232 mg, 1.25 mmol) in dry DCM (15 mL) was added and the reaction mixture was stirred for 3 more days, at 12° C., under Argon atmosphere, then decanted to a cold diethyl ether (200 mL) and kept at −12° C. for 12 hours. The obtained solid was isolated by centrifugation (4500 rpm, 5 minutes, 4° C.) and dried under reduced pressure. The residual solid was dissolved in TFA (6 mL), a solution of 33% HBr in AcOH (6 mL) was added and the reaction mixture was stirred for 1 hour at 25° C. The reaction mixture was thereafter decanted to cold diethyl ether (80 mL) and kept at −12° C. for 12 hours. The solid was isolated by centrifugation and dried under reduced pressure to afford the intermediate copolymer at a yield of 48%.
To a solution of co-polymer-D,L-α-hexyl-amino acid-L-polyglutamate (29 mg, 0.11 mmol) in dry DMF (6 mL) was added a solution of Carbodiimidazole (42 mg, 0.26 mmol) in dry DMF (1 ml). The reaction, mixture was stirred for 2 hours, at 25° C., under Argon atmosphere. Tributylamine (0.1 mL, 0.4 mmol) was added and the reaction was left to stir for 5 more minutes at the same conditions. A solution of Boc-Ethylenediamine (54 mg, 0.34 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred for additional 4 hours at the starting conditions. A solution of Carbodiimidazole (74 mg, 0.46 mmol) in dry DMF (1 mL) was added and the reaction mixture was stirred at 25° C., under Argon for additional 12 hours. DMF was then removed under reduced pressure and the remaining oily residue was dissolved in water (40 mL) and freeze dried. The resulting solid was dissolved in DCM (5 mL) and Trifluoroacetic acid (7 mL) was added at 0° C. The mixture was stirred at 25° C. for 10 minutes and thereafter evaporated under reduced pressure. The oily residue was dissolved in double distilled water (40 mL) and the aqueous phase was extracted with DCM (2×50 mL) and diethyl ether (50 mL). The aqueous phase was collected and treated with a 10% NaOH solution to reach pH=5, then freeze dried. The remaining solid was dissolved in double distilled water (20 mL) and dialyzed for 72 hours at 4° C. (total of 8 L of double distilled water). The aqueous phase was collected and freeze dried to receive a white powder as a trifluoraoacetic salt.
1H NMR (D20; 400 MHz): δ 4.17 (1H, s), 3.32 (1.6, s), 2.95 (1.8H, s), 2.23 (2H, s), 1.92, (2H, bs), 1.1 (0.7H, bs), 0.6 (0.6H, bs).
1H-NMR Characterization of the Amination Products:
The various products of the amination synthesis illustrated in
Characterization of the PGA Precursor Used for PGAamine Polymers A-I Synthesis:
The precursor PGA polymers were analyzed by static light scattering technique, using agilent 1200 series HPLC system (Agilent Technologies) equipped with a multi angle light scattering detector (Dawn Heleos, Wyatt) and Shodex Kw404-4F column (Showa Denko America, Inc.) molecular weight and PDIs were derived from the analysis, and have ranged between 6300 to 8500 g/mol and around 1.2 respectively. The number of monomers per polymer was calculated according to the molecular weight obtained by SLS measurement.
Table 1 below presents the Molecular weight, polydispersity index and calculated number of monomers of the PGA precursor used for PGAamine polymer synthesis as analyzed by SLS (Table 1 presents a characterization of an exemplary PGA precursor used in the synthesis of PGAamine polymers A-I, according to some embodiments of the present invention).
Characterization of the Electrostatic Interaction Between PGAamine Amination Derivatives and siRNA:
Complex formation of PGAamines A-I with siRNA was investigated by gel electrophoresis mobility shift assay (EMSA) (
Both polymers A and B have shown complete complexation starting from 2 N/P ratio. Polymer C has also complexed with siRNA at 2 N/P ratio, indicating that branching of the terminal amine did not affect the minimal complexation ratio.
The Strength of the complexation of polyplex C (tertiary terminal amine) was higher than that of polyplex A (primary terminal amine), as indicated by the higher amount of the anion heparin required in order to displace the siRNA from its binding to the polymer (0.075 IU heparin/50 pmol siRNA compared with only 0.025 IU required in polyplex A. This stronger complexation was also approved by the decreased intensity of the ethidium bromide fluorescence at 10 N/P ratio shown in the EMSA of polyplex C. This phenomena results from exclusion of ethidium bromide for its intercalation sites with siRNA by the strong affinity of the oligonucleotides to the polymer [A. J. Geall, I. S. Blagbrough, Journal of pharmaceutical and biomedical analysis 22, 849-859 (2000); published online EpubJun]. The combination of two different side chains on one polymer: one ends with tertiary amine and the other with primary amine seems to result in lower affinity towards siRNA and higher minimal complexation ratio, as indicated for Polymers D and E. Polymer E with the longer side chains had slightly better complexation qualities exhibiting 3 N/P ratio minimal complexation ratio compared to 5 N/P minimal complexation ratio obtained by polymer D. Adding a secondary amine to moieties ending by tertiary amine have restored the complexation qualities, as shown by complexation properties of polymers F and G that exhibited minimal complexation ratios of 1 and 2 N/P respectively. The addition of a secondary amine, aimed to increase buffering capabilities, strengthened the complexation with siRNA, as demonstrated by heparin displacement assay performed on polymer F indicating that the siRNA was not displaced even in the presence of 0.25 IU heparin (
The EMSA image shows that minimal neutralization of charge was obtained only at 10 N/P ratio. This relatively low surface charge of polyplex H at 5 N/P ratio was further approved by zeta potential analysis (see, Table 2 below). Complexation qualities were restored again when the latter side-chain moiety was combined with additional moiety that bears tertiary terminal amine and secondary amine, as indicated by Polymer I. This structure resulted in minimal complexation ratio of 1 N/P, indicating strong attraction between PGAamine polymer to siRNA.
