Patent Application
20230295199
The present invention relates to phospholipids and the like.
In recent years, pharmaceuticals containing small interfering RNA (siRNA) and genetic vaccines containing messenger RNA (mRNA) have been under development. An extremely sophisticated delivery system is required for externally administered RNA to exhibit its intrinsic activity in vivo. This is because RNA is readily degraded by nucleases, and poorly penetrates cell membranes. Thus, the commercial viability of RNA-containing pharmaceuticals and vaccines inevitably involves the development of a delivery system.
A known delivery system for medicinal substances, such as RNA, is administration of a medicinal substance encapsulated a lipid particle. However, administering a negatively charged nucleic acid typically involves the use of a positively charged lipid to cause electrostatic interaction; this raises concerns regarding cytotoxicity.
PTL 1 has reported that a charge-reversible phospholipid has siRNA encapsulation properties and safety at a physiological pH.
PTL 1: WO2018/190017
A phospholipid alcohol solution is generally used in the production of lipid particles. When preparing an alcohol solution of the phospholipid of PTL 1, it was necessary to use t-butanol to dissolve the phospholipid. However, t-butanol has a melting point near room temperature and may solidify depending on the operating temperature. The present inventors considered ethanol desirable because it does not solidify near room temperature and is recognized as an additive for medical drugs.
An object of the present invention is to provide a charge-reversible and ethanol-soluble phospholipid suitable for the preparation of lipid particles.
The present inventors conducted extensive research to achieve the above object, and found that the object can be achieved by a phospholipid represented by formula (1). Upon further research based on this finding, the present inventors have completed the present invention. Specifically, the present invention includes the following embodiments.
Item 1. A phospholipid represented by formula (1):
wherein R1 and R2 are the same or different and each represent a chain hydrocarbon group, R3 represents a hydrogen atom or a hydrocarbon group, and m represents an integer of 1 to 3.
Item 2. The phospholipid according to Item 1, wherein the chain hydrocarbon group is an unsaturated chain hydrocarbon group.
Item 3. The phospholipid according to item 1 or 2, wherein the chain hydrocarbon group has 11 to 23 carbon atoms.
Item 4. The phospholipid according to any one of Items 1 to 4, wherein in m is 2.
Item 5. The phospholipid according to any one of Items 1 to 4, wherein R3 is a hydrogen atom or an alkyl group.
Item 6. A lipid particle comprising the phospholipid according to any one of Items 1 to 5 (phospholipid A).
Item 7 The lipid particle according to Item 6, in which a medicinal substance encapsulated.
Item 8. The lipid particle according to Item 7 wherein the medicinal substance is a polynucleotide.
Item 9. The lipid particle according to any one of Items 6 to 8, comprising a sterol.
Item 10. The lipid particle according to any one of Items 6 to 9, wherein phospholipid A has an unsaturated chain hydrocarbon group, and the lipid particle further comprises a phospholipid other than phospholipid A (phospholipid B).
Item 11. An alcohol solution comprising the phospholipid according to any one of Items 1 to 5.
Item 12. The alcohol solution according to Item 11, wherein the alcohol is ethanol.
Item 13. A method for producing a lipid particle, the method comprising mixing the alcohol solution according to Item 11 or 12 with an acidic aqueous solution.
Item 14. A medical drug comprising the lipid particle according to any one of Items 6 to 10.
The present invention can provide a charge-reversible and ethanol-soluble phospholipid suitable for the preparation of lipid particles.
In this specification the, terms “comprise,” “contain,” and “include” include the, concepts of “comprise, ” “contain,” “include,” “consist essentially of,” and “consist of.”
The present invention, according to one embodiment thereof, relates to a phospholipid represented by formula (1):
wherein R1 and R2 are the same or different and each represent a chain. hydrocarbon group, R3 represents a hydrogen atom or a hydrocarbon group, and m represents an integer of 1 to 3 (which may be referred to as “the phospholipid of the present invention” in this specification). The following describes this phospholipid.
The chain hydrocarbon group represented by R1 or R2 is not particularly limited as long as it is a monovalent hydrocarbon group, and may be a linear or branched (preferably linear) hydrocarbon group. The number of carbon atoms in the chain hydrocarbon group is not particularly limited, as long as it is a number that allows the formation of lipid particles. For example, the number of carbon atom is 3 to 29, preferably 7 to 25, more preferably 11 to 21, still more preferably 13 to 19, and still yet more preferably 14 to 18. The chain hydrocarbon group may be a saturated or unsaturated hydrocarbon group, but is preferably an unsaturated chain hydrocarbon group, more preferably an unsaturated chain hydrocarbon group containing a double bond, and still more preferably an unsaturated chain hydrocarbon group containing only one double bond. Examples of the chain hydrocarbon group include propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, tridecyl, tetradecyl, pentadecyl, 9-pentadecenyl, hexadecyl, heptadecyl, cis-9-heptadecenyl, 11-heptadecenyl, cis,cis-9,12-heptadecadienyl, 9,12,15-heptadecatrienyl, 6,9,12-heptadecatrienyl, 9,11,13-heptadecatrienyl, nonadecyl, 8,11-nonadecadienyl, 5,8,11-nonadecatrienyl, 5,8,11,14-nonadecatetraenyl, henicosyl, trichosyl, cis-15-tricosenyl, pentacosyl, heptacosyl, and nonacosyl.
