JP7543259B2 - 活性剤の脂質ナノ粒子送達のための脂質 - Google Patents
活性剤の脂質ナノ粒子送達のための脂質 Download PDFInfo
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- JP7543259B2 JP7543259B2 JP2021521190A JP2021521190A JP7543259B2 JP 7543259 B2 JP7543259 B2 JP 7543259B2 JP 2021521190 A JP2021521190 A JP 2021521190A JP 2021521190 A JP2021521190 A JP 2021521190A JP 7543259 B2 JP7543259 B2 JP 7543259B2
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- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- GVOISEJVFFIGQE-YCZSINBZSA-N n-[(1r,2s,5r)-5-[methyl(propan-2-yl)amino]-2-[(3s)-2-oxo-3-[[6-(trifluoromethyl)quinazolin-4-yl]amino]pyrrolidin-1-yl]cyclohexyl]acetamide Chemical compound CC(=O)N[C@@H]1C[C@H](N(C)C(C)C)CC[C@@H]1N1C(=O)[C@@H](NC=2C3=CC(=CC=C3N=CN=2)C(F)(F)F)CC1 GVOISEJVFFIGQE-YCZSINBZSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 description 1
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000000346 nonvolatile oil Substances 0.000 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229960002969 oleic acid Drugs 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000007968 orange flavor Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229960005010 orotic acid Drugs 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229940116315 oxalic acid Drugs 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229940098695 palmitic acid Drugs 0.000 description 1
- WLJNZVDCPSBLRP-UHFFFAOYSA-N pamoic acid Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=C(C=3O)C(=O)O)=C(O)C(C(O)=O)=CC2=C1 WLJNZVDCPSBLRP-UHFFFAOYSA-N 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 235000019371 penicillin G benzathine Nutrition 0.000 description 1
- 125000005981 pentynyl group Chemical group 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 description 1
- 229940067605 phosphatidylethanolamines Drugs 0.000 description 1
- 150000003905 phosphatidylinositols Chemical class 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 150000008300 phosphoramidites Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 102000028499 poly(A) binding Human genes 0.000 description 1
- 108091023021 poly(A) binding Proteins 0.000 description 1
- 229920000768 polyamine Chemical class 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 102000054765 polymorphisms of proteins Human genes 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000001124 posttranscriptional effect Effects 0.000 description 1
- WSHYKIAQCMIPTB-UHFFFAOYSA-M potassium;2-oxo-3-(3-oxo-1-phenylbutyl)chromen-4-olate Chemical compound [K+].[O-]C=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 WSHYKIAQCMIPTB-UHFFFAOYSA-M 0.000 description 1
- OXCMYAYHXIHQOA-UHFFFAOYSA-N potassium;[2-butyl-5-chloro-3-[[4-[2-(1,2,4-triaza-3-azanidacyclopenta-1,4-dien-5-yl)phenyl]phenyl]methyl]imidazol-4-yl]methanol Chemical compound [K+].CCCCC1=NC(Cl)=C(CO)N1CC1=CC=C(C=2C(=CC=CC=2)C2=N[N-]N=N2)C=C1 OXCMYAYHXIHQOA-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical class CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 description 1
