Patent Grant
7425543
The present invention relates to the field of drug delivery systems. Specifically, the present invention relates to methods for preparing microencapsulated drugs using non-antigenic, biodegradable materials and also to microencapsulated compositions that are targeted to phagocytic cells such as macrophages, endothelial cells, Kupffer cells, dendritic cells and the like, or a diseased organ (such as the liver, kidneys, lungs, heart, spleen), or a diseased site (such as tumors, arthritic joints), which digest the biodegradable coating, releasing the intact drug or active component either intracellularly or at the site of accumulation. Such compositions are useful in the treatment and prevention of diseases.
Microencapsulation of water-soluble compounds contained in albumin microspheres (“MS”) has been demonstrated by our laboratory (and disclosed in previous co-pending applications) to target phagocytic cells such as macrophages/monocytes, which produce the majority of the pro-inflammatory cytokines. This technique has been demonstrated to improve the efficacy of cytokine inhibiting compounds such as neutralizing antibodies. We have further evaluated the method of preparation of albumin microspheres containing other categories of drugs such as CNI-1493 (a guanylhydrazone compound which inhibits p38 MAP kinase), clodronate (a bisphosphonate), antioxidants such as pyrrolidine dithiocarbamate, and antisense oligomers to NF-kB. Microencapsulation of these compounds has improved inhibition of cytokines such as TNF, and IL1-beta in an in-vitro whole blood model, endotoxin shock model, and a bacterial septic shock model. We also have evaluated the preparation and completed the efficacy testing of a melanoma vaccine preparation, which worked very well in preventing tumors in mice.
In a first embodiment of the present invention the various process parameters, materials and reaction conditions of the emulsification methodology previously developed (and described in the copending application(s) cited above) are expanded.
Drug delivery to specific diseased sites can aid in reducing side effects in patients, thereby preventing toxicity. By using drugs in a microencapsulated form, exposure of the drug to non-diseased organs and tissue can be prevented.
A methodology to produce microencapsulated monoclonal antibodies by the emulsification method, with the use of olive oil as the emulsification media, has been previously disclosed in the copending application(s). We disclose herein additional data after evaluating bioactive protein drugs, namely, anti-sense oligonucleotides to NF-kB, in several different oils as the emulsification media, and under different temperatures and we have also evaluated the process with the use of different aqueous solvents to dissolve the drugs.
In a second embodiment of the present invention microspheres are prepared by a novel nebulization method with different examples of drugs, different solvents, different temperatures and methodology variations.
Other classes of drugs evaluated using this emulsification method are as follows:
In this embodiment we have evaluated different solvents, different temperatures and methodology variations. The drug evaluated with this nebulization method is the anti-sense oligonucleotides to NF-kB.
In a particular embodiment, the present invention provides a method of encapsulating a bioactive material by nebulization, comprising:
The above delivery system shows that the anti-sense oligonucleotides to NF-kB can be used very effectively to inhibit cytokine-mediated processes involving phagocytic cells such as macrophages, white cells dendritic cells and endothelial cells. From these studies several other applications are relevant as follows:
A) Cytokine Related Diseases:
B) Vaccine Delivery System:
C) Anti-Tumor Sustained Drug Delivery System:
Sustained release of therapeutic agents for the treatment of cancer is appealing considering the fact that therapy is usually long-term. It offers the possibility of using lower doses to achieve similar therapeutic effects as conventional non-sustained dosage forms. With the advent of biotechnology and the advances in the techniques of molecular biology, our antitumor arsenal has rapidly expanded to include protein drugs, peptides and cytokines. These new weapons, although potent, still need suitable delivery systems. Being protein in nature, these agents may be targets of enzymes in the blood. As a result injecting these agents requires very high doses which are not only cost prohibitive, but also potentially dangerous. Interleukin-12 is a recently discovered heterodimeric cytokine. It has been shown in various animal models of cancers to have tremendous antitumor potential. Using genetically engineered fibroblasts, it has been demonstrated that sustained presence of lower concentrations of IL-12 produce the same antitumor effects as larger concentrations that are not sustained. However, it is not easy to produce genetically engineered cells and is even more difficult to adapt it for mass therapy in general due to the considerations of cost and the amount of labor involved. Better alternatives exist in the form of particulate drug delivery systems such as microspheres that can not only shield such protein drugs from the enzymes in the blood, but can also sustain their release. Microspheres also have the added advantage of large scale production in addition to being amenable to preparation using a wide variety of biodegradable polymers.
We have evaluated the use of biodegradable albumin microspheres to sustain the release of IL-12. When administered intraperitoneally to C57BL/6 mice bearing subcutaneous melanomas, the microspheres significantly prolonged the survival when administered at half the weekly dose of the solution formulation. The microsphere dosage form also resulted in generally lower levels of liver and kidney function enzymes, suggesting lower toxicity.
D) Transfection System:
The microspheres can be used as an effective tool for transfection of genetic material into cells. Some of the current methods of cell transfection result in a significant number of cell deaths during transfection processes such as microporation. Since the microspheres used in our studies are less than 1 micron in size, they are readily taken up into the cells and can transfer the drug/material within the microspheres directly into cells.
Other features and advantages of the present invention will become apparent upon reading the following detailed description of embodiments of the invention, when taken in conjunction with the appended claims.
The invention is illustrated in the drawings in which like reference characters or references designate the same or similar parts or parameters throughout the figures (unless otherwise noted) of which:
We will first describe the expansion of the emulsification methodology originally disclosed in prior copending application(s).
