RU2013127608A - MEDICINAL PRODUCT FOR TREATMENT OF KERATOCONUS AND OTHER DEGENERATIVE DISEASES OF THE CORNEA AND PHARMACEUTICALS ON ITS BASIS - Google Patents
MEDICINAL PRODUCT FOR TREATMENT OF KERATOCONUS AND OTHER DEGENERATIVE DISEASES OF THE CORNEA AND PHARMACEUTICALS ON ITS BASIS Download PDFInfo
- Publication number
- RU2013127608A RU2013127608A RU2013127608/15A RU2013127608A RU2013127608A RU 2013127608 A RU2013127608 A RU 2013127608A RU 2013127608/15 A RU2013127608/15 A RU 2013127608/15A RU 2013127608 A RU2013127608 A RU 2013127608A RU 2013127608 A RU2013127608 A RU 2013127608A
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- Russia
- Prior art keywords
- lysine
- acid
- mixture
- drug according
- amino
- Prior art date
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- 239000003814 drug Substances 0.000 title claims abstract 42
- 201000002287 Keratoconus Diseases 0.000 title claims abstract 7
- 230000003412 degenerative effect Effects 0.000 title 1
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 229940126601 medicinal product Drugs 0.000 title 1
- 229940079593 drug Drugs 0.000 claims abstract 32
- 239000000203 mixture Substances 0.000 claims abstract 29
- 150000001413 amino acids Chemical class 0.000 claims abstract 18
- -1 amino saccharides Chemical class 0.000 claims abstract 14
- 239000002253 acid Substances 0.000 claims abstract 8
- 150000001412 amines Chemical class 0.000 claims abstract 7
- 210000004087 cornea Anatomy 0.000 claims abstract 7
- 208000015122 neurodegenerative disease Diseases 0.000 claims abstract 6
- 108010038807 Oligopeptides Chemical class 0.000 claims abstract 5
- 102000015636 Oligopeptides Human genes 0.000 claims abstract 5
- 125000000524 functional group Chemical group 0.000 claims abstract 5
- OGNSCSPNOLGXSM-UHFFFAOYSA-N 2,4-diaminobutyric acid Chemical compound NCCC(N)C(O)=O OGNSCSPNOLGXSM-UHFFFAOYSA-N 0.000 claims abstract 4
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 claims abstract 4
- 150000001414 amino alcohols Chemical class 0.000 claims abstract 4
- 229920001184 polypeptide Chemical class 0.000 claims abstract 4
- 108090000765 processed proteins & peptides Chemical class 0.000 claims abstract 4
- 102000004196 processed proteins & peptides Human genes 0.000 claims abstract 4
- AQSRRZGQRFFFGS-UHFFFAOYSA-N 2-methylpyridin-3-ol Chemical class CC1=NC=CC=C1O AQSRRZGQRFFFGS-UHFFFAOYSA-N 0.000 claims abstract 3
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims abstract 3
- 239000004472 Lysine Substances 0.000 claims abstract 3
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 claims abstract 3
- 150000001875 compounds Chemical class 0.000 claims abstract 3
- 229960003104 ornithine Drugs 0.000 claims abstract 3
- 229920000768 polyamine Chemical class 0.000 claims abstract 3
- 150000003839 salts Chemical class 0.000 claims abstract 3
- 229910052723 transition metal Inorganic materials 0.000 claims abstract 3
- 150000003624 transition metals Chemical class 0.000 claims abstract 3
- BJFWAUKOEVZCFQ-UHFFFAOYSA-N 2,10-diaminodecanoic acid Chemical compound NCCCCCCCCC(N)C(O)=O BJFWAUKOEVZCFQ-UHFFFAOYSA-N 0.000 claims abstract 2
- YKELVKGOSDUOCR-UHFFFAOYSA-N 2,12-diaminododecanoic acid Chemical compound NCCCCCCCCCCC(N)C(O)=O YKELVKGOSDUOCR-UHFFFAOYSA-N 0.000 claims abstract 2
- NMDDZEVVQDPECF-UHFFFAOYSA-N 2,7-diaminoheptanoic acid Chemical compound NCCCCCC(N)C(O)=O NMDDZEVVQDPECF-UHFFFAOYSA-N 0.000 claims abstract 2
- KMPBBRFCAYFTMR-UHFFFAOYSA-N 2,8-diaminooctanoic acid Chemical compound NCCCCCCC(N)C(O)=O KMPBBRFCAYFTMR-UHFFFAOYSA-N 0.000 claims abstract 2
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000004475 Arginine Substances 0.000 claims abstract 2