- 229960004919 procaine Drugs 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000006410 propenylene group Chemical group 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 238000002731 protein assay Methods 0.000 description 1
- 238000001243 protein synthesis Methods 0.000 description 1
- PTJWIQPHWPFNBW-GBNDHIKLSA-N pseudouridine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1C1=CNC(=O)NC1=O PTJWIQPHWPFNBW-GBNDHIKLSA-N 0.000 description 1
- 229940107700 pyruvic acid Drugs 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 210000000664 rectum Anatomy 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000010839 reverse transcription Methods 0.000 description 1
- 239000002342 ribonucleoside Substances 0.000 description 1
- 125000002652 ribonucleotide group Chemical group 0.000 description 1
- 108091092562 ribozyme Proteins 0.000 description 1
- 238000011808 rodent model Methods 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 229940116353 sebacic acid Drugs 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000001542 size-exclusion chromatography Methods 0.000 description 1
- AWUCVROLDVIAJX-GSVOUGTGSA-N sn-glycerol 3-phosphate Chemical compound OC[C@@H](O)COP(O)(O)=O AWUCVROLDVIAJX-GSVOUGTGSA-N 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 238000003797 solvolysis reaction Methods 0.000 description 1
- 210000000952 spleen Anatomy 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229960004274 stearic acid Drugs 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 229960001367 tartaric acid Drugs 0.000 description 1
- 238000001447 template-directed synthesis Methods 0.000 description 1
- ILMRJRBKQSSXGY-UHFFFAOYSA-N tert-butyl(dimethyl)silicon Chemical group C[Si](C)C(C)(C)C ILMRJRBKQSSXGY-UHFFFAOYSA-N 0.000 description 1
- 150000004685 tetrahydrates Chemical class 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 229960004559 theobromine Drugs 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 229940113082 thymine Drugs 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 230000005026 transcription initiation Effects 0.000 description 1
- 230000010474 transient expression Effects 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- 150000004684 trihydrates Chemical class 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical class CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical class OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 229960000281 trometamol Drugs 0.000 description 1
- 231100000402 unacceptable toxicity Toxicity 0.000 description 1
- 229960002703 undecylenic acid Drugs 0.000 description 1