We have further expanded the testing of microspheres prepared with different drugs, oils, at different process temperatures, different aqueous solvents used to dissolve the drug and have also evaluated variations in methodology of manufacture based on the initial patent application wherein the microspheres were prepared with monoclonal antibodies to cytokine antagonists using albumin as the polymer matrix and olive oil as the emulsifying media by the emulsification methodology.
Example 1 describes encapsulation by emulsification of a representative bioactive protein, namely the anti-sense oligonucleotides to nuclear transcription factor NF-kB. Process parameter expansion included the testing of canola oil, cottonseed oil and mineral oil. The results showed that the oils tested performed well. Other bioinert vegetable and other oils, such as but not limited to, sunflower, safflower, soybean, palm, palm kernel, coconut, caster, peanut, gingley, fish, sesame, rice bran, and the like, depending on particular bioinert characteristics, and subcomponents thereof, such as, but not limited to, monounsaturated (MUFA), polyunsaturated (PUFA) and essential fatty acids (EFA), as well as mixtures of the foregoing. Other mineral oils, including, but not limited to, heavy, light and various subfractions and combinations thereof are contemplated as being within the scope of the present invention.
The temperature range of the solvent cooling was tested and broadened. Temperature range of 5-40 degrees C. was tested and found to produce acceptable results. Temperatures below about 5 degrees C. may result in at least partial freezing of aqueous components and may be undesirable.
Further, the selection of aqueous phase was expanded to now include, but not be limited to, water, phosphate buffered saline, water plus Tween® 80, and saline.
Example 2 describes the formation of microspheres of a representative tumor vaccine drug, namely, extracellular antigen, and the bioactivity obtained.
Example 3 describes the formation of microspheres of an aqueous soluble drug, namely, CNI-1493, a guanylhydrazone, and the bioactivity obtained. The test results showed that the CNI-1493 microencapsulated form using the method of the present invention was more efficacious than the corresponding doses of the soluble, non-encapsulated form in attenuating endotoxin or cytokine release.
Example 4 describes the formation of microspheres of a representative chemical drug, namely, clodronate, a bisphosphonate, and the bioactivity obtained.
Example 5 describes the formation of microspheres of a representative bioactive protein, drug, namely, anti-sense oligonucleotides to NF-kB, and the bioactivity obtained.
Example 6 describes the formation of microspheres of anti-sense oligonucleotides to NF-kB by the novel nebulizing method of the present invention, and the bioactivity obtained.
The invention will be further described in connection with the following examples, which are set forth for purposes of illustration only. Parts and percentages appearing in such examples are by weight unless otherwise stipulated. It is to be noted that unless otherwise stated the method of forming the microspheres used olive oil.
Clinical Application in Septic Shock:
Formulation and Testing of Antisense Oligomers to NF-KB
A) Introduction
NF-kB is a nuclear transcription factor, which exists in the cytosol in an inactive form complexed to IkB. Endotoxin stimulates intracellular mediators, which results in phosphorylation of IkB producing translocation of NF-kB to the nucleus with subsequent activation of DNA. The mRNA for the synthesis of multiple pro-inflammatory mediators including TNF, IL1 and IL6 is rapidly produced. We have found that microencapsulated antisense oligomers (MSASO) to the p65 subunit of NF-kB inhibits TNF, IL1 and IL6 in-vitro. Antisense compounds have the potential to be very useful therapeutic agents by virtue of their ability to inhibit specific protein synthesis. However, a limiting factor of antisense therapy has been difficulty in obtaining adequate intracellular penetration by these large compounds. Our previous work has demonstrated improved effectiveness in cytokine inhibition using antisense to NF-kB by microencapsulated intracellular delivery. Microencapsulation provides improved delivery of the antisense compound as intracellular oligonucleotides are rapidly transported to the nucleus. Our previous studies have confirmed this hypothesis by greatly improving the effectiveness of microencapsulated antisense to the p65 moiety of NF-kB in a rat model of endotoxic shock and sepsis.
B) Preparation of the Anti-Sense Oligonucleotides to NF-kB by Albumin.
1) 50 mg of human albumin was dissolved in 2 cc of one of pyrogen free water.
2) The antisense oligonucleotides (oligomers) to NF-kB was separately solubilized in phosphate buffered saline (PBS) at a concentration of 25 mg/cc.
3) The above two solutions were mixed together for approximately 30 minutes.
4) The resulting mixture was cooled to 5 degrees C.
5) 20 cc of olive oil was taken in a 50 cc beaker and cooled to 5 degrees C. and maintained at that temperature in an ice bath.
6) The mixture of albumin and oligonucleotides was added to the oil and emulsified with the aid of a Branson Sonifier at medium setting for 20 minutes.
7) The emulsion containing the microencapsulated albumin-drug microspheres were evaluated for size with the use of a laser particle sizer until the microspheres were about 1 micron in diameter.
8) The microspheres were cross-linked with 0.5 cc of a 25% w/v solution of glutaraldehyde for 1 hour with constant stirring using a tissue homogenizer at high setting while maintaining the temperature at approximately 5 degrees C. with the aid of an ice bath.
9) The microspheres were washed with three 20 cc washes of methanol and finally sized while being suspended in the final methanol wash, with the aid of sequential HPLC filters (50, 20, 10, 5, and 1 micron size).
10) The microspheres were freeze dried and stores in a refrigerator until used.
In all cases the microspheres were suspended in pyrogen free water or saline before use.