It is preferable that at least one of R1 and R2 is an unsaturated chain hydrocarbon group, and it is more preferable that both of them are unsaturated chain hydrocarbon groups.
The hydrocarbon group represented by R3 is not particularly limited, as long as it is a monovalent hydrocarbon group. The hydrocarbon group is preferably a chain hydrocarbon group, and more preferably an alkyl group. The number of carbon atoms in the hydrocarbon group is not particularly limited, and is, for example, 1 to 8, preferably 1 to 6, more preferably 1 to 4, still more preferably 1 or 2, and particularly preferably 1.
R3 is preferably a hydrogen atom or an alkyl group, and more preferably a hydrogen atom.
m is preferably 2.
The phospholipid of formula (1) also includes salt forms. The salt can be an acidic salt or a basic salt. Examples of acidic salts include inorganic acid salts, such as hydrochloride, hydrobromide, sulfate, nitrate, and phosphate; and organic acids, such as acetate, propionate, tartrate, fumarate, maleate, malate, citrate, methanesulfonate, and para-toluenesulfonate. Examples of basic salts include alkali metal salts, such as sodium salts and potassium salts; alkaline earth metal salts, such as calcium salts and magnesium salts; salts with ammonia; and salts with organic amines, such as morpholine, piperidine, pyrrolidine, monoalkylamine, dialkylamine, trialkylamine, mono(hydroxyalkyl)amine, di(hydroxyalkyl)amine, and tri(hydroxyalkyl)amine.
The phospholipid of the present invention can be synthesized by various methods. The compound of the present invention can be synthesized, for example, in accordance with or with reference to the following reaction scheme:
wherein R1, R2, R3, and m are as defined above.
In this reaction, the compound represented by formula (A) is reacted with the compound represented by formula (B) in the presence of phospholipase D, thereby preparing the compound represented by formula (1).
From the standpoint of yield etc., the amount of the compound represented by formula (B) for use is preferably 3 to 25 mol, and more preferably 8 to 18 mol, per mol of the compound represented by formula (A).
From the standpoint of yield etc., the amount of phospholipase D for use is preferably 50 to 1000 U, and more preferably 200 to 500 U, per mol of the compound represented by formula (A). 1 U is defined as an enzyme amount with which 1 micro-mol (μmol) of a substrate is changed per minute (1 micro-mol per minute) under optimum conditions (an acidity at which the chemical reaction proceeds most at a temperature of 30° C.)
This reaction is performed in the presence of a solvent. The solvent is not particularly limited, as long as the solvent can help phospholipase D exert its activity. The solvent preferable for use includes various buffers. A preferable buffer is an acetate buffer. The solvent preferably has a pH of 4 to 7, and more preferably 5 to 6. This reaction system may contain various organic solvents for dissolving the compound represented by formula (A) (e.g., ethyl acetate), in addition to the aqueous solvent.
This reaction is typically performed by mixing a solution of the compound represented by formula (A) in an organic solvent with a solution of the compound represented by formula (B) in an aqueous solvent, and adding phospholipase U to the mixture.
In this reaction, additives, in addition to the components described above, may also be suitably used to the degree that the progress of the reaction is not significantly interfered with.
The reaction temperature is not particularly limited, as long as the temperature allows phospholipase D to exert its activity. The reaction temperature is typically 20 to 50° C., and preferably 35 to 45° C.
The reaction time is not particular limited, as long as the reaction time allows phospholipase D to exert its activity. The reaction time is typically 6 hours to 72 hours, and preferably 12 hours to 24 hours.
After completion of the reaction, the solvents are evaporated off, and the product can be isolated and purified by typical techniques, such as chromatography and recrystallization. The structure of the product can be identified, for example, by element analysis, MS (FD-MS) analysis, IR analysis, 1H-NMR, or 13C-NMR.
To improve lipid nanoparticie safety, ionizable lipids have been developed and nanoparticulated. Ionizable lipids are positively charged in the acidic range, and the change in net electrical charge in that case is 0→+1. However, the change in net electrical charge of the phospholipid of the present invention (charge-reversible lipid) can be within the range of −1 to +2; the viewpoint is different. The phospholipid of the present invention is even ionized under neutral conditions, and differs from ionizable lipids in physicochemical properties. Because the lipid of the present invention is able to behave as an amphipathic lipid under neutral conditions, the lipid can offer the prospect of higher stability and higher safety.