- 241001515965 unidentified phage Species 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- 239000008215 water for injection Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
- C07C237/06—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
- A61K48/0008—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the 'non-active' part of the composition delivered, e.g. wherein such 'non-active' part is not delivered simultaneously with the 'active' part of the composition
- A61K48/0025—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the 'non-active' part of the composition delivered, e.g. wherein such 'non-active' part is not delivered simultaneously with the 'active' part of the composition wherein the non-active part clearly interacts with the delivered nucleic acid
- A61K48/0041—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the 'non-active' part of the composition delivered, e.g. wherein such 'non-active' part is not delivered simultaneously with the 'active' part of the composition wherein the non-active part clearly interacts with the delivered nucleic acid the non-active part being polymeric
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
- A61K9/1271—Non-conventional liposomes, e.g. PEGylated liposomes, liposomes coated with polymers
- A61K9/1272—Non-conventional liposomes, e.g. PEGylated liposomes, liposomes coated with polymers with substantial amounts of non-phosphatidyl, i.e. non-acylglycerophosphate, surfactants as bilayer-forming substances, e.g. cationic lipids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/51—Nanocapsules; Nanoparticles
- A61K9/5107—Excipients; Inactive ingredients
- A61K9/5123—Organic compounds, e.g. fats, sugars
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/51—Nanocapsules; Nanoparticles
- A61K9/5107—Excipients; Inactive ingredients
- A61K9/513—Organic macromolecular compounds; Dendrimers
- A61K9/5146—Organic macromolecular compounds; Dendrimers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyamines, polyanhydrides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/02—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C211/09—Diamines
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nanotechnology (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Dispersion Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
で示される化合物、または、その薬学的に許容される塩、互変異性体、または立体異性体、が提供される。
(i)疾患または病気が哺乳動物に発生するのを防ぐこと(特に、その哺乳動物がその病気になりやすいが、まだそれを有していると診断されていない場合);
(ii)疾患または病気を抑制すること(すなわち、その発症を止めること);
(iii)疾患または病気を緩和すること(すなわち、疾患または病気の退行を引き起こすこと);または、
(iv)疾患または病気に起因する症状を緩和すること(すなわち、根本の疾患または病気を対処せずに痛みを緩和すること)。
本明細書において、「疾患」および「病気」との用語は、交換可能に使用され得るか、または、特定の病気または病態が既知の原因物質を有さない(したがって、病因はまだ解明されていない)かもしれないという点で異なる可能性があり、したがって、それは、まだ疾患として認識されないが、臨床医によって多少の特定の症状が確認された望ましくない病気または症候群としてのみ認識されるものである。