The above procedure was repeated in order to evaluate to use of different types of oils as the emulsifying media, and different temperatures on manufacture were also evaluated in addition to the 5 degree C. described above. Finally, in addition to water, different solvents were also evaluated as the media for dissolution of the drug. The specifics of each of the parameters evaluates are as follows:
a) Effect of Different Oils:
Different oils such as canola oil, cottonseed oil and mineral oil were used for the study and was compared to olive oil used previously for the manufacture of the microspheres. It is to be understood that any bioinert vegetable or mineral oil can be used.
b) Effect of Different Temperatures:
The microspheres were prepared under wide variations of temperature such as 5, 10, 30 and 40 degrees C. The method of the present invention can thus be performed at a temperature range of from about 5-40 degrees C.
c) Effect of Different Aqueous Phase used to Dissolve the Drug:
In addition to water, and phosphate buffered saline (PBS), water containing Tween™ 80 (polyoxyethylene sorbitan monooleate, available from ICI Americas, Inc.) and saline were used to examine if differences would be significant.
Drug content analysis and efficacy studies evaluating TNF-alpha suppression was conducted using the In-vitro Whole Blood Model. The following variations in the manufacture procedure were evaluated.
C) Experimental Method:
Drug content analysis was determined by HPLC methods developed in our laboratory.
The preparations were evaluated for drug efficacy with the aid of the whole blood model, briefly outlined as follows:
Blood was pooled into lavender top tubes containing EDTA. The blood was separated into three 5 ml aliquots and pre-treated for 1 hour with one of the following batches of microspheres and challenged with endotoxin (100 mcg/ml). Samples were be obtained at 0 and 4 hours post endotoxin challenge to determine the TNF-alpha levels. The efficacy of the cytokine suppression due to the addition of microencapsulated oligomers to NF-kB was compared to microspheres prepared using olive oil as described in the copending patent application.
D) Results:
Effect of Different Oils on Drug Content Analysis:
Effect of Temperature Variations on Drug Content Analysis:
Effect of Different Aqueous Phases Used on Drug Content Analysis:
Effect of Different Oils on TNF-Alpha Suppression:
Effect of Temperature Variations on TNF-Alpha Suppression:
Effect of Different Aqueous Phases Used on TNF-Alpha Suppression:
Tumor Vaccine Drug
Tumor Protection Studies Using Microparticle as Adjuvant or Coadjuvant in a Tumor Vaccine
A) Introduction
The induction of an immune response is a complex and intricate process requiring an intact immune system to evaluate. Thus, a mouse tumor model was used to evaluate the microencapsulated extracellular antigen (MECA) vaccine preparation. The antigens used in the vaccine were derived from the B16 murine melanoma cells growing in culture. The C57BL/6 mouse, syngeneic to the B16 murine melanoma cells, was used. This represents a prophylactic tumor vaccine where the mice were first vaccinated to induce an anti-tumor response. The mice were then challenged to determine if an anti-tumor response was induced with the capacity to reject the establishment of the murine melanoma.
B) Preparation of Melanoma Vaccine Preparation.
The microencapsulated vaccine preparation was made according to the method described in Example 1.
C) Experimental Methods
Immunization and Tumor Protection Studies
MECA (containing 20 μg ECA in a total of 80 μg MECA) and blank MP (microparticles) were prepared by a water-in-oil emulsion cross-linking technique using glutaraldehyde as the cross linking agent. To evaluate the anti-tumor effect of 20 μg extracellular antigen in an equivalent amount of microparticles used in the first study (80 μg MECA total), 3 groups of female C57BL/6 mice (n=5), 8-12 weeks old, were vaccinated, subcutaneously. The three groups were vaccinated with 20 μg of extra-cellular antigen (ECA) contained within a total of 80 μg of microencapsulated extracellular antigen (MECA), resuspended in a total volume of 100 μl with PBS, extra-cellular antigen in solution (ECA soln) in PBS and blank microparticles (Blank MP) in PBS, respectively. The mice were boosted every week for 3 weeks for a total of 4 injections. 7 days after the last boost the mice were challenged with 7×105 live B16 melanoma cells subcutaneously at a contralateral site, as described above. The mice were then observed for 60 days for the development of tumors and tumor size and tumor incidence was recorded.
D) Results and Discussion
Female C57BL/6 mice were vaccinated with MECA (20 μg ECA contained in 80 μg total MECA), blank MP or ECA soln subcutaneously. After the first vaccination the mice were boosted once a week for three weeks. Seven days after the last vaccination boost the C57BL/6 mice were inoculated at a distant site with 7×105 live syngeneic B16 melanoma cells. The mice were subsequently monitored for the development of tumors and tumor incidence was reported (
The studies suggest that microencapsulating tumor antigens could have an adjuvant effect in inducing tumor immunity by targeting professional antigen presenting cells. In addition, the results of the blank microparticle group of 40% tumor free at 60 days, suggests that BSA microparticles could possibly be an excellent adjuvant for the B16 melanoma due to the homology between BSA and the B700 tumor antigen.
E) Conclusion.
The in vivo dose response studies revealed that the vaccine dose of 20 μg ECA contained in 80 μg of total MECA worked very well in this study. This dose of the MECA vaccine resulted in C57BL/6 mice remaining 80% tumor free up to the 60-day study period. The studies suggest that microencapsulating tumor antigens could have an adjuvant effect in inducing tumor immunity by targeting professional antigen presenting cells. In addition, the results of the blank microparticle group of 40% tumor free at 60 days, suggests that BSA microparticles could possibly be an excellent adjuvant for the B16 melanoma due to the homology between BSA and the B700 tumor antigen.
The B16 murine melanoma tumor represents a very rigorous tumor model. For this reason it is possibly more representative of cancer in the human situations. These results do indicate that the microparticle induces a greater anti-tumor effect.