The use of the phospholipid of the present invention enables the formation of a lipid particle that is not positively charged at a pH of the body fluid (typically in the neutral range), and that enables efficient onset of the effect of a medicinal substance encapsulated in the lipid particle.
The present invention, according to one embodiment thereof, relates to a lipid particle (in this specification, “the lipid particle of the present invention”) containing the phospholipid of the present invention (in this specification, “phospholipid A”). The following describes this particle.
The lipid particle of the present invention is not particularly limited, as long as it contains the phospholipid of the present invention as a component lipid of the particle. The phospholipid of the present invention contained in the lipid particle may be one type alone, or a combination of two or more types. The lipid particle of the present invention is, for example, formed such that an amphipathic lipid containing the phospholipid of the present invention forms the outer layer, and the lipid molecules are lined with their hydrophilic portions facing outward. Examples of the lipid particle include particles having the outer layer formed from a lipid monolayer membrane, and particles having the outer layer formed from a lipid bilayer membrane. The lipid particle is preferably a particle having the outer layer formed from a lipid monolayer membrane, and more preferably a particle having the outer layer formed from a lipid monolayer membrane in which amphipathic lipid molecules are lined with their hydrophilic portions facing outward. The inner layer of the particle may be composed of a homogeneous aqueous phase or a homogeneous oil phase, and the inner layer preferably contains one or multiple reverse micelles.
The particle size of the lipid particle of the present invention is not particularly limited. The particle size is preferably nanosize, and is specifically, for example, 10 to 700 nm, preferably 20 to 500 nm, more preferably 40 to 200 nm, and still more preferably 60 to 150 nm.
The lipid particle of the present invention is not positively charged at a pH of the body fluid (typically in the neutral range). More specifically, the lipid particle of the present invention has a zeta potential of −80 to −1 mV, −60 to −10 mV, or −60 to −20 mV in a buffer with a pH of 7.0.
The lipid particle of the present invention may contain other lipids as a lipid component of the particle, in addition to the phospholipid of the present invention. Specific examples of such lipids include phospholipids, glycolipids, sterols, and saturated or unsaturated fatty acids.
Specific examples of phospholipids include phosphatidylcholines, such as dilauroylphosphatidylcholine, dimyristoylphosphatidylcholine, dipalmitoylphosphatidylcholine, distearoylphosphatidylcholine, dioleoylphosphatidylcholine, dilinoleoylphosphatidylcholine, myristoylpalmitoylphosphatidylcholine, myristoylstearoylphosphatidylcholine, and palmitoylstearoylphosphatidylcholine; phosphatidylglycerols, such as dilauroylphosphatidylglycerol, dimyristoylphosphatidylglycerol, dipalmitoylphosphatidylglycerol, distearoylphosphatidylglycerol, dioleoylphosphatidylglycerol, dilinoleoylphosphatidylglycerol, myristoylpalmitoylphosphatidylglycerol, myristoylstearoylphosphatidyldlycerol, and palmitoylstearoylphosphatidylglycerol; phosphatidylethanolamines, such as dilauroylphosphatidylethanolamine, dimyristoylphosphatidylethanolamine, dipalmitoylphosphatidylethanolamine, distearoylphosphatidylethanolamine, dioleoylphosphatidylethanolamine, dilinoleoylphosphatidylethanolamine, myristoylpalmitoylphosphatidylethanolamine, myristoylstearoylphosphatidylethanolamine, and palmitoylstearoylphosphatidylethanolamine; phosphatidylserine; phosphatidic acid; phosphatidylinositol; sphingomyelin; cardiolipin; egg yolk lecithin; soybean lecithin; and hydrogenated products thereof. These phospholipids may be those modified with a water-soluble polymer, such as PEG.
Specific examples of glycolipids include glyceroglycolipids, such as diglycosyl diglyceride, digalactosyl diglyceride, galactosyl diglyceride, and glycosyl diglyceride; glycosphingolipids, such as galactosyl cerebroside and ganglioside; and stearyl glucoside and esterified stearyl glycoside.
Specific examples of sterols include cholesterol, cholesteryl hemisuccinate, lanosterol, dihydrolanosterol, desmosterol, dihydrocholesterol, phytosterol, phytosterol, stigmasterol, timosterol, ergosterol, sitosterol, campesterol, and brassicasterol. The lipid particle preferably contains a sterol as a lipid component of the liposome membrane, particularly because of its action to stabilize the liposome membrane, and to adjust the fluidity of the liposome membrane.