Size and Charge Characterization of PGAamine:Rac1 siRNA Polyplexes:
Zeta potential analysis of the various PGAamine:siRNA polyplexes was performed in order to assess the surface charges of the polyplexes.
Zeta potentials and hydrodynamic radiuses were obtained by Zetasizer ZS at 633 nm wavelength and by NS300 at 532 nm respectively. SEM images were obtained by Quanta 200 FEG Environmental SEM.
Table 2 below presents the Zeta potential, hydrodynamic diameter values and Diameter as imaged by SEM of PGAamine:siRNA polyplexes at selected N/P ratios.
Zeta potentials of the 5 N/P ratio polyplexes A, C, D, E, F, G, H and I and of 10 N/P ratio polyplex B have ranged between 0 to 25 mV. Polyplexes A and B, that bear side chain moieties with primary terminal amine, had relatively high zeta potentials of 25.4±4.85 and 17.5±7.42 mV, respectively. The transition to tertiary terminal amine resulted in reduced zeta potential as indicated by the charge of polyplex C (3.71±6.47 mV). Combining both tertiary and primary terminal amine side chains on one backbone did not restore the high zeta potential, as indicated by charges of polyplexes D and E (0.914±3.39 and 6.8±2.96 mV, respectively). Vast addition of secondary amines to the tertiary amine-bearing moieties has resulted in increased surface charge (polyplex F with 15.3±4.42 mV). Polyplex G with the low percentage of secondary amines had lower surface charge (4.13±3.47 mV), while the addition of a secondary amine to a terminal primary amine backbone resulted in almost neutral zeta potential (H, 0.415±3.55 mV). Polyplex I with high percentage of tertiary terminal amines and secondary amines had also high positive charge of 18.9±4.62 mV.
The zeta potential of higher N/P ratio polyplexes was further tested and the data is summarized in Table 4 below. The increase in N/P ratio generally resulted in increased zeta potential.
The size and morphology of the polyplexes were evaluated using DLS and SEM (see, Table 2 above and
Particles at this size range are assumed to selectively accumulate in the tumor tissue due to the enhanced permeability and retention (EPR) effect [Scomparin et al, Biotechnology advances, 33, 1294-1309 (2015); published online EpubApr 25 (10.1016/j.biotechadv.2015.04.008].
Higher N/P ratio polyplexes were measured for their hydrodynamic diameter using Vasco DLS, and the obtained data is presented in Table 3 below. Polyplexes have either increased their size or remained at nearly similar size with the increase in N/P ratio.
Table 4 below presented the Zeta potential values of high N/P ratio polyplexes as obtained by zetasizer ZS.
15 ± 4.11
Membrane Crossing and Intracellular Trafficking of PGAamine:siRNA Polyplexes:
One of the major obstacles in the therapeutic usage of siRNA is their poor cellular penetration [A. Scomparin, D. Polyak, A. Krivitsky, R. Satchi-Fainaro, Biotechnology advances, 33, 1294-1309 (2015); published online EpubApr 25 (10.1016/j.biotechadv.2015.04.008]. The ability of PGAamine polymers to assist membrane-crossing of siRNA was evaluated using confocal microscopy and the obtained data is presented in
Polyplexes A, B, F and I were further tested for their intracellular trafficking, and the obtained data is presented in
In previous works in which the internalization mechanisms and intracellular trafficking of cationic polymers were studied, both Macropinocytosis, Clathrin-mediated endocytosis (CME) and Caveole-mediated endocytosis (CvME) were indicated as possible parallel routes for cellular internalization of polyplexes [Hess et al., Biochimica et biophysica acta 1773, 1583-1588 (2007); Xiang ET AL., Journal of controlled release: official journal of the Controlled Release Society 158, 371-378 (2012)].
To distinguish the CME from the other pathways, ammonium chloride, a cytosolic acidification agent was used [Xiang et al., 2012 (supra); Ofek et al., FASEB journal: official publication of the Federation of American Societies for Experimental Biology 24, 3122-3134 (2010)].
Colocalization with late lysosomes was further evaluated using the specific marker LAMP-1 [Xiang et al., 2012 (supra)], as shown in
Although all 3 possible pathways (macropinocytosis, CME and CvME) fuse with the lysosome, the silencing activity of cationic polyplexes is traditionally attributed to their ability to escape the endosome and locate at the cytoplasm by an endosomal buffering mechanism formally termed “the proton sponge effect” [Boussif et al., Proceedings of the National Academy of Sciences of the United States of America 92, 7297-7301 (1995)].
Regardless of the escape mechanism, the cytoplasm is the site of activity for the siRNA, and at least some portion of it should locate there in order to efficiently silence gene's expression.
Silencing Activity of PGAamine:Rac1 siRNA Polyplexes:
To further evaluate the silencing potential of the PGAamine polymers as delivery vehicles of siRNA, dual luciferase reporter assay was implied (see,
To better evaluate the performance of the polyplexes, linear PEI and lipofectamine as positive control nanocarriers for transfection were used. HeLa and SKOV-3 cells were treated with 50 nM of the commercial transfection reagents jetPRIME and lipofectamine (marked PEI and lipo respectively in
The studies herein focused on N/P ratios of either 5 or 10, since these are the most applicable ratios for the polymer based delivery system. As, in some embodiments, about 100% of the functional pendent groups of the PGA are modified, each added amine unit means an additional monomer. Higher N/P ratios, therefore, result in large amounts of polymer administered only as a delivery vehicle.
The silencing activity of polymers that were not active at 5 or 10 N/P ratios at increasing ratios up to 100 N/P was tested. The increase was limited to the point of indicated toxicity, that is, viability reduction to less than 0.75-fold (see,
While evaluating the activity of the polyplexes on SKOV-3 cells, it was found that polyplexes C and G exhibited silencing activity at 15 N/P ratio, while E polyplex was active at the higher 25 N/P ratio. Except for polyplex G evaluated on SKOV-3 cell line, all other polyplexes that were active at the high N/P ratios (15 N/P and more) were also toxic at the relevant concentrations.