一態様において、本開示は、中性脂質、荷電脂質、ステロイド、および/またはポリマー結合脂質などの他の脂質成分と組み合わせて、オリゴヌクレオチドを有する脂質ナノ粒子を形成することができる、新規な脂質化合物を提供する。理論によって拘束されるものではないが、これらの脂質ナノ粒子は、オリゴヌクレオチドを血清中での分解から保護し、インビトロおよびインビボにおいてオリゴヌクレオチドの効果的な細胞への送達を提供するものと考えられる。
G1は、-N(R3)R4、または-OR5であり;
R1は、任意に置換されていてもよい分岐の飽和または不飽和のC12-C36アルキルであり;
R2は、Lが、-C(=O)-である場合、任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC12-C36アルキルであり;あるいは、R2は、Lが、C6-C12アルキレン、C6-C12アルケニレン、またはC2-C6アルキニレンである場合、任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC4-C36アルキルであり;
R3およびR4は、それぞれ独立して、H、または任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC1-C6アルキルであり;あるいは、R3およびR4は、Lが、C6-C12アルキレン、C6-C12アルケニレン、またはC2-C6アルキニレンである場合、それぞれ独立して、任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC1-C6アルキルであり;あるいは、R3およびR4は、それらが結合している窒素と一緒になってヘテロシクリルを形成し;
R5は、H、または任意に置換されていてもよいC1-C6アルキルであり;
Lは、-C(=O)-、C6-C12アルキレン、C6-C12アルケニレン、またはC2-C12アルキニレン(例えば、C2-C6アルキニレン)であり;および、
nは、1~12の整数である。]
で示される化合物、またはその薬学的に許容される塩、互変異性体、または立体異性体、である。
G1は、-N(R3)R4、または-OR5であり;
R1は、任意に置換されていてもよい分岐の飽和または不飽和のC12-C36アルキルであり;
R2は、任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC12-C36アルキルであり;
R3およびR4は、それぞれ独立して、H、または置換されていてもよい分岐または非分岐の飽和または不飽和のC1-C6アルキルであり;あるいは、R3およびR4は、それらが結合している窒素と一緒になってヘテロシクリルを形成し;
R5は、H、または任意に置換されていてもよいC1-C6アルキルであり;
Lは、-C(=O)-であり;および、
nは、1~12の整数である、
構造(I)の化合物、またはその薬学的に許容される塩、互変異性体、または立体異性体、である。
G1は、-N(R3)R4、または-OR5であり;
R1は、任意に置換されていてもよい分岐の飽和または不飽和のC12-C36アルキルであり;
R2は、任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC4-C36アルキルであり;
R3およびR4は、それぞれ独立して、任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC1-C6アルキルであり;あるいは、R3およびR4は、それらが結合している窒素と一緒になってヘテロシクリルを形成し;
R5は、H、または任意に置換されていてもよいC1-C6アルキルであり;
Lは、C6-C12アルキレンリンカー、C6-C12アルケニレンリンカー、またはC2-C6アルキニレンリンカーであり;および、
nは、1~12の整数である、
構造(I)の化合物、またはその薬学的に許容される塩、または立体異性体、である。
R8およびR9は、それぞれ独立して、H、または任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC2-C12アルキルであり;ただし、R8およびR9は、R1が、任意に置換されていてもよい分岐の飽和または不飽和のC12-C36アルキルとなるように、それぞれ独立して選択され;および、
R10およびR11は、それぞれ独立して、H、または任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC2-C12アルキルであり;ただし、Lが-C(=O)-である場合、R2が、任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC12-C36アルキルとなり;および、LがC6-C12アルキレン、C6-C12アルケニレン、またはC2-C6アルキニレンである場合、R2が、任意に置換されていてもよい分岐または非分岐の飽和または不飽和のC4-C36アルキルとなるように、R10およびR11は、それぞれ独立して選択される。]
で示される、化合物である。
R12およびR13は、それぞれ独立して、10~30個の炭素原子を含む分岐または非分岐の飽和または不飽和のアルキル鎖であり、ここで、該アルキル鎖は、任意に、1つまたは複数のエステル結合が割り込まれていてもよく、および、
wの平均値は、30~60の範囲である。]
で示されるペグ化脂質、またはその薬学的に許容される塩、互変異性体、または立体異性体、を含む。
で示される化合物、またはその薬学的に許容される塩、互変異性体、または立体異性体、を製造するための例示的な方法を示している。当業者は、同様の方法によって、または当業者に知られている他の方法を組み合わせることによって、これらの化合物を製造することができることが理解される。また、当業者は、以下に記載されるのと同様の方法で、適切な出発成分を用い、必要に応じて合成のパラメータを変更することにより、以下に具体的に示されていない構造(I)の他の化合物を製造できることも理解される。一般に、出発成分は、Sigma Aldrich、Lancaster Synthesis,Inc.、Maybridge、Matrix Scientific、TCI、および、Fluorochem USAなどの供給元から入手するか、または当業者に知られている供給源に従って合成することができ(例えば、Advanced Organic Chemistry: Reactions, Mechanisms, and Structure, 5th edition (Wiley, December 2000)参照)、あるいは本開示に記載されたように製造することができる。