Chemical Drug, CNI-1493: a Guanylhydrazone Compound
Application in Septic Shock
Formulation and Testing of Microencapsulated CNI-1493.
Prevention of Lethality and Suppression of Pro-Inflammatory Cytokines in Experimental Septic Shock by Microencapsulated CNI-1493
A) Introduction
Endotoxemia in animals is associated with the release of pleiotropic cytokines such as TNF-alpha and IL-1-beta from the activated macrophages and polymorphonuclear cells. Experimental drugs that inhibit the effect of these cytokines such as monoclonal neutralizing antibodies (TNF-alpha monoclonal antibody), receptor antagonists (IL-1 receptor antagonist) and receptor fusion proteins have been evaluated in animals and in the clinic for their efficacy in septic shock. Recently, a newly developed water soluble tetravalent guanylhydrazone compound termed “CNI-1493” (N,N′-bis[3,5-diacetylphenyl]decanediamide amidinohydrazone tetrahydrochloride) was shown to be efficacious in reducing lipopolysaccharide (LPS) induced TNF-alpha, IL-1-beta and IL-6 release and lethality in animals.
We have previously reported studies, which demonstrated microencapsulation of cytokine neutralizing antibodies increased their efficacy compared to the soluble form in various in vitro and in vivo disease models. Similarly, microsphere form of other cytokine antagonists may also be more efficacious than the corresponding soluble form because of the targeted uptake of the microencapsulated drugs by macrophages. In this Example, we evaluated the efficacy of microsphere form of the newly developed compound CNI-1493 by Cytokine Network Incorporated. Comparison of efficacy of the soluble and microencapsulated form of CNI-1493 was evaluated using an in vitro endotoxin-induced cytokine release whole blood model, and an in vivo model of endotoxemia and E. Coli-induced peritonitis.
B) Preparation of CNI-1493 Microspheres.
The microencapsulated CNI-1493 preparation was made according to Example 1.
C) Experimental Methods
For each sample (n) blood was collected in EDTA (1.5 mg for each ml of blood) from five rats and pooled. After a baseline plasma sample the blood was aliquoted into five groups. There were six replicates in each group. Each group received one of the following treatments: saline or soluble form of CNI-1493—0.25, 0.5 or 1.0 microgram/ml or blank microspheres (MC) or MC form of CNI-1493—0.25, 0.5 or 1.0 microgram/ml. All groups were incubated at 37 degrees C. under an atmosphere containing 5% CO2. After two hours of incubation, endotoxin (100 ng/ml) 0113 obtained from Escherichia Coli (Associates of Cape Cod, Wood Hole, Mass.) was added to all groups and incubated for an additional 24 hours. Plasma samples were periodically collected at 2, 4, 6 and 24 hours after endotoxin for measurement of TNF-alpha and IL-1-beta using a modified alkaline phosphatase ELISA technique.
D) Results and Discussions
Endotoxin-induced cytokine release in whole blood model: Effect of CNI-1493 on endotoxin-induced TNF-alpha and IL-1-beta release is shown in
In vivo model of endotoxemia: The survival data is shown in Table 1.
All the animals that received 1, 2, 5 mg/kg of soluble form of CNI-1493 died within 24 hours of endotoxin while 50% of the animals that received 10 mg/kg of soluble form of CNI-1493 and 25% of the animals in the group that received 1 mg/kg dose of MC form of CNI-1493 survived for seven days after endotoxin. On the other hand, all the animals (100%) in the group that received 2, 5, and 10 mg/kg of the MC form of CNI-1493 survived for seven days after endotoxin. The cytokine levels for this study are shown in
E. Coli-induced peritonitis model of septic shock: The survival data is shown in Table 2.
E. Coli + saline
E. Coli + blank microspheres
E. Coli + 2 mg/kg Sol
E. Coli + 2 mg/kg MC form
E. Coli + 2 mg/kg Sol.
E. Coli + 2 mg/kg MC form
E. Coli + 5 mg/kg Sol.
E. Coli + 5 mg/kg MC form
E. Coli + 5 mg/kg Sol.
All the animals that received saline or blank MC or 2 mg/kg of soluble form of CNI-1493 or 5 mg/kg of soluble CNI-1493 or 2 mg/kg of MC form of CNI-1493 pretreatment died within 4 to 8 hours of E. Coli administration. There was minimal protection against lethality with a 17% survival rate after treatment with either 5 mg/kg of MC form of CNI-1493 or a 2 mg/kg of a soluble form of CNI-1493 and gentamycin. Administration of gentamycin also increased the survival rate to 50% in the group that received 5 mg/kg of soluble form of CNI-1493 pretreatment, 67% in the group that received 2 mg/kg MC form of CNI-1493 and to 83% in the group that received 5 mg/kg MC form of CNI-1493. Both soluble and MC form of CNI-1493 lowered E. Coli-induced TNF-alpha and IL-1-beta levels and the MC form of CNI-1493 was significantly better than the soluble form of CNI-1493 in attenuating E. Coli-induced TNF-alpha and IL-1-beta levels.