To further evaluate the biological silencing activity of polyplexes A-I, a transwell migration assay on SKOV-3 cells was performed using 20% FBS-containing serum as incentive for migration and Rac1 siRNA as migration inhibitor. Rac1 is a member of the Rho small GTPase proteins family and its role in cell motility in embryonic development and tumor invasiveness is well established. Recently, its role in epithelial-mesenchymal transition (EMT) towards migration and metastasis of cancer cells was demonstrated, placing Rac1 as an attractive anti-cancer target.
Inhibition of migration obtained following 48 hours of treatment with A, B, F and I polyplexes composed of PGAamine and Rac1 siRNA, while polyplexes containing eGFP control siRNA were unable to inhibit cell migration.
Inhibition of serum-induced migration of SKOV-3 cells is the result of downregulation of Rac1 mRNA induced by our PGAamine:Rac1 siRNA A, B, F and I polyplexes. These results support the data obtained in the Dual luciferase assay and confocal cellular internalization analysis: polymers A, B, F and I had the ability to assist siRNA cellular internalization, and to downregulate gene's expression.
Inhibition of Cellular Motility by PGAamine A:Rac1 siRNA Polyplexes:
The ability of PGAamine A:siRac1 polyplex to inhibit cells' motility by Rac1 knockdown was evaluated in thin-layer wound healing assay. IncuCyte ZOOM® live cell imaging showed that PGAamine A:siRac1 polyplex inhibited the migration of SKOV-3 cells by 35% as opposed to control treatments, as presented in
Plasma Stability and Immune- and Hemo-Compatibility in Ex Vivo Blood Compartment:
The ability of the siRNA-polymer complex to stay intact in the blood was evaluated by incubating PGAamine A:siRac1 polyplex in 100% mouse plasma for up to 24 hours. Plasma-polyplex mixtures were then loaded on 2% agarose gel and electrophoresis was performed to assess the amount of siRNA released from the polyplex. No release of siRNA was seen following incubation of the polyplex in plasma as implied by the absence of free-siRNA running towards the cathode (see,
The interactions of PGAamine:siRNA polyplex with blood compartment were tested using a series of ex vivo assays.
Hematocompatibility of PGAamine A:siRac1 polyplex was assessed by measuring red blood cells (RBC) lysis. The concentrations of PGAamine:siRac1 polyplex used were the relevant in vivo concentrations, adjusted to dilution in the mouse blood volume (0.417 mg/mL polymer is equivalent to 8 mg/kg siRNA for 25 g mouse with 2 mL blood volume). The results are depicted in
Measurement of PGAamine A:Rac1 siRNA Polyplex-Mediated Immune Response:
Complement activation following treatment with PGAamine A:Rac1 siRNA 5 N/P ratio polyplex was evaluated by quantification of the complement terminal complex SC5b-9 present in human plasma, and the results are presented in
Furthermore, the effect of a polymer alone or in complex with siRNA on cytokines secretion and interferon responsive genes on normal human peripheral blood mononuclear cells (PBMCs) was evaluated and the results are presented in
The effect of PGAamine A:Rac1 siRNA polyplex on inflammatory genes expression was also assessed (
In Vivo Toxicity of PGAamine:Rac1 siRNA Polyplexes
Maximum tolerated dose (MTD) of A, B, F and I polyplexes was performed by evaluating the viability of BALB/c mice following single IV (intravenous) injection.
Table 5 below presents the maximum tolerated dose of polyplexes A, B, F and I at N/P ratios of 5 (polymers A, F and I) or 10 (polymer B) for in vivo treatments injected i.v. to BALB/c mice at 400 μL/mouse dose. The MTD of polyplex A was the highest—above 8 mg/kg, polyplexes F and B were tolerated at above 6 mg/kg and polyplex I exhibited MTD of 1 mg/kg.
Activity of PGAamine:siRNA Polyplex Evaluated Following IP or IV Administration in Human and Murine In Vivo Models:
The accumulation of PGAamineA:Rac1 siRNA polyplexes at N/P 5 in tumor tissue was assessed after 3 sequential intraperitoneal (IP) injections (about 24 hours interval), in the orthotopic Skov-3 human ovarian carcinoma model in athymic nude female mice. Followed by collection of tumors 24 hours post the 3rd injection and analyzes for accumulation of Rac1 siRNA. The results indicate 8-fold and 2.75-fold increase in Rac1 siRNA tumor accumulation following treatment with A:Rac1 siRNA polyplexes compared to treatment with saline or siRNA alone, respectively (see,
Furthermore, C57 mice bearing subcutaneous LLC tumors were treated via the tail vein (IV) with PGAamineA:Rac1 siRNA polyplexes at N/P 5 as described above. The analyzes of collected tumor tissues showed Rac1 gene knockdown of 47% in PGAamineA:Rac1 siRNA polyplexes treated mice compared to saline treated mice (see,
Anti-Cancer Efficacy of PGAamine:Plk1 siRNA Polyplexes in Skov-3 mCherry-Labeled Orthotopic Tumor Bearing Nu/Nu Mice:
The potential of PGAamine-based polyplex to inhibit tumor growth of ovarian carcinoma was tested. The Plk1 gene was selected as a target with the PGAamine:siPlk polyplex. Deregulation of Plk1 was shown to be responsible for mitotic defects, by affecting cell cycle checkpoints, thus resulting in aneuploidy and tumorigenesis. Overexpression of Plk1 was observed in many cancerous tissues, including ovarian carcinoma and was shown to correlate with tumor stage, grade and poor patient prognosis. Since Plk1 is considered as a “proto-oncogene”, inhibition of Plk1 is effective treatment for cancers.