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 claims abstract 2
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 claims abstract 2
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 claims abstract 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims abstract 2
- 150000002148 esters Chemical class 0.000 claims abstract 2
- 150000003951 lactams Chemical class 0.000 claims abstract 2
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims abstract 2
- 235000001014 amino acid Nutrition 0.000 claims 12
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 5
- 239000007864 aqueous solution Substances 0.000 claims 4
- 239000000825 pharmaceutical preparation Substances 0.000 claims 4
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 claims 4
- MSWZFWKMSRAUBD-GASJEMHNSA-N 2-amino-2-deoxy-D-galactopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O MSWZFWKMSRAUBD-GASJEMHNSA-N 0.000 claims 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- 229920002125 Sokalan® Polymers 0.000 claims 3
- MSWZFWKMSRAUBD-UHFFFAOYSA-N beta-D-galactosamine Natural products NC1C(O)OC(CO)C(O)C1O MSWZFWKMSRAUBD-UHFFFAOYSA-N 0.000 claims 3
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 claims 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 3
- 239000003349 gelling agent Substances 0.000 claims 3
- 239000004584 polyacrylic acid Substances 0.000 claims 3
- 239000000243 solution Substances 0.000 claims 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims 2
- MSWZFWKMSRAUBD-IVMDWMLBSA-N 2-amino-2-deoxy-D-glucopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-IVMDWMLBSA-N 0.000 claims 2
- 229920002126 Acrylic acid copolymer Polymers 0.000 claims 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
- 239000004743 Polypropylene Substances 0.000 claims 2
- 239000005700 Putrescine Substances 0.000 claims 2
- RADKZDMFGJYCBB-UHFFFAOYSA-N Pyridoxal Chemical compound CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 claims 2
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 claims 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims 2
- 125000005250 alkyl acrylate group Chemical group 0.000 claims 2
- 229920001577 copolymer Polymers 0.000 claims 2
- 210000000744 eyelid Anatomy 0.000 claims 2
- 235000018977 lysine Nutrition 0.000 claims 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N n-Decanedioic acid Natural products OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims 2
- 235000007682 pyridoxal 5'-phosphate Nutrition 0.000 claims 2
- 239000011589 pyridoxal 5'-phosphate Substances 0.000 claims 2
- 229960001327 pyridoxal phosphate Drugs 0.000 claims 2
- NHZMQXZHNVQTQA-UHFFFAOYSA-N pyridoxamine Chemical compound CC1=NC=C(CO)C(CN)=C1O NHZMQXZHNVQTQA-UHFFFAOYSA-N 0.000 claims 2
- LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 claims 2
- ATHGHQPFGPMSJY-UHFFFAOYSA-N spermidine Chemical compound NCCCCNCCCN ATHGHQPFGPMSJY-UHFFFAOYSA-N 0.000 claims 2
- PFNFFQXMRSDOHW-UHFFFAOYSA-N spermine Chemical compound NCCCNCCCCNCCCN PFNFFQXMRSDOHW-UHFFFAOYSA-N 0.000 claims 2
- UODZHRGDSPLRMD-UHFFFAOYSA-N sym-homospermidine Chemical compound NCCCCNCCCCN UODZHRGDSPLRMD-UHFFFAOYSA-N 0.000 claims 2
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 claims 1
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 claims 1
- OGDDUPYYEQZVHV-KDDYFZQKSA-N (2s)-2-amino-5-(diaminomethylideneamino)pentanoic acid;(2s)-2,6-diaminohexanoic acid Chemical compound NCCCC[C@H](N)C(O)=O.OC(=O)[C@@H](N)CCCNC(N)=N OGDDUPYYEQZVHV-KDDYFZQKSA-N 0.000 claims 1