Microencapsulation of CNI-1493 improved effectiveness in both the in vitro and in vivo models. The results show that MC form of CNI-1493 was more efficacious than the corresponding doses of soluble form of CNI-1493 in attenuating endotoxin or E. Coli induced cytokine release and lethality. In previous studies using microencapsulated cytokine neutralizing antibodies, we saw an improvement in efficacy in inhibition of endotoxin-induced cytokine release and prevention of lethality due to endotoxin or E. Coli-induced peritonitis compared to the corresponding soluble form of the neutralizing antibodies. It may be that the effectiveness of microencapsulated compounds (excluding the sustained release form) is magnified by the intracellular release in phagocytic cells. CNI-1493 released from the microspheres after being phagocytozed by phagocytic cells provides a higher intracellular concentration that leads to effective suppression of the proinflammatory cytokines by an intracellular mechanism of action. Previous studies have shown that soluble CNI-1493 can suppress LPS induced cytokines such as TNF-alpha, IL-1-beta and IL-6 from peripheral blood monocytes as seen in this study. The mechanism by which CNI-1493 inhibits TNF-alpha synthesis is speculated to be at the translational or post-translational level. In this study MC form of CNI-1493 strongly inhibited endotoxin-induced TNF-alpha and IL-1-beta levels while the soluble form of CNI-1493 inhibited endotoxin-induced TNF-alpha and IL-1-beta levels to a smaller extent both in the in vitro and in vivo models. The extent of endotoxin-induced TNF-alpha inhibition by the lowest dose of MC form of CNI-1493 (0.25 microM) was similar to that produced by the highest dose of soluble form of CNI-1493 (1.0 microM) in the in vitro whole model. This indicates that theoretically the MC form of CNI-1493 could be at least four times as potent as the soluble form of CNI-1493 in inhibiting endotoxin-induced TNF-alpha synthesis.
MC form of CNI-1493 (2 mg/kg) provided complete protection against lethal endotoxemia while there was no survival with the same dose of soluble form of CNI-1493 (2 mg/kg) or a only 50% survival with five times higher dose of the soluble form of CNI-1493 (10 mg/kg). Complete protection by the MC form of CNI-1493 against lethality due to endotoxemia suggests a greater effectiveness of the microencapsulated delivery system. At a dose of 5 mg/kg of CNI-1493, the survival rate in E. Coli-induced peritonitis model was also much higher with the combination of gentamycin and MC form of CNI-1493 (83%) compared to the combination of gentamycin and soluble form of CNI-1493 (50%). In this infectious model of lethality both soluble and MC form did not prevent lethality except when gentamycin was used in conjunction with CNI-1493. This indicates that antibiotic treatment is essential in a severe infectious state. The experimental model of peritonitis has proven to be resistant to treatment with antibiotics alone or soluble form of TNF-alpha neutralizing antibodies alone. In fact, there has been no previously reported studies that demonstrate improved survival in this model after treatment with the soluble form of cytokine antagonists except when treated with a combination of antibiotics and microencapsulated cytokine antagonists.
In conclusion, we have demonstrated the superior effectiveness of microencapsulated CNI-1493 in suppressing endotoxin-induced TNF-alpha and IL-1-beta release using an in vitro whole blood model. This improved effectiveness has produced significantly better survival in both endotoxemia and E. Coli peritonitis model of septic shock.
Chemical Drud-Clodronate
Application-Glomerulonephritis
Macrophage Depletion by Albumin Microencapsulated Clodronate: Attenuation of Cytokine Release in Macrophage Dependent Glomerulonephritis
A) Introduciton
The macrophage plays an important role in the inflammatory process through the release of cytokines, chemokines and other substances. The role of macrophage in various inflammation-mediated disease states can be evaluated by depletion of macrophages with clodronate, a water soluble compound. Clodronate, a bisphosphonate, is a potent inhibitor of osteoclast-mediated bone reabsorption and clinically used to treat metabolic bone diseases. Clodronate in free (solution) form has little effect on macrophage function following systemic administration. However, liposomes containing clodronate are readily phagocytozed by macrophages and cause depletion of macrophages in the liver, spleen, lymph nodes and peritoneal cavity, and monocytes in the systemic circulation. We have developed a method of microencapsulation of clodronate using albumin that has several advantages over the use of liposomes. Albumin can be used as the biocompatible polymer matrix to form microspheres (MS) of varying size which has greater stability and ease of preparation when compared to liposomes. Albumin is a biodegradable, non-toxic substance that has a high efficiency of encapsulation. The purpose of this investigation is to determine if albumin MS containing clodronate: 1) will produce systemic macrophage depletion, 2) have an effect on TNF-alpha and IL-1-beta release induced by endotoxin in vitro, and 3) have an effect on macrophage infiltration in experimental glomerulonephritis (GN) in rats. The results indicate that clodronate MS effectively depleted macrophages, attenuated endotoxin-induced TNF-alpha and IL-1-beta release, and blocked experimental GN induced macrophage infiltration into the glomerulus.
B) Preparation of Microspheres.
The microencapsulated clodronate was made according to Example 1.
C) Experimental Methods
D) Results and Discussion
Our study demonstrated that small doses of clodronate encapsulated in albumin are effective in depleting ED1 positive macrophages from the liver, spleen, kidney and peripheral blood in rats. Clodronate MS also produced a prompt reduction in endotoxin stimulated TNF-alpha and IL-1-beta release which was significantly greater than clodronate in free (solution) form and prevented macrophage infiltration into the glomerulus that accumulate during experimental anti-GBM GN in rat.
Macrophage depletion has been proven to be a valuable tool in evaluating the contribution of the macrophage to the development of pathological conditions. Clodronate, a bisphosphonate has little effect on the viability of the macrophage in the free form, but encapsulated into liposomes or MS (as in this study) there was a transient depletion of the macrophage population within 24-48 hours. The depletion of macrophages by clodronate liposomes was shown to be caused by apoptosis-induced cell death. We speculate a similar mechanism of action for clodronate MS.