In vivo anticancer efficacy of Plk1 siRNA complexed with A PGAamine was evaluated in nu/nu mice bearing orthotopic intraperitoneal tumors of mCherry-labeled SKOV-3 human ovarian adenocarcinoma cells. Following 9 every other day intraperitoneal injections of PGAamine:siRNA polyplexes (8 mg/kg siRNA) (as shown in
Characterization of the Electrostatic Interaction Between Alkylated PGAamine Derivatives and siRNA:
For each of polymers J-M, complex formation with siRNA was investigated by gel electrophoresis mobility shift assay (EMSA), and the obtained data is presented in
Polymer J fully complexed with siRNA from 2 N/P ratio and on as indicated by reversing the migration of siRNA towards the negative electrode. Polymer K was forming polyplexes from 1.5 N/P ratio and on, as indicated by the partial inhibition of migration compared to free siRNA. Zeta potential measurements of K:siRNA in 1.5 N/P ratio showed slightly negative charge of the complex (−2.56±3.79 mV), that further resulted in partial migration towards the positively charged electrode. The reduction in ethidium bromide fluorescence at the higher ratios indicates the strong affinity between siRNA and the polymer resulting in exclusion of ethidium bromide from its attachment to the siRNA. Similar phenomenon is illustrated in polymers L and M, when fluorescence of ethidium bromide is decreased with the increase of N/P ratio. Lowest full complexation ratios of polymers L and M with siRNA are 1 and 2, respectively.
Both polymers N and O are fully complexed with siRNA at N/P ratio 2 and above as indicated by reversed migration of siRNA towards the anode. Polymer P fully complexed with siRNA from 3 N/P ratio, reduction in the band's strength in 5, 8 and 10 N/P might indicate strong affinity between polymer and siRNA and the resulting ethidium-bromide exclusion.
Silencing Activity of Alkylated PGAamine:Rac1 siRNA Polyplexes:
Evaluation of the silencing activity of polymers J-P when forming polyplexes with siRNA was done by Dual luciferase assay as described hereinabove and the results are presented in
Polyplex O at 2 N/P ratio and 100 and 250 nM concentrations, 3 N/P ratio at 100 nM concentration and 5 N/P ratio at 100, 250 and 500 nM concentrations have also demonstrated higher than 80% silencing activity, mostly with retained more than 80% viability, toxic N/P ratios and concentrations that have demonstrated 25%-35% percent reduction in viability were 3 N/P ratio at 250 nM concentration and 5 N/P ratio at 100 and 250 nM concentration.
K:siRNA, M:siRNA and O:siRNA polyplexes have shown interesting phenomenon of decreased silencing efficiency with increasing N/P ratios and treatment concentrations, that might be explained by alterations in supramolecular rearrangement.
Polyplex P have demonstrated moderate (more than 50%) silencing activity at 3 N/P ratio and concentration of 250 and 500 nM siRNA and at 5 N/P ratio at concentrations 100 and 250 nM siRNA and high silencing activity (more than 80%) at 2 N/P and concentrations 100, 250 and 500 nM, 3 N/P ratio and concentration of 100 nM siRNA and 5 N/P and 500 nM siRNA concentration.
Polyplex N:siRNA at 2, 3 or 5 N/P ratio have shown no silencing activity, due to its short 4 carbon alkyl moiety, demonstrating the lower limit required (side chain of 5 carbons) for the length of the alkyl-side chain of the PGAamine polyplexes constructed of polymers bearing 40% alkyl-moiety and 60% ethylene-diamine moiety in order to have in-vitro silencing activity by dual-luciferase assay.
These data indicate that the optimal percentage of the alkyl-moiety in terms of silencing activity is around 40%, as demonstrated by improved silencing activity of polyplexes K, O, P and M comparing to J and L (20% alkyl). For the length of the alkyl moiety, it is demonstrated that the alkyl chain should have more than 4 carbons, as shown by lack of silencing activity demonstrated by polyplex N compared to good silencing activity demonstrated by polyplexes K, O and P (6, 5 and 7 carbons respectively). Good silencing activity was demonstrated also by polyplexes containing PGAamine polymers bearing 8 and 9 carbon chains as an alkyl moiety (data not shown).
In Vivo Toxicity of Alkylated PGAamine K:Rac1 siRNA Polyplexes at 2 N/P Ratios:
To determine the in vivo toxicity of K:Rac1 siRNA polyplexes at 2 N/P ratios, the viability of BALB/c mice following single i.v. injection at 200 μL/mouse dosage of alkylated PGAamine K polymer complexed with Rac1 siRNA was tested. The mice were viable following 8 and 15 mg/kg siRNA dosage. Data is presented in Table 6.
Characterization of the Electrostatic Interaction Between Imidazole-Bearing PGAamine Derivatives and siRNA:
For each of polymers Q-T, complex formation with siRNA was investigated by gel electrophoresis mobility shift assay (EMSA), and the obtained data is presented in
Silencing Activity of Imidazolated PGAamine:Rac1 siRNA Polyplexes:
Evaluation of the silencing activity of polymers Q-T when forming polyplexes with siRNA was done by Dual luciferase assay as described hereinabove and the results are presented in
Altogether when determining the desired properties of imidazolated PGAamine polymers as a delivery vehicle to siRNA, based on silencing activity properties, it is indicated that polymers containing imidazole ring and ethylenediamine moiety exclusively are inactive, while the addition of an alkyl moiety restore the silencing activity, only in case that the imidazole moiety rate exceeding 10% (in this case 30% of imidazole ring along with 40% ethylenediamine and 30% of alkyl moiety).