- OXUKFGQDYVWXTL-DKDCSSFGSA-N (3R,4R,5R,6R)-3-amino-6-methyloxane-2,4,5-triol (2R,3R,4S,5R)-2-amino-3,4,5-trihydroxyhexanal Chemical compound C[C@@H](O)[C@H](O)[C@H](O)[C@@H](N)C=O.C[C@H]1OC(O)[C@H](N)[C@@H](O)[C@H]1O OXUKFGQDYVWXTL-DKDCSSFGSA-N 0.000 claims 1
- IMGXDCAOBSTOQJ-OYDNGPRDSA-N (3S,4R,5S,6R)-3-amino-6-(hydroxymethyl)oxane-2,4,5-triol (2S,3R,4S,5R)-2-amino-3,4,5,6-tetrahydroxyhexanal Chemical compound O=C[C@@H](N)[C@@H](O)[C@H](O)[C@H](O)CO.N[C@@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O IMGXDCAOBSTOQJ-OYDNGPRDSA-N 0.000 claims 1
- FFJCNSLCJOQHKM-CLFAGFIQSA-N (z)-1-[(z)-octadec-9-enoxy]octadec-9-ene Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCCCCCCC\C=C/CCCCCCCC FFJCNSLCJOQHKM-CLFAGFIQSA-N 0.000 claims 1
- NKJOXAZJBOMXID-UHFFFAOYSA-N 1,1'-Oxybisoctane Chemical compound CCCCCCCCOCCCCCCCC NKJOXAZJBOMXID-UHFFFAOYSA-N 0.000 claims 1
- 229940058015 1,3-butylene glycol Drugs 0.000 claims 1
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 claims 1
- CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 claims 1
- PZSFTBARUSGJTA-UHFFFAOYSA-N 1-n-(4-aminobutyl)butane-1,3-diamine Chemical compound CC(N)CCNCCCCN PZSFTBARUSGJTA-UHFFFAOYSA-N 0.000 claims 1
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 claims 1
- HANWHVWXFQSQGJ-UHFFFAOYSA-N 1-tetradecoxytetradecane Chemical compound CCCCCCCCCCCCCCOCCCCCCCCCCCCCC HANWHVWXFQSQGJ-UHFFFAOYSA-N 0.000 claims 1
- TXYKVMGAIGVXFY-UHFFFAOYSA-N 1-undecoxyundecane Chemical compound CCCCCCCCCCCOCCCCCCCCCCC TXYKVMGAIGVXFY-UHFFFAOYSA-N 0.000 claims 1
- KEBGMMXWUKWKGB-UHFFFAOYSA-N 2,9-diaminononanoic acid Chemical compound NCCCCCCCC(N)C(O)=O KEBGMMXWUKWKGB-UHFFFAOYSA-N 0.000 claims 1
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- NIQFAJBKEHPUAM-UHFFFAOYSA-N 2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]ethanamine Chemical compound NCCOCCOCCOCCN NIQFAJBKEHPUAM-UHFFFAOYSA-N 0.000 claims 1
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- ZAXCZCOUDLENMH-UHFFFAOYSA-N 3,3,3-tetramine Chemical compound NCCCNCCCNCCCN ZAXCZCOUDLENMH-UHFFFAOYSA-N 0.000 claims 1
- JCEZOHLWDIONSP-UHFFFAOYSA-N 3-[2-[2-(3-aminopropoxy)ethoxy]ethoxy]propan-1-amine Chemical compound NCCCOCCOCCOCCCN JCEZOHLWDIONSP-UHFFFAOYSA-N 0.000 claims 1
- YOOSAIJKYCBPFW-UHFFFAOYSA-N 3-[4-(3-aminopropoxy)butoxy]propan-1-amine Chemical compound NCCCOCCCCOCCCN YOOSAIJKYCBPFW-UHFFFAOYSA-N 0.000 claims 1
- 125000004042 4-aminobutyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])N([H])[H] 0.000 claims 1
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- CERZMXAJYMMUDR-UHFFFAOYSA-N neuraminic acid Natural products NC1C(O)CC(O)(C(O)=O)OC1C(O)C(O)CO CERZMXAJYMMUDR-UHFFFAOYSA-N 0.000 claims 1
- 230000003472 neutralizing effect Effects 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 229920000729 poly(L-lysine) polymer Polymers 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 108010055896 polyornithine Proteins 0.000 claims 1
- 229920001155 polypropylene Polymers 0.000 claims 1
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims 1
- NGVDGCNFYWLIFO-UHFFFAOYSA-N pyridoxal 5'-phosphate Chemical compound CC1=NC=C(COP(O)(O)=O)C(C=O)=C1O NGVDGCNFYWLIFO-UHFFFAOYSA-N 0.000 claims 1
- 235000008151 pyridoxamine Nutrition 0.000 claims 1
- 239000011699 pyridoxamine Substances 0.000 claims 1
- 235000008160 pyridoxine Nutrition 0.000 claims 1
- 239000011677 pyridoxine Substances 0.000 claims 1
- WHOMFKWHIQZTHY-UHFFFAOYSA-L pyridoxine 5'-phosphate(2-) Chemical compound CC1=NC=C(COP([O-])([O-])=O)C(CO)=C1O WHOMFKWHIQZTHY-UHFFFAOYSA-L 0.000 claims 1
- 235000019170 pyridoxine-5-phosphate Nutrition 0.000 claims 1
- 239000011763 pyridoxine-5-phosphate Substances 0.000 claims 1
- 229940107700 pyruvic acid Drugs 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 159000000000 sodium salts Chemical class 0.000 claims 1