Specific examples of saturated or unsaturated fatty acids include saturated or unsaturated fatty acids having 10 to 22 carbon atoms, such as decanoic acid, myristic acid, palmitis acid, stearic acid, arachidonic acid, oleic acid, and docosanoic acid.
These lipids may be used singly, or in a combination of two or more.
The lipid particle of the present invention preferably contains a phospholipid other than the phospholipid of the present invention (in this specification, “phospholipid B”), and/or a sterol, and more preferably phospholipid X and a sterol. According to one embodiment of the present invention, when the phospholipid of the present invention has an unsaturated chain hydrocarbon group, phospholipid B preferably has a saturated chain hydrocarbon group. Phospholipid B is preferably phosphatidylcholine, and particularly preferably dipalmitoyl phosphatidylcholine. Other examples of phospholipid B include distearoylphosphatidylcholine, dimyristoylphosphatidylcholine, dioleoylphosphatidylcholine, palmitoyloleoylphosphatidylcholine, and the like. The sterol is preferably cholesterol
When the lipid particle of the present invention contains phospholipid B, phospholipid B is present in an amount of, for example, 15 to 100 mol, preferably 30 to 70 mol, more preferably 40 to 60 mol, and still more preferably 45 to 55 mol, per 100mol of the phospholipid of the present invention. Alternatively, phospholipid B is present in an amount of, for example, 5 to 70 mol, preferably 10 to 40 mol, more preferably 15 to 30 mol, and still more preferably 17 to 27 mol, per 100 mol of the phospholipid of the present invention.
When the lipid particle of the present invention contains a sterol, the sterol is present in an amount of, for example, 30 to 200 mol, preferably 60 to 140 mol, more preferably 80 to 120 mol, still more preferably 90 to 110 mol, and still yet more preferably 95 to 105 mol, per 100 mol of the phospholipid of the present invention.
When the lipid particle of the present invention contains phospholipid B and a sterol, phospholipid B is present in an amount of, for example, 15 to 100 mol, preferably 30 to 70 mol, more preferably 40 to 60 mol, and still more preferably 45 to 55 mol, per 100 mol of the sterol. Alternatively, phospholipid B is present in an amount of, for example, 5 to 70 mol, preferably 10 to 40 mol, more preferably 15 to 30 mol, and still more preferably 17 to 27 mol, per 100 mol of the sterol.
The phospholipid of the present invention and optionally added other lipids (in a preferable embodiment, phospholipid B and a sterol) are present in a total amount of, for example, 50 mol % or more, preferably 70 mol % or more, more preferably 90 mol % or more, still more preferably 95 mol % or more, and still yet more preferably 99 mol % or more, per 100 mol % of the lipid component of the lipid particle of the present invention.
In the lipid particle of present invention, part of the phospholipid can be modified with a water-soluble polymer, such as PEG. A phospholipid modified with PEG is present in an amount of, for example, 0 to 50 mol %, preferably 0 to 30 mol %, more preferably 0 to 20 mol %, and still more preferably 0 to 15 mol %, per 100 mol % of the lipid component of the lipid particle of the present invention.
In the lipid particle of the present invention, a medicinal substance is preferably encapsulated. The medicinal substance is not particularly limited, and examples include polynucleotides, peptides, proteins, carbohydrates, and low-molecular compounds. The medicinal substance is preferably negatively charged, and preferably water-soluble. Such a medicinal substance suitably usable is a polynucleotide. The target disease of the medicinal substance is not particularly limited, and examples include cancer (in particular, solid cancer).
The polynucleotide is not particularly limited, as long as the polynucleotide can function as a medicinal substance. Examples include siRNA, miRNA, antisense nucleic acids, expression vectors therefor, expression vectors for proteins, nucleic acids for genome editing (e.g., guide RNAs, Cas protein expression vectors, and TALEN expression vectors), and nucleic acid vaccines.
The polynucleotide may have a known chemical modification as descried below. To prevent degradation by hydrolases such as nucleases, the phosphoric residue (phosphate) of each nucleotide may be replaced with a chemically modified phosphoric residue, such as phosphorothioate (PS), methylphosphonate, or phosphorodithionate. The hydroxyl group at position 2 of the sugar (ribose) of each ribonucleotide may be replaced with —OR (R represents, for example, CH3(2′-O-Me), CH2CH2OCH3(2′-O-MOE), CH2CH2NHC(NH)NH2, CH2CONHCH3, or CH2CH2CN). Additionally, the base moiety pyrimidine, purine) may be chemically modified; for example, introduction of a methyl group or a cationic functional group into position 5 of the pyrimidine base, or replacement of the carbonyl group at position 2 into thiocarbonyl. The phosphoric moiety or hydroxyl moiety may also be modified with, for example, a biotin, an amino group, a lower alkyl amine group, or an acetyl group. However, chemical modification is not limited thereto. Additionally, BNA (LNA), for example, whose sugar moiety conformation is immobilized in N form by bridging the 2′ oxygen and 4′ carbon in the sugar moiety of the nucleotide, can also be preferably used.