Branched Alkyl-Bearing PGAamine Polymers and siRNA Polyplexes Therewith
Characterization of the Electrostatic Interaction Between Branched Alkyl-Bearing PGAamine Derivatives and siRNA:
For each of polymers U-W, complex formation with siRNA was investigated by gel electrophoresis mobility shift assay (EMSA), and the obtained data is presented in
Silencing Activity of Dialkylated PGAamine:Rac1 siRNA Polyplexes:
Evaluation of the silencing activity of polymers U-W when forming polyplexes with siRNA was done by Dual luciferase assay as described hereinabove and the results are presented in
Characterization of the Electrostatic Interaction Between X and Y PGAamine Derivatives and siRNA:
For each of polymers X and Y, complex formation with siRNA was investigated by gel electrophoresis mobility shift assay (EMSA), and the obtained data is presented in
Silencing Activity of X and Y PGAamine:siRNA Polyplexes:
Evaluation of the silencing activity of polymers X and Y when forming polyplexes with siRNA was done by Dual luciferase assay as described hereinabove and the results are presented in
Complex formation between Polymer CL1, as described herein, and siRNA was investigated by gel electrophoresis mobility shift assay (EMSA), and the obtained data is presented in
Silencing Activity of CL1:siRNA Polyplexes:
Evaluation of the silencing activity of Polymer CL1 when forming polyplex with siRNA was done by Dual luciferase assay as described hereinabove and the results are presented in
Complex formation between Co-polymer BL1 and siRNA was investigated by gel electrophoresis mobility shift assay (EMSA), and the obtained data is presented in
Formulation of PGAamineA:siRNA Polyplex:
Following physicochemical characterization of Polymer A:siRNA polyplexes in low concentrations and pure water, Malvern zetasizer ZS DLS measurements have revealed problematic physicochemical profile. The polyplexes had high tendency to aggregate forming microparticles with diameter of 5218±633.3 nm and very high polydispersity (PDI=1.0) (
A formulation of Polymer A:siRNA polyplex was therefore designed in order to maintain stable and discrete nanoparticles. It was uncovered that the addition of 0.2%-10% (molar ratio with the polymer) Tween®20 assisted in maintaining discrete polymer particles in aqueous solution. Polyplexes constructed from polymers that were first dissolved in 0.2 and 2% Tween® solution (molar ratio) and siRNA at 5 N/P ratio have demonstrated size homogeneity and narrower dispersity (PDI=0.323) as analyzed by Malvern zetasizer ZS and imaged in
In view of these results, the N/P ratio of the polyplexes was decreased in order to optimize structural features of the polyplexes. Polyplexes dissolved first in 0.2% Tween® and then complexed with siRNA at 2 N/P ratio have demonstrated micellar-like structure with hydrodynamic radius of 173.3±60.51 nm and narrow polydispersity (PDI=0.213), as analyzed by Malvern zetasizer ZS and presented in
Thus, it has been demonstrated that the addition of 0.2-10% surfactant to PGAamines not bearing an alkyl-moiety assists in forming ordered discrete and around 100 nm diameter sized polyplexes when assembled manually at 2 N/P ratio with oligonucleotides.
Formulation of Polymer K:siRNA Polyplex
Physicochemical characteristics of Polymer K:siRNA polyplexes have suffered from strong aggregation tendency and heterogeneity as described above regarding Polymer A:siRNA polyplexes. DLS measurements have revealed size of 2786±454.9 nm and high polydispersity of 1.0 (
In order to improve these characteristics a formulation of Polymer K:siRNA polyplexes was designed. For improved distribution, controlled assembly was used via a microfluidic system. This system introduces the two solutions (polymer solution and siRNA solution) on a very thin interface, to thereby prevent aggregates that stem from high local concentrations of polymer or siRNA during bulk interaction when the two solutions are mixed manually. Both siRNA and PGAamine polymers are water soluble and gave nice 28.11±7.35 nm particles when assembled via the microfluidic system in water (
The resulting solution however cannot be injected IV as is, and therefore 10% glucose solution was added to the polymer prior to assembly in order to obtain a 5% glucose concentration at the final injectable polyplex solution. Since DLS measurements revealed size dependency in both N/P ratio and component's concentrations (see, Table 5 above), N/P ratio was reduced to 1.5 and concentration to 1.5 mg/kg. This solution has maintained the narrow polydispersity and the desired diameter of 43±12 nm (see,
This injectable polyplex mixture was further evaluated for its morphology using TEM and Cryo-TEM, and shown in
Table 7 below presents a screen of N/P ratios and concentrations Vs. the obtained size of the formed polyplexes. siRNA was mixed with PGAamine K at the indicated N/P ratios and concentrations via a microfluidic chip. Size and PDI were measured by Zetasizer ZS.
Further activity assays were performed using the above formulation of PGAamine K, as follows.
Time Course Cellular Internalization of Formulated 1.5 N/P Ratio K:Cy5-Rac1 siRNA Polyplexes:
The uptake of PGAamine:Cy5-Rac1 siRNA 1.5 N/P ratio polyplexes was assessed by confocal microscopy, as shown in
Downregulation of Plk1 Expression and Inhibition of the Proliferation of MDA-MB-231 and MCF-7 Cells
The PGAamine K:Plk1 siRNA polyplexes were evaluated for their in vitro silencing activity using the artificial test system of Dual luciferase reporter, on both MDA-MB-231 and MCF-7 mammary adenocarcinoma cells and the obtained data is shown in
In order to evaluate the ability of the plk1 polyplexes to downregulate inherent protein's expression, the expression of Plk1 protein in MDA-MB-231 and MCF-7 cells following treatment with K:siPlk1 polyplexes was further tested by Western Blot analysis. Representative blot is shown on the left of
To demonstrate the ability of PGAamine K:siPlk1 polyplexes to inhibit mammary cancer cells growth, the effect of PGAamine K:Plk1 siRNA polyplexes treatment on the viability of MDA-MB-231 and MCF-7 cells was tested. Culture cells were treated with 50, 100 and 250 nM of siRNA for 72 hours. Cells were then trypsinized and counted. Number of cells was normalized to untreated cells. PGAamine K:plk1 siRNA treatment reduced the number of cells to 0.77, 0.66 and 0.53 folds of untreated cells in MCF-7 cells using 50, 100 and 250 nM concentrations respectively, and to 0.45, 0.26 and 0.31 folds of untreated cells in MDA-MB-231 cells using the same concentrations. Non-specific effect on the viability of cells was demonstrated in MDA-MB-231 cells, when PGAamine K:luciferase siRNA polyplexes reduced cells number to 0.84, 0.63 and 0.61 folds of the number of untreated cells. This non-specific effect, however, was weaker than the effect of the targeted PGAamine K:Plk1 siRNA polyplex on MDA-MB-231 cells (see,
Stability and Toxicity of K:siRNA Polyplexes.