脂質ナノ粒子組成物を用いたルシフェラーゼmRNAインビボ評価
脂質ナノ粒子は、PCT公開番号WO2015/199952およびWO2017/004143に記載された一般的な方法に従って、製造および試験され、これらの開示は全て、参照により本明細書に組み込まれる。簡単に説明すると、カチオン性脂質、DSPC、コレステロール、およびPEG脂質を、約50:10:38.5:1.5、または約47.5:10:40.8:1.7のモル比で、エタノールに可溶化する。脂質ナノ粒子(LNP)を、脂質合計とmRNAとの重量比が約10:1~30:1で製造する。mRNAを、10~50mMのクエン酸または酢酸緩衝液(pH4)で、0.2mg/mLに希釈する。シリンジポンプを用いて、総流量15mL/min以上で、エタノール性脂質溶液を、mRNA水溶液と、約1:5~1:3(vol/vol)の比率で混合する。次いで、エタノールを除去し、透析によって外部のバッファーをPBSに置き換える。最後に、脂質ナノ粒子を、0.2μm細孔の滅菌フィルターでろ過する。脂質ナノ粒子の粒子サイズは、粒径約55~95nmであり、場合によっては、粒径約70~90nmであり、Malvern Zetasizer Nano ZS(Malvern、UK)を用いた準弾性光散乱によって決定される。
製剤化した脂質のPKAの測定
他の箇所で説明するように、製剤化されたカチオン性脂質のpKaは、核酸送達のLNPの有効性と相関している(Jayaraman et al, Angewandte Chemie, International Edition (2012), 51(34), 8529-8533; Semple et al, Nature Biotechnology 28, 172-176 (2010)、参照)。pKaの好ましい範囲は~5から~7である。各カチオン性脂質のpKaは、2-(p-トルイジノ)-6-ナフタレンスルホン酸(TNS)の蛍光に基づくアッセイを用いて脂質ナノ粒子で測定する。PBS中に、総脂質0.4mMの濃度で、カチオン性脂質/DSPC/コレステロール/PEG脂質(50/10/38.5/1.5mol%)を含む脂質ナノ粒子を、実施例1に記載のインラインプロセスを用いて調製する。TNSを、蒸留水中に100mMのストック溶液として調製する。ビヒクルを、10mMのHEPES、10mMのMES、10mMの酢酸アンモニウム、130mMのNaClを含む、緩衝液2mLで、脂質24mMに希釈し、ここで、pHは2.5~11の範囲とする。TNS溶液のアリコートを加えて、最終濃度1μMとし、次いで、ボルテックス混合を行い、蛍光強度を、SLM Aminco Series 2 Luminescence Spectrophotometerにより、励起および発光の波長として321nmおよび445nmを用いて、室温で測定する。シグモイドベストフィット分析を蛍光データに適用し、pKaを、最大蛍光強度の半分を生じさせるpHとして測定した。
インビボのルシフェラーゼmRNA発現げっ歯類モデルを用いた、様々なカチオン性脂質を含む脂質ナノ粒子製剤の有効性の測定
表3に示すカチオン性脂質は、以前に核酸で試験されている。比較の目的で、これらの脂質を使用して、実施例1およびPCT/US10/22614(これはその全体が参照により本明細書に組み込まれる)に記載されているインライン混合法を用いて、FLuc mRNA(L-6107)を含む脂質ナノ粒子を製剤化した。脂質ナノ粒子は、次のモル比により製剤化された:50%カチオン性脂質/10%ジステアロイルホスファチジルコリン(DSPC)/38.5%コレステロール/1.5%PEG脂質(「PEG-DMG」、すなわち、1-(モノメトキシ-ポリエチレングリコール)-2,3-ジミリストイルグリセロール、平均PEG分子量2000)。代わりの実施形態において、カチオン性脂質、DSPC、コレステロール、およびPEG脂質は、約47.5:10:40.8:1.7のモル比で製剤化した。相対活性は、実施例1に記載のように、尾静脈注射による投与4時間後の肝臓におけるルシフェラーゼ発現を測定することにより求めた。活性は、0.3mgおよび1.0mgのmRNA/kgの用量で比較し、実施例1に記載のように、投与4時間後に測定したngルシフェラーゼ/g肝臓として、表した。
化合物I-1の合成
化合物I-2の合成
化合物I-3の合成
化合物I-4の合成
化合物I-5の合成
化合物I-6の合成
化合物I-7の合成
2-ヘキシルデカノイルアミドの合成
2-ヘキシルデカン酸(26g)のベンゼン(30mL)溶液を塩化オキサリル(15mL)で処理した。気体の発生が止まるまで反応物を撹拌し、その後、溶媒を真空で除去し、残渣を真空下で4時間乾燥させた。粗製の2-ヘキシルデカノイルクロリドをジクロロメタン(100mL)に溶解し、撹拌した濃水酸化アンモニウム(150mL)の溶液にゆっくりと加えた。反応混合物を2時間放置し、水性の上澄みを取り出した。有機相を同じ方法により水で2回洗浄し、濾過した。収集した沈殿物を乾燥させて、白色の粉末として、粗製の2-ヘキシルデカノイルアミド(22g)を得た。
2-ヘキシルデカニルアミンの合成
2-ヘキシルデカノイルアミド(8.2g)の乾燥テトラヒドロフラン(40mL)懸濁液を、水素化アルミニウムリチウム(1.1g、ゆっくりと添加)で処理した。反応物を2時間撹拌し、次いで、過剰のメタノールをゆっくりと加えた。ジクロロメタン(150mL)を加え、続いて水(2mL)を加えた。反応混合物を濾過し、溶媒を濾液から除去して、粗製の2-ヘキシルデカニルアミン(4.7g)を得た。
N-(2’-ヘキシルデカニル)-2-ヘキシルデカノイルアミドの合成
2-ヘキシルデカニルアミン(4.7g)のジクロロメタン(100mL)溶液を、2-ヘキシルデカノイルクロリド(5.5g、ジクロロメタン50mLに溶解)で処理し、続いて、トリエチルアミン(4mL)で処理した。反応物を1時間撹拌し、次いで、希塩酸で洗浄した。有機相を無水硫酸マグネシウムで乾燥し、濾過し、そして、溶媒を除去した。残渣(~10g)を第2の反応からの粗生成物(~7g)と合わせ、0~10%のメタノール/ジクロロメタンのグラジエントを用いたシリカゲル(100g)に通して、N-(2’-ヘキシルデカニル)-2-ヘキシルデカノイルアミド(14.4g)を得た。
ジ-(2-ヘキシルデカニル)アミンの合成