The medicinal substance is preferably contained in the inner layer of the lipid particle of the present invention. When the medicinal substance is a polynucleotide, the medicinal substance is preferably contained within a reverse micelle in the inner layer.
The molar ratio of the lipid component of the lipid particle of the present invention to the medicinal substance (the lipid component of the lipid particle of the present invention/the medicinal substance, mol/mol) is, for example, 500 or more, preferably 1000 or more, more preferably 1500 or more, still more preferably 1900 or more, still yet more preferably 2500 or more, and particularly preferably 3200 or more, when, for example, the medicinal substance is a polynucleotide, such as siRNA. The upper limit of the molar ratio is not particularly limited, and is, for example, 10000, 7000, or 5000.
The lipid particle of the present invention may contain other components in addition to the components described above. Examples of other components include membrane stabilizers, charged substances, antioxidants, membrane proteins, polyethylene glycol (PEG), antibodies, peptides, and sugar chains.
An antioxidant can be added to prevent oxidation of the membrane, and is optionally used as a component of a membrane. Examples of antioxidants used as a component of a membrane include butylated hydroxytoluene, propyl gallate, tocopherol, tocopheryl acetate, mixed tocopherol concentrate, vitamin E, ascorbic acid, L-ascorbyl stearate, ascorbyl palmitate, sodium hydrogen sulfite, sodium sulfite, sodium edetate, erythorbic acid, and citric acid.
A membrane protein can be added to add functions to a membrane, or to stabilize the, structure of a membrane, and is optionally used as a component of a membrane. Examples of membrane proteins include peripheral membrane proteins, integral membrane proteins, albumin, and recombinant albumins.
The other components are present in an amount of, for example, 10% or less, preferably 5% or less, more preferably 2% or less, and still more preferably 1% or less, based on 100 mass % of the lipid particle of the present invention.
The lipid particle of the present invention can be produced in accordance with or with reference to a known production method for a lipid particle. The lipid particle of the present invention can be produced preferably by a method including the step of mixing a alcohol solution containing the phospholipid of the present invention with an acidic aqueous solution (step 1).
The alcohol as a solvent of the alcohol solution is not particularly limited, as long as the alcohol can dissolve the phospholipid. From the standpoint of solubility, the alcohol is preferably ethanol, 2-propanol, t-butanol, or the like. Of these, ethanol is particularly preferably used, from the standpoint of easy handling, safety, etc.
The acidic aqueous solution typically contains an acid in addition to water, which is a solvent. Examples of the acid include organic acids and inorganic acids, with organic acids being preferable. Examples of organic acids include maleic acid, formic acid, acetic acid, propionic acid, folic acid, isobutyric acid, valeric acid, isovaleric acid, pyruvic acid, oxalic acid, malonic acid, succinic acid, glutaric acid, ketoglutaric acid, adipic acid, lactic acid, tartaric acid, fumaric acid, oxaloacetic acid, malic acid, isocitric acid, citric acid, benzoic acid, phthalic acid, isophthalic acid, terephthalic acid, hemimellitic acid, trimellitic acid, trimesic acid, mellophanic acid, prehnitic acid, pyromellitic acid, mellitic acid, methanesulfonic acid, benzenesulfonic acid, p-toluenesulfinic acid, camphorsulfonic acid, p-toluenesuifinic acid, and benzenesulfinic acid; with citric acid being preferable. Examples of inorganic acids include hydrochloric acid, sulfuric acid, nitric acid, carbonic acid, boric acid, boronic acid, hydrofluoric acid, hypochlorous acid, chlorous acid, chloric acid, perchloric acid, hypobromous acid, bromous acid, bromic acid, perbromic acid, hypoiodous acid, iodous acid, iodic acid, periodic acid, phosphorus acid, phosphoric acid, polyphosphoric acid, chromic acid, permanganic acid, and Amberlyst. The acids may be used singly, or in a combination of two or more.
The acidic aqueous solution preferably has a pH of 3 to 5.
The acidic aqueous solution preferably contains a water-soluble medicinal substance.
The mixture ratio, of the acidic aqueous solution to the alcohol solution (the acidic aqueous solution/the alcohol solution, v/v) is, for example, 1.5 to 10, preferably 2 to 8, and more preferably 3 to 6.
Mixing is not particularly limited, as long as the mixing mode allows the phospholipid to be mixed with the medicinal substance. For example, the acidic aqueous solution and the alcohol solution can be intensely stirred with a vortex mixer or the like. Although the mixing time period varies depending on the mixing mode, the mixing time period is, for example, 10 seconds to 2 minutes, and preferably 15 seconds to 1 minute.