The reduction in endotoxin-induced TNF-alpha and IL-1-beta release after pretreatment with clodronate MS as seen in this study has also been shown by others using clodronate liposomes. It has also been shown that clodronate liposomes can attenuate cytokine gene expression in mice. In the whole blood model, we also demonstrated a greater reduction of endotoxin-induced cytokine release with clodronate MS when compared to clodronate in free form. There was nearly a complete inhibition of both TNF-alpha and IL-1-beta release at the highest dose of clodronate MS that contained, not greater than 100 μg of free clodronate. The mechanism of action of clodronate MS is likely due to phagocytosis of the albumin MS containing clodronate in a similar fashion to liposomes followed by the release of the clodronate intracellularly that produces an inhibition of cytokine release due to death of macrophages. Inhibition of cytokine release by clodronate may be beneficial in the treatment of disease states characterized by proinflammatory cytokine release.
Previous studies have shown that macrophages have an important role in induction and progression of renal damage in GN. One of the hallmarks of GN is proteinuria and macrophage infiltration. The reduction in macrophage infiltration by clodronate MS in experimental GN has been previously shown by our group. We have shown that the anti-GBM induced GN causes macrophage infiltration (8.2 cells/glomerular cross-section) and treatment with clodronate MS prevented macrophage infiltration (2.2 cells/glomerular cross-section) similar to that seen in this study. In addition, we have also shown that anti-GBM GN-induced proteinuria (43 mg/24 hr) can also be significantly reduced with clodronate MS (8.4 mg/24 hr) to the same level found in normal healthy rats (5.3 mg/24 hr). Clodronate MS may be therapeutically beneficial by depleting macrophages in GN.
Effect of clodronate on endotoxin-induced TNF-alpha and IL-1-beta release is shown in
Tissue sections stained for ED1 positive macrophages demonstrate that was a significant (p<0.001) reduction of ED1 positive macrophages from liver and spleen of rats that received clodronate MS compared to healthy control rats (see Table 3).
aPercentage of the total leucocytes;
There was also a significant reduction in circulating monocytes in peripheral blood (Table 3, p<0.001). Similarly, kidney sections stained for ED1 positive macrophages show that there was no macrophage infiltration into the glomerulus of normal healthy kidneys and induction of anti-GBM GN caused ED1 positive macrophage infiltration. Pretreatment with clodronate MS significantly reduced the macrophage infiltration in anti-GBM GN.
In conclusion, these studies demonstrate that albumin MS containing clodronate is an effective tool for total body depletion of macrophages in the rat. Depletion of macrophages by clodronate MS produced attenuation of pro-inflammatory cytokines and amelioration of experimental anti-glomerular basement membrane GN that has been demonstrated to be macrophage-dependent. Transient depletion of macrophages may be a treatment modality for macrophage-dependent disease state.
To each ml of blood 25, 50 and 100 μg of free clodronate in saline or 50, 100 and 200 μg of clodronate MS (equivalent to 25, 50 and 100 μg of free clodronate respectively) in saline was added. In all groups, the saline group received 50 μl of saline and blank MS group received 400 μg of blank MS for each ml of blood. Two hour later 100 ng/ml of endotoxin was added and the blood was incubated for 24 hours in an atmosphere of 5% CO2 at 37 degrees C. Plasma levels after endotoxin challenge is shown in this figure. The MS form of CLON attenuated endotoxin-induced TNF-alpha levels significantly better than the free form of CLON at p<0.05 level.
Bioactive Protein Drug NF-KB
Application-Septic Shock
Method of Preparation-Emulsification Method
Preparation of Microspheres Containing Cytokine Antagonist Namely Anti-Sense Oligomers to NF-KB (Bio-Active Protein Drug)
Evaluation in Whole Blood Model, Endotoxic Shock Model and Peritonitis Model
Microencapsulated Antisense Oligomers to NF-Kb; a New Approach to Pro-Inflammatory Cytokine Inhibition
A) Introduction
Inhibition of individual protein synthesis is possible by antisense oligonucleotides after binding with its specific mRNA. However, inadequate intracellular penetration of antisense compounds has limited their effectiveness. Antisense compounds contained within microencapsulated albumin takes advantage of the normal phagocytic function of macrophages to deliver antisense oligonucleotides intracellularly for improved exposure of the oligomers to nuclear and cytosolic mRNA. Flourescein labeled oligonucleotides when microinjected into macrophages appears in the nucleus within minutes, thus interacting immediately with synthesized mRNA.
Studies done in our laboratory have demonstrated that albumin microcapsules 1) are rapidly phagocytozed by macrophages in-vitro and in-vivo 2) are distributed to over 90% of monocytes/macrophages in the liver, spleen, kidney and blood and 3) migrate to the area of infection. In previous studies, we have demonstrated improved efficacy of micro encapsulated neutralizing antibodies to TNF and IL1 in both in-vitro cytokine suppression and animal survival using an in-vivo fatal endotoxic shock model and a peritonitis model of infection. Thus, microencapsulated drug delivery directly targeting the macrophage, which secretes the majority of proinflammatory cytokines, may improve the efficiency of these compounds.
NF-kB has recently been described and is thought to be the nuclear transcription factor responsible for the synthesis of proinflammatory cytokines such as TNF and IL1. Other substances involved in the inflammatory process are also regulated by NF-kB. Increased activity of NF-kB has been described in sepsis and in other inflammatory conditions such as glomerulonephritis, acute respiratory distress syndrome, and inflammatory bowel disease. Thus, antisense oligonucleotides to NF-kB may alter the inflammatory response by suppressing the synthesis of the proinflammatory cytokines. Microencapsulation of these compounds may further improve efficiency by direct macrophage targeting.