N-(2’-ヘキシルデカニル)-2-ヘキシルデカノイルアミド(14.4g)の乾燥テトラヒドロフラン(100mL)溶液を、水素化アルミニウムリチウム(2g)で処理し、一晩還流した。過剰のメタノールをゆっくりと加え、過剰の還元剤を潰した。ジクロロメタン(200mL)を加え、続いて水(2mL)を加えた。次いで、混合物を濾過し、溶媒を除去した。残渣をヘキサンに懸濁し、濾過し、そして、溶媒を除去した。残渣を、2%酢酸/ジクロロメタン、次に2~16%のメタノール/ジクロロメタンのグラジエントを用いたシリカゲル(100g)カラムに通した。精製した画分をヘキサンと重炭酸ナトリウム水溶液で洗浄した。溶媒を除去して、無色の油として、ジ-(2-ヘキシルデカニル)アミン(9.5g)を得た。
化合物I-8の合成
化合物I-9の合成
Claims (48)
- 以下の構造(I):
G1は、-N(R3)R 4 であり;
R1は、任意に置換されていてもよい分岐の飽和のC12-C36アルキルまたは任意に置換されていてもよい分岐の不飽和のC 12 -C 36 アルキルであり;
R2は、Lが、-C(=O)-である場合、任意に置換されていてもよい分岐もしくは非分岐の飽和のC12-C36アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 12 -C 36 アルキルであり;あるいは、R2は、Lが、C6-C12アルキレン、C6-C12アルケニレン、またはC2-C6アルキニレンである場合、任意に置換されていてもよい分岐もしくは非分岐の飽和のC4-C36アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 4 -C 36 アルキルであり;
R3およびR4は、それぞれ独立して、任意に置換されていてもよい分岐もしくは非分岐の飽和のC1-C6アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 1 -C 6 アルキルであり;あるいは、R3およびR4は、それらが結合している窒素と一緒になってヘテロシクリルを形成し;
Lは、-C(=O)-、C6-C12アルキレン、C6-C12アルケニレン、またはC2-C6アルキニレンであり;および、
nは、1~12の整数である。]
で示される化合物、またはその薬学的に許容される塩、互変異性体、または立体異性体。 - G1が、-N(R3)R 4 であり;
R1が、任意に置換されていてもよい分岐の飽和のC12-C36アルキルまたは任意に置換されていてもよい分岐の不飽和のC 12 -C 36 アルキルであり;
R2が、任意に置換されていてもよい分岐もしくは非分岐の飽和のC12-C36アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 12 -C 36 アルキルであり;
R3およびR4が、それぞれ独立して、任意に置換されていてもよい分岐もしくは非分岐の飽和のC1-C6アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 1 -C 6 アルキルであり;あるいは、R3およびR4が、それらが結合している窒素と一緒になってヘテロシクリルを形成し;
Lが、-C(=O)-であり;および、
nが、1~12の整数である、
請求項1に記載の化合物、またはその薬学的に許容される塩、互変異性体、または立体異性体。 - G1が、-N(R3)R 4 であり;
R1が、任意に置換されていてもよい分岐の飽和のC12-C36アルキルまたは任意に置換されていてもよい分岐の不飽和のC 12 -C 36 アルキルであり;
R2が、任意に置換されていてもよい分岐もしくは非分岐の飽和のC4-C36アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 4 -C 36 アルキルであり;
R3およびR4が、それぞれ独立して、任意に置換されていてもよい分岐もしくは非分岐の飽和のC1-C6アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 1 -C 6 アルキルであり;あるいは、R3およびR4が、それらが結合している窒素と一緒になってヘテロシクリルを形成し;
Lが、C6-C12アルキレンリンカー、C6-C12アルケニレンリンカー、またはC2-C6アルキニレンリンカーであり;および、
nが、1~12の整数である、
請求項1に記載の化合物、またはその薬学的に許容される塩、または立体異性体。 - 以下の構造(IA):
R8およびR9は、それぞれ独立して、H、任意に置換されていてもよい分岐もしくは非分岐の飽和のC2-C12アルキル、または任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 2 -C 12 アルキルであり;ただし、R8およびR9は、R1が、任意に置換されていてもよい分岐の飽和のC12-C36アルキルまたは任意に置換されていてもよい分岐の不飽和のC 12 -C 36 アルキルとなるように、それぞれ独立して選択され;および、
R10およびR11は、それぞれ独立して、H、任意に置換されていてもよい分岐もしくは非分岐の飽和のC2-C12アルキル、または任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 2 -C 12 アルキルであり;ただし、R 10 およびR 11 は、それぞれ独立して、Lが-C(=O)-である場合、R2が、任意に置換されていてもよい分岐もしくは非分岐の飽和のC12-C36アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 12 -C 36 アルキルとなり;および、LがC6-C12アルキレン、C6-C12アルケニレン、またはC2-C6アルキニレンである場合、R2が、任意に置換されていてもよい分岐もしくは非分岐の飽和のC4-C36アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 4 -C 36 アルキルとなるように、選択される。]
で示される、請求項1~3のいずれか1項に記載の化合物。 - R8およびR9が、それぞれ独立して、任意に置換されていてもよい分岐もしくは非分岐の飽和のC2-C12アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 2 -C 12 アルキルである、請求項4に記載の化合物。