Step 1 can be performed, for example, at ordinary temperature, or can also be performed with heating. The temperature in step 1 is, for example, 5° C. to 50° C., and preferably 15° C. to 45° C. When t-butanol is not used or when a small amount of t-butanol is used, lipid particles can be prepared even if the temperature in step 1 is relatively low. The temperature is, for example, less than 30° C., or 25° C. or less.
Step 1 can also be performed using a reaction system with a microchannel in this case, the conditions for step 1 can be suitably adjusted according to the reaction system.
After step 1, it is preferable to remove alcohol by dialysis. Water can be generally used as the dialysis solvent. The dialysis time is, for example, 4 to 48 hours, preferably 6 to 24 hours, and more preferably 6 to 12 hours. It is preferable to exchange the dialysis solvent as appropriate during dialysis.
The lipid particle of the present invention may be a frozen product, a freeze-dried product, or the like.
The present invention, according to one embodiment thereof, relates to a medical drug containing the lipid particle of the present invention (in this specification, “the medical drug of the present invention”). The lipid particle of the present invention is also usable as a reagent.
The lipid particle of the present invention enables a medicinal substance (e.g., a polynucleotide, such as siRNA) to exert its effect more efficiently, while reducing cytotoxicity. Thus, the lipid particle of the present invention can suitably be used as a carrier for a medicinal substance.
The content of the active ingredient (i.e., a medicinal substance) in the medical drug of the present invention can be suitably determined, taking into consideration, for example, the type of target disease, target therapeutic effect, administration method, treatment period, patient's age, and patient's body weight. For example, the content of the active ingredient in the medical drug of the present invention may be about 0.0001 parts by weight to 100 parts by weight, based on the entire medical drug of the present invention taken as 100 parts by weight.
The mode of administration of the medical drug of the present invention is not particularly limited, as long as a desired effect is brought about. The medical drug can be administered to mammals including humans through an administration route of either peroral administration or parenteral administration (e.g., intravenous injection, intramuscular injection, subcutaneous administration, rectal administration, transdermal administration, and local administration). The mode of administration is preferably parenteral administration, and more preferably intravenous injection. The dosage forms for peroral administration and parenteral administration and the production methods therefor are well known to those skilled in the art. Such dosage forms can be produced by mixing an active ingredient with a pharmaceutically acceptable carrier and other components, in accordance with a standard method.
The dosage form for parenteral administration includes injectable preparations e.g., drip injectable drugs, intravenous injectable drugs, intramuscularly injectable drops, subcutaneously injectable drugs, and intradermally injectable drugs), drugs for external use (e.g., ointments, cataplasms, and lotions), suppository inhalants, eye drops, ophthalmic ointments, nasal drops, and ear drops. For example, an injectable preparation can be prepared by dissolving the lipid particle of the present invention in injectable distilled water, and a solubilizing agent, a buffer, a pH adjuster, a tonicity agent, a soothing agent, a preservative, a stabilizer etc., can be optionally added thereto. The medical drug may be a freeze-dried formulation that is prepared into a drug when needed.
The medical drug of the present invention may further contain other medicinal agents effective in the treatment or prevention of diseases. The medical drug of the present invention may also optionally contain components, such as antiseptic drugs, antiphlogistics, cell activators, vitamins, and amino acids.
For the carrier for use in preparing the medical drug of the present invention, those typically used in this technical field, such as excipients, binders, disintegrants, lubricants, colorants, and flavoring agents, can be used; and stabilizers, emulsifiers, absorption promoters, surfactants, pH adjusters, antiseptics, antioxidants, fillers, moisturizers, surface activators, dispersants, buffers, preservatives, solubilizing agents, soothing agents, and the like can also optionally be used.
The dosage of the medical drug of the present invention can be determined by a practical physician, taking into consideration various factors, Such as the administration route; type of disease; degree of symptoms; patient's age, gender, and body weight; severity of disease; pharmacological findings such as pharmacokinetics and toxicological characteristics; whether a drug delivery system is used; and whether the medical drug is administered as part of a combination with other medicinal substances. The dosage of the medical drug of the present invention may be, for example, about 1 μg/kg (body weight) to 10 g/kg (body weight) per day. The dose schedule of the medical drug of the present invention can also be determined while taking into consideration the same factors as those for the dosage. For example, the medical drug of the present invention can be administered in the dosage per day described above, once daily once per month.
The following describes the present invention in detail with reference to Examples. However, the present invention is not limited to these Examples.