K:siRNA polyplexes were evaluated for their compatibility to biological fluids.
The stability of PGAamineK:siRNA polyplexes in serum was also tested. Polyplexes were prepared at 1.5 N/P ratio and 1.5 mg/kg concentration and incubated with full FBS for the time course indicated above the gel image (see,
PGAamine K:siRNA polyplexes were further tested for their biocompatibility by an ex vivo red blood cell lysis assay (
K:Rac1 siRNA Polyplexes Accumulation in MDA-MB-231 Mammary Tumors and Silencing of Rac1 mRNA:
To further evaluate the ability of PGAamine to facilitate tumor accumulation of siRNA following systemic IV administration, the levels of siRNA in MDA-MB-231 mammary tumors were quantified using RT-PCR. 5 Nu/Nu tumor bearing mice were treated with 1.5 mg/kg PGAamine K:siRNA polyplexes for 3 sequential days, following by tumors resection on day 4.
The results demonstrate about 8 fold accumulation of Rac1 siRNA in mice treated with PGAamine K:Rac1siRNA polyplexes, while no Rac1 siRNA accumulation was noted in the tumors of mice treated with PGAamine:luciferase siRNA polyplexes (see,
To validate specific mRNA silencing in MDA-MB-231 tumor-bearing mice following the PGAamine K:Rac1 siRNA treatment regimen, both human-source (the tumor cells) and murine-source (the surroundings) mRNA levels of Rac1 were quantified. Both murine and human Rac1 mRNA levels were silenced to 0.04 and 0.08 folds respectively. Significant non-specific effect of luciferase siRNA was detected, with silencing to 0.43 and 0.59 folds in human and murine Rac1 mRNA levels respectively. See,
In order to follow the biodistribution of the polyplexes, PGAamine K:Cy5-Rac1 siRNA polyplexes were injected IV to 5 mCherry-labeled MDA-MB-231 mammary tumors bearing mice. Twenty four hours following a single injection of 1.5 mg/kg siRNA dose, mice were imaged and then organs were resected and quantified for Cy5 fluorescence. Due to the proximity in the absorbance and emission spectra of Cy5 and mCherry, a valid quantification of Cy5-siRNA tumor accumulation was not possible by this method, but tumor accumulation can be generally seen in
To demonstrate the targeted accumulation of PGAamine K:siRNA in an additional in vivo model, the polyplexes were IV injected at 4 mg/kg dose to A549 lung carcinoma SC tumor bearing mice. As shown in
PK measurements performed on the A549 tumor model revealed rapid clearance from plasma with a decrease to about 4% of the initial plasma level within 30 minutes, and to about 0.7% within 2 hours (see,
The significant accumulation of siRNA in tumors despite the rapid plasma clearance, indicates an efficient and fast tumor uptake.
The amphiphilic aminated poly(α)-glutamic acid (PGA) biodegradable polymeric nanocarrier (PGAamine) described herein was harnessed to provide a miRNA-siRNA combination treatment to target in parallel distinct molecular pathways activated in pancreatic cancer. siRNA was used to silence Polo-like kinase 1 (PLK1), a highly conserved serine-threonine kinase that is elevated in pancreatic ductal adenocarcinoma (PDAC), and miR-34a was introduced as a tumor suppressor miRNA which is downregulated in this cancer.
It was found that PGAamine-mediated delivery of PLK1-siRNA and miR-34a combination, effectively suppressed growth, clonogenicity and migration of human (MiaPaCa, Panc01, BxPC3), murine (Panc02) and transgenic (KrasLSL.G12D/+; p53R172H/+; PdxCretg/+(or KPC)) PDAC cells in vitro. Systemic administration of the polymer-miRNA-siRNA nano-sized polyplex to orthotopically-inoculated pancreatic tumors showed no toxicity and selective accumulation at the tumor site. This combination resulted in a synergistic antitumor effect and greater therapeutic efficacy than either monotherapies alone, suggesting an enhanced anticancer effect by inhibiting several key oncogenic pathways, amongst them a common target of PLK1 and miR-34a, myc.
Physico-Chemical Optimization of PGAamine K:miR-siRNA Nanoplexes:
Aminated poly(α)-glutamic acid (PGA) polymeric nanocarrier (PGAamine K) was synthesized by subsequently conjugating ethylenediamine and alkylamine moieties to the pending carboxylic groups of the PGA backbone, as described hereinabove for Polymer K. The resulting polymer (see,
To verify the ability of the polymer to form an electrostatic-based interaction with miRNA and siRNA, Nitrogen/Phosphate (N/P) ratios of polymer and miRNA-siRNA were incubated and the retardation of the small RNAs mobility on agarose gel was analyzed using electrophoretic mobility shift assay (EMSA).