The aims of the present study are as follows:
a) to determine if albumin microencapsulation of antisense oligomers to NF-kB will improve suppression of TNF, IL1, IL6 and IL8 to endotoxin stimulation in an in-vitro whole blood model and
b) to determine if microencapsulated oligomers to NF-kB will suppress proinflammatory cytokines and improve survival using in-vivo endotoxic shock and peritonitis models.
B) Preparation of Microspheres.
The microencapsulated anti-sense oligonucleotides to NF-kB were made according to Example 1.
C) Experimental Methods
Samples of blood were drawn from normal human volunteers and separated into multiple 1 ml aliquots. 100 ug of E. Coli endotoxin was added to each specimen. Cytokine levels were determined by ELISA in duplicate in each group after the following incubation times: TNF—4 hours, IL1—24 hrs.
The following groups were studied:
1. control: endotoxin+saline
2. NF-kB antisense in solution, 200 and 300 ug/ml given 1 hr prior to the addition of endotoxin
3. NF-kB non-sense (scrambled) 200 and 300 ug/ml
4. Microencapsulated antisense oligomers to NF-kB 200 and 300 ug/ml
5. Microencapsulated non-sense (scrambled) oligomers 200 and 300 ug/ml
Endotoxic shock was produced in Fischer rats weighing approximately 150 grams by intravenous injection of 15 mg/kg of E. Coli endotoxin. TNF was measured by ELISA at 0, 4 hrs, 8 hrs, 24 hrs and 48 hrs. Survival was observed for 5 days (120 hrs).
After a dose response study was performed, 300 ug of microencapsulated antisense oligomers to NF-kB was injected into 10 rats and 300 ug of oligomer in solution were given intravenously to 10 rats.
Peritonitis was induced in rats by the intraperitoneal injection of 1010 organisms of E. Coli. gentamycin 15 mg/kg was given intraperitoneally for 3 consecutive days. TNF was measured at 0 hrs, 4 hrs, 8 hrs, 24 hrs, and 48 hrs. Survival was observed for 5 days (120 hrs).
1. Simultaneous treatment: E. Coli peritoneal injection and the following treatments were given simultaneously and then daily for an additional 2 days.
a. control
b. microencapsulated NF-kB I.V. 400 ug/rat n=10
c. microencapsulated NF-kB I.V. 200 ug/rat n=10
d. solution NF-kB I.V. 400 ug/rat n=10
e. solution NF-kB I.V. 200 ug/rat n=10
2. Delayed treatment: Treatment with the above doses of oligomer initially given 4 hrs after the dose of intra peritoneal E. Coli (at the peak TNF level) and then for an additional 2 days.
D) Results and Discussions:
Microencapsulation of antisense oligomers to NF-kB improves pro-inflammatory cytokine inhibition by increased intracellular penetration into the macrophage. Microencapsulated antisense oligomers to NF-kB inhibit TNF>IL1>IL6>IL8 to a greater extent than equivalent amounts of oligomer in solution (p<0.05) using the in-vitro whole blood model. Microencapsulated NF-kB oligomers produced a dose dependent improvement in TNF inhibition in the endotoxic shock model in rats. 80% survival at a dose of 300 ug per rat was observed compared to 20% in the endotoxic shock model with an equivalent dose in solution (p<0.05). Microencapsulated oligomers produced 80% survival in the peritonitis model and 70% survival in the delayed treatment group compared to 30 and 20% in the solution group respectively. TNF and IL1 were inhibited to a greater extent in the microencapsulated group. Survival occurred in the delayed treatment group with microencapsulated oligomers even when given after the peak in TNF occurred.
In summary, microencapsulated oligomers to NF-kB improve pro-inflammatory cytokine inhibition both in-vitro and in-vivo with improved mortality in otherwise fatal models of endotoxic shock and peritonitis. Microencapsulated oligomers to NF-kB may be of value in the treatment of pathological conditions characterized by pro-inflammatory cytokine activation.
E) Results:
A) Introduction:
We were interested in evaluating microspheres prepared by a nebulization method of different categories of drug types (bio-active proteins, oligonucleotides, chemicals, vaccines) and also to study the effect of variations in oils, temperature and methodologies on the preparation of microspheres. We used a biodegradable non-antigenic albumin matrix to microencapsulate the cytokine antagonists [such as anti-sense oligomers to NF-kB].
B) Experimental Methodology
Microsphere Preparation:
Nebulization Method:
General Methodology:
The general basis of this invention involves the following steps:
An aqueous solution of the drug (which may be a bioactive protein, drug or a synthetic drug) to be microencapsulated is prepared along with the encapsulating polymer (such as, but not limited to, albumin, chitosan, globulin or some other bio-degradable natural or synthetic polymer). The polymer-drug solution is then aerosolized (with the aid of some spray forming device, such as, but not limited to, an ultrasonic nebulizer) to form a fine mist-like spray. This mist or spray containing the polymer-drug (or other material) solution is then directed into a solvent system such as butanol or other lower carbon alcohol, such as, but not limited to methanol, ethanol, propanol, and the like (see
Some of the advantages of this method are as follows:
Bioactive Protein Drug NF-KB
Application-Septic Shock
Method of Preparation-Nebulization
Preparation of Microspheres Containing Cytokine Antagonist Namely Anti-Sense Oligomers to NF-KB (Bio-Active Protein Drug) by the Nebulization Method
A) Introduction.
Microspheres containing the cytokine antagonist [(anti-sense oligomer to NF-kB (bio-active protein drug) were evaluated in this study.
B) Preparation of the anti-sense oligonucleotides to NF-kB by albumin using the nebulization method.
Microspheres containing the cytokine antagonist [(anti-sense oligomer to NF-kB (bio-active protein drug)] were cross-linked to the albumin microsphere matrix.