1,2-di-(9Z-octadecenoyl)-sn-glycero-3-phosphoethylpiperazine) (DOP-MPPZ) and 1,2-di-(9Z-octadecenoyl)-sn-glycero-3-phosphomethylpiperazine (DOP-MPPZ) were synthesized in accordance with the following scheme.
3.01 g (3.82 mmol) of DOPC was dissolved in ethyl acetate, and to the resulting solution, a 0.5 M acetate buffer with a pH of 5.5 in which 6.90 g of 1-(2-hydroxyethyl)piperazine (53 mmol) was dissolved was added, and this mixture was heated to 40° C. After heating, PLDP (phospholipase D, Asahi Kasei Pharma Corporation) (1,440 U) was added thereto, followed by stirring at 40° C. After 19 hours, elimination of DOPC was confirmed by TLC. One unit is defined as an enzyme amount with which 1 micro-mol (μmol) of a substrate is changed per minute (1 micro mol per minute) under optimum conditions (an acidity at which the chemical reaction proceeds most at a temperature of 30° C.)
The reaction mixture was diluted with chloroform, methanol, and 1-butanol (chloroform:methanol:1-butanol =30:4:1), and washed with a 20 % sodium chloride solution. After extraction and washing, the organic phase was concentrated under reduced pressure, and concentrated to dryness, thereby obtaining 3.27 g of a concentrate. The obtained crude reaction product was dissolved in 36 ml of dioxane, followed by filtration through a 0.2-μm membrane. Then, 18 ml of dioxane/4M HCl was added dropwise to the filtrate while ice-cooling, followed by stirring for 30 minutes. The white crystal precipitated after stirring was filtered, and the crystal was suspended and washed with acetone three times. The obtained crystal was vacuum-dried overnight, thereby obtaining 2.01 g of a white crystal. The obtained white crystal was dissolved in 30 mL of THF, and after ice-cooling, 80 ml of acetone was added dropwise, followed by stirring for 30 minutes in an ice bath. The white crystal precipitated after stirring was filtered, and the crystal was suspended and washed with acetone two times The obtained crystal was vacuum-dried overnight, thereby obtaining 1.71 q of a white crystal (yield: 55%).
1.00 q (1.27 mmol) of DOPC was dissolved in ethyl acetate, and to the resulting solution, a 0.5 M acetate buffer with a pH of 5.5 in which 2.55 g of 4-methylpiperazine-1-ethanol (17.7 mmol) was dissolved was added, and this mixture was heated to 40° C. After heating, PLDP (phospholipase D, Asahi Kasei Pharma Corporation) (480 U) was added thereto, followed by stirring at 40° C. After 19 hours, elimination of DOPC was confirmed by TLC. One unit is defined as an enzyme amount with which 1 micro-mol (μmol) of a substrate is changed per minute (1 micro-mol per minute) under optimum conditions (an acidity at which the 35 chemical reaction proceeds most at a temperature of 30° C.)
The reaction mixture was diluted with chloroform, methanol, and 1-butanol (chloroform:methanol:1-butanol=30:4:1), and washed with a 20 % sodium chloride solution. After extraction and washing the organic phase was concentrated under reduced pressure, and concentrated to dryness, thereby obtaining 1.15 g of a concentrate. The obtained crude reaction product was dissolved in 12.5 ml of dioxane, followed by filtration through a 0.2-μm membrane. Then, 6.8 ml of dioxane/4M HCl was added dropwise to the filtrate while ice-cooling, followed by stirring for 30 minutes. The white crystal precipitated after stirring was filtered, and the crystal was suspended and washed with acetone three times. The obtained crystal was vacuum-dried overnight, thereby obtaining 0.51 g of a white crystal. The obtained white crystal was dissolved in 4 mL of THF, and after ice-cooling, 85 ml of acetone was added dropwise, followed by stirring for 30 minutes in an ice bath. The white crystal precipitated after stirring was filtered, and the crystal was suspended and washed with acetone two times. The obtained crystal was vacuum-dried overnight, thereby obtaining 0.10 g of a white crystal (yield: 10%).
DOP-DD (DOP-DEDA) was synthesized in accordance with the following scheme. Specifically, it was synthesized in accordance with the method described in PTL 1.
An ethanol solubility test was performed based on the General Notices of the Japanese Pharmacopoeia.
100 uL of ethanol was added to 10.0 mg of DOP-PPZ, and the mixture was shaken vigorously at 60° C. for 30 seconds every 5 minutes. If DOP-PPZ was not dissolved after 30 minutes, ethanol was added and the same process was repeated. As a result, the dissolution of DOP-MPPZ was confirmed at a total addition amount of ethanol of 1.6 mL and a lipid concentration of 7.7 mM.