Positively-charged PGAamine was able to bind miRNA-siRNA and neutralize their negative charge with an optimal N/P ratio of 2 (
The neutralization of the negatively charged miRNA-siRNA pair following mixture with the cationic carrier PGAamine was confirmed by surface charge measurements (zeta potential) of the polyplex and found to be almost neutral (4.68±3 mV,
Following cellular internalization, the small RNA oligonucleotides are expected to be released from the polyplex into the cytoplasm. Therefore, the ability of the polyplex to release miR-34a in increased amounts of the polyanion heparin using gel electrophoresis was tested (see,
The capability of the PGAamine-containing polyplex to release miRNA following incubation with cathepsin B, a thiol-dependent protease, which degrade PGA and is highly expressed in most tumor tissues, was attested. A gradual miRNA release from PGAamine-miR-34a polyplexes over time was observed following incubation with cathepsin B (2 Units/mg polymer,
The level of cathepsins activity (particularly cathepsin B) in pancreatic tumor xenograft tissues was profiled. For this purpose, Cy5-labeled GB123 activity based probe was used. As a control for specificity of labeling, a potent active-site cathepsin inhibitor GB111-NH2 was used prior to incubation with the Cy5-labeled GB123 probe. As depicted in the fluorescent microscopy images, high expression levels of active cathepsins were found in the pancreatic tumor tissue. On the other hand, no considerable expression was observed in the normal adjacent tissue, as well as in the negative control (
Cellular Internalization of PGAamine-siRNA Nano-Polyplexes:
The ability of Cy5-labeled siRNA complexed with PGAamine to internalize into human MiaPaCa2 PDAC cells was tested. Confocal images of cellular uptake kinetics for cells incubated with Cy5-siRNA-PGAamine polyplexes for 4, 24 and 48 hours are depicted in
To evaluate the cellular localization of the polyplex and to eliminate optical artifacts, z-scan (
Further examination of cellular internalization of siRNA-PGAamine polyplex was performed in live MiaPaCa2 cells using the ImageStream multispectral imaging flow cytometer. Live cells were monitored 24 hours after transfection, using Cy5-labeled siRNA (
The amount of cells that internalized the polyplex was shown also by the internalization histograms,
The intracellular uptake was investigated and it was found that the two distinct cell morphologies of MiaPaCa2 possess different pattern of siRNA uptake. According to the ATCC, MiaPaCa2 cells have two morphologies: One is attached epithelial cells and the other is floating rounded cells. It was found that the attached, larger cell population in size (R4) internalized Cy5-siRNA-PGAamine polyplexes, while the smaller in size cell populations (R3 and R2) did not (data not shown). The same intracellular uptake pattern was observed using Lipofectamine™ 2000 as a transfection reagent, indicating that in live MiaPaCa2 cells siRNA uptake is achieved mostly by the adherent large cell population.
The transfection efficiency into other pancreatic cancer cell lines, using Cy5-labeled PGAamine, was investigated. Flow cytometry data showed that polyplexes (3.5 μg mL−1 Cy5-PGAamine complexed with 100 nM siRNA) were able to transfect 86.64±4.4% of KPC cells, 97.43±3.07% of Panc02 cells, 46.76±2.7% of Panel cells and 93.78±4.6% of BxPC3 cells (data not shown).
Nano-Polyplexes Cellular Trafficking:
Further insight into the trafficking and intracellular distribution of PGAamine-siRNA polyplex was gained by confocal microscopy analysis (see,
Biocompatibility of PGAamine-siRNA Polyplexes:
In order to evaluate the safety profile of PGAamine K as a nanocarrier, an ex vivo cytokines induction assay was performed using human PBMCs, which determined the secretion level of important inflammatory cytokines, IL-6 and TNF-α, as a model for the innate immune response. For this purpose, freshly isolated PBMCs were seeded in 6-well plates and treatments of PGAamine alone or complexed with several concentration of siRNA (40, 200 and 400 nM) was added to the PBMCs. Following 24 hours of incubation, supernatants of the cells were collected and human IL-6 and TNFα cytokines were measured by ELIZA.
Neither PGAamine alone nor PGAamine-siRNA polyplex induce elevated secretion of the cytokines tested (see,
Stability of polyplex was tested in vitro in 100% fetal bovine serum (FBS). There was no release of miRNA from polyplexes up to 12 hours of incubation. Moreover, PGAamine polymer stabilized miR-34a against serum degradation for a much longer time (12 hours) compared to the naked miR-34a (see,
To determine the in vivo toxicity and maximum tolerated dose (MTD) of PGAamine-miRNA polyplexes, the viability of Balb/c mice was tested and monitored for a period of 5 weeks, following a single intravenous injection of the polyplex at various miRNA dosages (6, 8, 10 and 12 mg/kg). The mice were viable following all miRNA dosages that were injected, up to 12 mg/kg siRNA-equivalent dose (see, Table 8 below).
The polyplexes effect on mouse normal pancreas and on glucose levels in mouse blood was assessed. Following 3 sequential i.v. injections of PGAamine-miR-34a (2 mg/kg miRNA dose) polyplexes or PBS, blood glucose levels were measured from the mice tail and pancreas was resected, embedded in paraffin and stained with Hematoxylin and Eosin. No differences in normal pancreas morphology as well as in blood glucose levels were observed between PBS treated and polyplex treated mice (data not shown).
In Vitro Efficacy of miRNA-siRNA Delivery and their Combination Effect:
To confirm in vitro miRNA and siRNA delivery efficacy, PGAamine polymer carrying separately, miR-34a or PLK1-siRNA, at the optimal N/P ratio of 2, was applied to cultured MiaPaCa2 cells and the levels of the miR and its target genes as well as the levels of PLK1 mRNA and protein were quantified using real-time qRT-PCR and western blot analyses.
There was a significant elevation in miR-34a levels following transfection with the PGAamine-miR-34a polyplexes compared to the untreated cells and NC-miR-treated cells, with a 929 fold change increase after 72 hours, as shown in
Transfection with NC-miR had no significant effect on the expression levels of the investigated target genes. Transfection of cells with PGAamine-PLK1-siRNA polyplexes was also efficient and silenced PLK1 by 50% and 80% at mRNA and protein levels, respectively (see,
The ability of miR-34a and PLK1-siRNA, complexed with a PGAamine nanocarrier, to affect the tumorigenisity of pancreatic cancer cells was tested. Cells were transfected with serial concentrations of PGAamine-polyplexes containing miR-34a or PLK1-siRNA alone and viable cells were counted by Coulter Counter. Both, miR-34a alone (see,
Cell migration was studied using a wound closure assay in which cells were allowed to grow in a 96-well ImageLock plate until confluency and a wound was created using a 96-pin woundmaking tool (WoundMaker™). The cells were then incubated with the PGAamine-miR-siRNA polyplexes and wound closure was monitored using IncuCyte® ZOOM Live-Cell Analysis System.