- R8が、任意に置換されていてもよい:C2アルキル、C4アルキル、C6アルキル、C8アルキル、またはC10アルキルである、請求項4または5のいずれか1項に記載の化合物。
- R8が、任意に置換されていてもよい:C4アルキル、C6アルキル、またはC8アルキルである、請求項4~6のいずれか1項に記載の化合物。
- R9が、任意に置換されていてもよい:C4アルキル、C6アルキル、C8アルキル、C10アルキル、またはC12アルキルである、請求項4~7のいずれか1項に記載の化合物。
- R9が、任意に置換されていてもよい:C6アルキル、C8アルキル、またはC10アルキルである、請求項4~8のいずれか1項に記載の化合物。
- R10およびR11が、それぞれ独立して、任意に置換されていてもよい分岐もしくは非分岐の飽和のC2-C12アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 2 -C 12 アルキルである、請求項4~9のいずれか1項に記載の化合物。
- R10が、任意に置換されていてもよい:C2アルキル、C4アルキル、C6アルキル、C8アルキル、またはC10アルキルである、請求項4~10のいずれか1項に記載の化合物。
- R10が、任意に置換されていてもよい:C4アルキル、C6アルキル、またはC8アルキルである、請求項4~11のいずれか1項に記載の化合物。
- R11が、任意に置換されていてもよい非分岐の、C2アルキル、C6アルキル、またはC10アルキルである、請求項3~12のいずれか1項に記載の化合物。
- R11が、任意に置換されていてもよいC2アルキルである、請求項13に記載の化合物。
- R11が、任意に置換されていてもよいC6アルキルである、請求項13に記載の化合物。
- R11が、任意に置換されていてもよいC10アルキルである、請求項13に記載の化合物。
- R11が、任意に置換されていてもよい:C4アルキル、C6アルキル、C8アルキル、C10アルキル、またはC12アルキルである、請求項4~12のいずれか1項に記載の化合物。
- R11が、任意に置換されていてもよい:C6アルキル、C8アルキル、またはC10アルキルである、請求項4~12のいずれか1項に記載の化合物。
- R8、R9、R10、およびR11が、それぞれ独立して、任意に置換されていてもよい分岐もしくは非分岐の飽和のC6-C10アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 6 -C 10 アルキルである、請求項4に記載の化合物。
- R8、R9、R10、およびR11が、それぞれ独立して、任意に置換されていてもよい分岐もしくは非分岐の飽和のC8-C12アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 8 -C 12 アルキルである、請求項4に記載の化合物。
- R8、R9、R10、およびR11が、それぞれ独立して、分岐もしくは非分岐の飽和のC2-C6アルキルまたは分岐もしくは非分岐の不飽和のC 2 -C 6 アルキルである、請求項4に記載の化合物。
- R8、R9、R10、およびR11が、それぞれ独立して、任意に置換されていてもよい分岐もしくは非分岐の飽和のC6-C12アルキルまたは任意に置換されていてもよい分岐もしくは非分岐の不飽和のC 6 -C 12 アルキルである、請求項4に記載の化合物。
- R1およびR2が、それぞれ独立して、任意に置換されていてもよい分岐の飽和のC12-C30アルキルまたは任意に置換されていてもよい分岐の不飽和のC 12 -C 30 アルキルである、請求項1に記載の化合物。
- R1およびR2が、それぞれ独立して、任意に置換されていてもよい分岐の飽和のC12-C20アルキルまたは任意に置換されていてもよい分岐の不飽和のC 12 -C 20 アルキルである、請求項1に記載の化合物。
- R1およびR2が、それぞれ独立して、任意に置換されていてもよい分岐の飽和のC15-C20アルキルまたは任意に置換されていてもよい分岐の不飽和のC 15 -C 20 アルキルである、請求項1に記載の化合物。
- R1およびR2が、それぞれ飽和である、請求項1または23~25のいずれか1項に記載の化合物。
- R1およびR2のうちの少なくとも1つが不飽和である、請求項1または23~25のいずれか1項に記載の化合物。
- R1およびR2が、両方とも非置換である、請求項1~27のいずれか1項に記載の化合物。
- Lが、C6-C12アルキレンである、請求項1または3~33のいずれか1項に記載の化合物。
- G1が、-N(R3)R4である、請求項1~34のいずれか1項に記載の化合物。
- G1が、-NH2、-NHCH3、または-N(CH3)2である、請求項35に記載の化合物。
- R3およびR4が、それらが結合している窒素と一緒になってヘテロシクリルを形成している、請求項35に記載の化合物。
- nが、1、2、3、4、5、または6である、請求項1~39のいずれか1項に記載の化合物。
- nが、7、8、9、10、11、または12である、請求項1~39のいずれか1項に記載の化合物。
- 請求項1~43のいずれか1項に記載の化合物、および治療剤を含む、組成物。
- 請求項1~43のいずれか1項に記載の化合物、および治療剤を含む、脂質ナノ粒子。
- 治療剤が、核酸を含む、請求項44または45のいずれか1項に記載の組成物または脂質ナノ粒子。
- 核酸が、アンチセンスRNAおよびメッセンジャーRNA(mRNA)から選択される、請求項46に記載の組成物または脂質ナノ粒子。
- 治療剤の送達のための医薬の製造における、請求項44に記載の組成物または請求項45に記載の脂質ナノ粒子の使用。
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US201862747521P | 2018-10-18 | 2018-10-18 | |
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US62/747,521 | 2018-10-18 | ||
PCT/US2019/056944 WO2020081938A1 (en) | 2018-10-18 | 2019-10-18 | Lipids for lipid nanoparticle delivery of active agents |
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