In all cases the microspheres were suspended in pyrogen free water or saline before use. In the nebulization step, the particles created at the spray head were conducted via a tube to the container containing the solvent in step 5) above and the tube tip was maintained below the surface of the solvent so that the nebulized particles were introduced into the solvent solution below the air interface surface so as to minimize loss to the atmosphere.
The above procedure was repeated in order to evaluate to use of different types of oils and solvent systems as the emulsifying media, and different temperatures on manufacture were also evaluated in addition to the 5 degree C. described above. Finally, in addition to water, different solvents were also evaluated as the media for dissolution of the drug. The following variations were evaluated:
Different oils/solvents such as olive oil, cottonseed oil, canola oil, mineral oil and butanol were used for the study.
The microspheres were prepared under wide variations of temperature conditions.
In addition to PBS, saline, distilled/de-ionized water and water with Tween® 80 were used to dissolve the albumin and the drug.
The effect of cross-linking was evaluated where the cross-linking agent is added after all the microspheres are atomized into the solvent.
C) Experimental Methodology:
Drug content analysis was determined by HPLC methods developed in our laboratory.
The preparations were evaluated for drug efficacy with the aid of the whole blood model, briefly outlined as follows: Blood was pooled into lavender top tubes containing EDTA. The blood was separated into three 5 ml aliquots and pre-treated for 1 hour with one of the following batches of microspheres and challenged with endotoxin (100 mcg/ml). Samples were obtained at 0 and 4 hours post endotoxin challenge to determine the TNF-alpha levels.
D) Results:
Chemical Drug Pyrrolidine Dithiocarbamate
Application-Septic Shock
Method of Preparation-Emulsification
Preparation and Evaluation of Microencapsulated
Pyrrolidine Dithiocarbamate
A) Introduction: Pyrrolidine dithiocarbamate (PTDC) is a water soluble, low molecular weight antioxidant substance, which inhibits NF-kB activation. NF-kB is the nuclear transcription factor, which is responsible for the activation of pro-inflammatory cytokines. Several studies have demonstrated the effectiveness of PTDC in cytokine inhibition in-vitro as well as improving mortality in endotoxic shock models in rats. We have demonstrated the improvement of the efficiency of compounds such as neutralizing antibodies and antisense oligomers to NF-kB in cytokine inhibition both in-vitro and in-vivo. Microencapsulation of a compound targets the macrophage and improves the efficiency of cytokine inhibition.
The whole blood model will be used to evaluate the efficacy of the microencapsulated PDTC. Three doses [15 micromoles (uM), 30 uM, and 60 uM] will be studies studied. These doses will be added to 1 ml aliquots in both encapsulated and solution form. TNF alpha will be measured by the standard ELISA procedure.
Although only a few exemplary embodiments of this invention have been described in detail above, those skilled in the art will readily appreciate that many modifications are possible in the exemplary embodiments without materially departing from the novel teachings and advantages of this invention. Accordingly, all such modifications are intended to be included within the scope of this invention as defined in the following claims. It should further be noted that any patents, applications and publications referred to herein are incorporated by reference in their entirety.
This application is a continuation-in-part of application U.S. application Ser. No. 08/434,542, filed May 4, 1995, now U.S. Pat. No. 6,555,110 , which is a continuation-in-part of application Ser. No. 07/977,057, filed Nov. 16, 1992 (now abandoned), all of which are commonly assigned to the assignee of the present application. The disclosures of all these applications are incorporated by reference in their entirety herein.
| Number | Name | Date | Kind |
|---|---|---|---|
| 3137631 | Soloway | Jun 1964 | A |
| 3429827 | Ruus | Feb 1969 | A |
| 3663685 | Evans | May 1972 | A |
| 3663686 | Grotenhuis | May 1972 | A |
| 3663687 | Evans | May 1972 | A |
| 3758678 | Lindsey et al. | Sep 1973 | A |
| 3937668 | Zolle | Feb 1976 | A |
| 3962414 | Michaels | Jun 1976 | A |
| 4147767 | Yapel, Jr. | Apr 1979 | A |
| 4169804 | Yapel, Jr. | Oct 1979 | A |
| 4186183 | Steck et al. | Jan 1980 | A |
| 4230687 | Sair et al. | Oct 1980 | A |
| 4349530 | Royer | Sep 1982 | A |
| 4356259 | Banba | Oct 1982 | A |
| 4671954 | Goldberg et al. | Jun 1987 | A |
| 4674480 | Lemelson | Jun 1987 | A |
| 4680174 | Jarvis, Jr. et al. | Jul 1987 | A |
| 4764359 | Lemelson | Aug 1988 | A |
| 4925661 | Huang | May 1990 | A |
| 4963367 | Ecanow | Oct 1990 | A |
| 5017379 | Lemelson | May 1991 | A |
| 5069936 | Yen | Dec 1991 | A |
| 5129877 | Gallo et al. | Jul 1992 | A |
| 5690954 | Illum | Nov 1997 | A |
| 3202731 | Grevenstuk et al. | Sep 2003 | A1 |
| 20020177568 | Stinchcomb et al. | Nov 2002 | A1 |
| 20040043079 | D'Souza | Mar 2004 | A1 |
| 20050089576 | Moreau | Apr 2005 | A1 |
| Number | Date | Country |
|---|---|---|
| WO 9410980 | May 1994 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 20040043079 A1 | Mar 2004 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 08434542 | May 1995 | US |
| Child | 10231791 | US | |
| Parent | 07977057 | Nov 1992 | US |
| Child | 08434542 | US |