Cells treated with NC-miR and NC-siRNA together and cells that left untreated, closed the wound almost completely (about 80%) within 48 hours (see,
The effect on growth and survival of pancreatic cancer cells was assessed also using clonogenic assay. MiaPaCa2 and KPC cells were transfected with miR-34a or PLK1-siRNA (100 nM) separately or combined using PGAamine K for 24 hours. Transfected cells were seeded in 35 mm plates in triplicates for 8-10 days and stained with crystal violet to determine the number of surviving colonies. miR-34a-PLK1-siRNA combination (100 nM each) reduced the number and size of surviving colonies of the pancreatic cancer cells (by 64%) compared to the untreated cells (
To validate the synergistic effect of miR-34a-PLK1-siRNA combination treatment using the PGAamine nanocarrier, its effect on the murine pancreatic cancer cell line, KPC was studies. It was found that although, only PLK1-siRNA alone and not miR-34a alone significantly reduced the viability of KPC cells, the combination treatment of both of the small RNA oligonucleotides showed synergistic reduction in cell viability as analyzed using the additive model (data not shown). In addition, KPC cells treated with the combination closed only 33% of the wound compared to the untreated cells and to the NC-miR/NC-siRNA treated cells that closed the wound almost completely (data not shown). miR-34a/PLK1-siRNA combination reduced the number and size of surviving colonies of the KPC cells (by 72%) compared to the untreated cells (data not shown). These results indicate that PGAamine carrying miR-34a-PLK1-siRNA combination could inhibit pancreatic cancer cells growth, migration and survival effectively.
Biodistribution and Tumor Accumulation of PGAamine-siRNA Polyplexes in Mice:
To assess whether PGAamine nanocarrier exhibit preferable accumulation at the tumor site once injected systemically, an orthotopic pancreatic cancer mouse model was developed by injecting mCherry-labeled MiaPaCa2 cells into the pancreas of SCID mice. First, cells were infected with a pQC-mCherry retroviral vector, as previously described. Then, mCherry-labeled cells were injected orthotopically to the pancreas and tumor growth rate was monitored by fluorescence using a non-invasive intravital imaging system (CRI Maestro™). Two weeks post injection, tumors were observed with increase in signal until day 31 (data not shown). mCherry fluorescent signal was found only in the pancreas (data not shown).
To study the pharmacokinetics profile of nano-polyplexes, mice bearing orthotopic mCherry-labeled tumors (with a fluorescent signal of about 1000 scaled counts/s) were administered via the tail vein with PGAamine-Cy5-siRNA polyplexes (0.5 mg/Kg siRNA, 100 μl) or with Cy5-siRNA alone and imaged at 10 minutes, 1, 3 and 24 hours thereafter in the Maestro.
As shown in
For biodistribution examination, tumors were and healthy organs (heart, lungs, liver, kidneys and spleen) were resected from mice, 24 hours following intravenous administration of Cy5-labeled siRNA alone or complexed with PGAamine and measured Cy5 fluorescent intensity. As shown in
Quantification of Cy5 component revealed a 5-fold increase in total signal (scaled counts/sec)/tissue weight of the siRNA complexed with PGAamine compared to siRNA alone at the tumor site (see,
In addition, the vasculature functionality and morphology of the pancreatic cancer tumor from the orthotopic xenograft mouse model was evaluated. It showed enlarged unorganized leaky blood vessels as compared to normal pancreas (data not shown).
The accumulation of miR-34a in the orthotopic PDAC tumors following 3 sequential IV injections of PBS or polyplex formulated with miR-34a or NC-miR (n=4 mice per group, 2 mg/kg miR dose) was further tested. As shown in
miR-34a target genes levels, from the same isolated tumors, were quantified by Real-Time RT-PCR. In tumors from miR-34a-treated mice, Bcl2, CDK6, MET and Notch1 levels were reduced by 45, 25, 20 and 11% relative to NC-miR treated mice (see,
In Vivo Anti-Tumor Effect of miR-siRNA Combination:
To determine the therapeutic effects of combined miR-34a and PLK1-siRNA delivery in vivo, tumor-bearing mice, 14 weeks following cells inoculation, were randomized into four treatment groups (n=6/7 mice per group): (i) miR-34a/PLK1-siRNA, (ii) miR-34a/NC-siRNA, (iii) PLK1-siRNA/NC-miR, and (iv)NC-miR/NC-siRNA, and a group treated with PBS. Mice were IV injected with a total small RNA dose of 3.0 mg/kg every day, five consecutive times, for two rounds with a 3 days break between them.
Tumor growth monitoring using intravital fluorescent imaging revealed that miR-34a/PLK1-siRNA combination therapy induced pancreatic tumor regression, inhibiting tumor growth to an average of 3.85% (11.3±39 scaled counts/sec, P<0.01) compared to tumors treated with PBS (see,
During this efficacy study, at day 33 from tumor inoculation, an image of representative mouse from each treatment group was taken in the CRI-Maestro, in which the differences in tumor signal can be seen (see,
All animals tolerated small RNA therapy well, with no significant weight loss observed after administration of all treatments (see,
The effects of the treatments on blood counts and chemistry were also studied. For that, blood was withdrawn from PBS and PGAamine-small RNA oligonucleotides-treated mice, on day 23 from treatment initiation. All treatments did not affect either blood counts (data not shown) or blood chemistry parameters (see, Table 9 below). Survival of mice treated with the combination was significantly (P<0.05) prolonged compared to all other treatment groups (see,
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IL2016/051071 | 9/30/2016 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62234819 | Sep 2015 | US |