100 uL of ethanol was added to 10.0 mg of DOP-MPPZ, and the mixture was shaken vigorously at 20° C. for 30 seconds every 5 minutes. Since DOP-MPPZ was not dissolved after 30 minutes, 10 uL of ethanol was added, followed by shaking. As a result, the dissolution of DOP-MPPZ was confirmed at a total addition amount of ethanol of 110 uL and a lipid concentration of 110 mM.
siRNA was added to 1 mM citrate buffer (pH 4.0), thereby preparing an acidic aqueous solution of siRNA (25° C., siRNA concentration: 71.4 nM). Separately, lipids (lipid 1: DOP-DEDA, DOP-PPZ, or DOR-MPPZ; lipid 2: dipalmitoyl phosphatidylcholine (DPPC); and lipid 3: cholesterol (Chol)) at a molar ratio of 45:10:45 (lipid 1:lipid 2:lipid 3) were added to ethanol, thereby preparing a phospholipid alcohol solution (25° C., lipid concentration: 2.5 mM). A 5-fold volume of the acidic aqueous solution of siRNA was added to the phospholipid alcohol solution (siRNA/lipid molar ratio=1/7000), and a microchannel (KeyChem-Basic, YMC Co., Ltd.) was used to obtain lipid particles. Finally, ethanol was removed by dialysis.
The lipid particles were diluted 50-fold with RNase-free water, and then the particle size and polydispersity index (PDI) were measured with a Zetasizer Nano ZS (Malvern). The lipid. particles were also diluted 50-fold with a buffer (pH=4.0, 5.0, 6.0, or 7.0), and the ζ-potential was then measured.
Further, the encapsulation efficiency of RNA was measured in the following manner. The measurement was performed using an RNA assay reagent (RiboGreen reagent, Thermo Fisher Scientific), specifically as described below. A. 2% Triton-X 100 or RNase-free water was added to a lipid particle solution. The obtained solution, RNase-free water, and a RiboGreen reagent were mixed in the wells of a 96-well black plate. The plate was shaken for 5 minutes, and the fluorescence intensity in each well was measured. The encapsulation efficiency of siRNA in the lipid particles was calculated using the following equation: the encapsulation efficiency (%)=(the fluorescence intensity of total siRNA−the fluorescence intensity of free siRNA)/(the fluorescence intensity of total siRNA), with the measured fluorescence intensity.
Table 1 and
Lipid particles were produced in the same manner as in Example 2-1.
MDA-MB-231 human breast cancer cells were seeded into a 96-well plate (7×103 cells/well), and cultured at 37° C. for 24 hours. A lipid particle solution (containing 0.6/2/6 pmol of siRNA) or a lipid composite solution (containing a composite prepared using Lipofectamine (registered trademark) 2000 (Thermo Fisher Scientific), and 0.6/2/6 pmol of siRNA) was added dropwise to the wells, and the cells were cultured at 37° C. for 96 hours. The cytotoxicity of the lipid particles and lipid composite was evaluated using the Viability/Cytotoxicity Multiplex Assay Kit (Dojlindo Laboratories). 20 μL of a lysis buffer was added dropwise to the wells of the positive control group, and the cells were incubated at 37° C. for 30 minutes. 100 μL of the supernatant of each well was transferred to a 96-well clear plate, and 100 μL of LDH assay reagent of the kit was added thereto, followed by incubation at room temperature for 30 minutes. Thereafter, 50 μL of a stop solution was added thereto, and the absorbance (450 nm) was measured. In addition, the medium was removed from the plate to which attached, and 120 μL of WST-8 assay reagent (Cell Counting Kit:medium=1:9) was added to each well. After incubation at 37° C. for 5 hours, the absorbance (450 nm) was measured.
FIGS. 4 and 5 show the results.
Lipid particles were produced in the same manner as in Test Example 2-1, except that. DOP-PPZ was used as lipid 1 and PLK1 gene-targeting siRNA or non-specific siRNA was used as siRNA (si Control).
MDA-MB-231 human breast cancer cells were seeded into a 6-well plate (2×105 cells/well), and cultured at 37° C. for 24 hours. A lipid particle solution (containing 2/18 pmol of siRNA) or RNase-free water (control) was added dropwise to the wells, and the cells were cultured at 37° C. for 12 hours. The medium was exchanged, and the cells were further cultured at 37° C. for 60 hours. Using the QIAshredder and RNeasy Mini Kit (Qiagen), total RNA was extracted from the cells. Using the First-Strand cDNA Synthesis Kit (GE Healthcare Life Sciences), cDNA was synthesized from the total RNA. The cDNA was used as a template, and PLK1 mRNA levels were quantified by real-time PCR using TB Green (registered trademark) Premix Ex Tap (trademark) II (Takara Bio Inc.).
| Number | Date | Country | Kind |
|---|---|---|---|
| 2021-037573 | Mar 2021 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2022/008670 | 3/1/2022 | WO |