- 229940075582 sorbic acid Drugs 0.000 claims 1
- 239000000600 sorbitol Substances 0.000 claims 1
- 229940063673 spermidine Drugs 0.000 claims 1
- 229940063675 spermine Drugs 0.000 claims 1
- WPLOVIFNBMNBPD-ATHMIXSHSA-N subtilin Chemical compound CC1SCC(NC2=O)C(=O)NC(CC(N)=O)C(=O)NC(C(=O)NC(CCCCN)C(=O)NC(C(C)CC)C(=O)NC(=C)C(=O)NC(CCCCN)C(O)=O)CSC(C)C2NC(=O)C(CC(C)C)NC(=O)C1NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C1NC(=O)C(=C/C)/NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C2NC(=O)CNC(=O)C3CCCN3C(=O)C(NC(=O)C3NC(=O)C(CC(C)C)NC(=O)C(=C)NC(=O)C(CCC(O)=O)NC(=O)C(NC(=O)C(CCCCN)NC(=O)C(N)CC=4C5=CC=CC=C5NC=4)CSC3)C(C)SC2)C(C)C)C(C)SC1)CC1=CC=CC=C1 WPLOVIFNBMNBPD-ATHMIXSHSA-N 0.000 claims 1
- 239000011975 tartaric acid Substances 0.000 claims 1
- 235000002906 tartaric acid Nutrition 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 229940011671 vitamin b6 Drugs 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Classifications
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A61K31/785—Polymers containing nitrogen
- A61K31/787—Polymers containing nitrogen containing heterocyclic rings having nitrogen as a ring hetero atom
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/133—Amines having hydroxy groups, e.g. sphingosine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
- A61K31/198—Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/223—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of alpha-aminoacids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7088—Compounds having three or more nucleosides or nucleotides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A61K31/765—Polymers containing oxygen
- A61K31/78—Polymers containing oxygen of acrylic acid or derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/02—Peptides of undefined number of amino acids; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/05—Dipeptides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/06—Tripeptides
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- 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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0048—Eye, e.g. artificial tears
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- 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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0048—Eye, e.g. artificial tears
- A61K9/0051—Ocular inserts, ocular implants
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
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- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Ophthalmology & Optometry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Gastroenterology & Hepatology (AREA)
- Molecular Biology (AREA)
- Emergency Medicine (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
1. Лекарственное средство для лечения кератоконуса и других дегенеративных заболеваний роговицы, содержащее в качестве активного компонента эффективное количество амина с функциональными группами в виде соли или в составе комплексного соединения переходного металла или их смеси.2. Лекарственное средство по п.1, отличающееся тем, что в качестве амина с функциональными группами используют аминоспирты, или аминокислоты, или производные аминокислот, или олигопептиды, или полипептиды, или полиамины, или производные 3-гидрокси-2-метилпиридина, или аминосахариды или их смесь.3. Лекарственное средство по п.2, отличающееся тем, что в качестве аминоспиртов используют 2-амино-2-метил-1,3-пропандиол или трис(гидроксиметил)аминометан или их смесь.4. Лекарственное средство по п.2, отличающееся тем, что в качестве аминокислот используют 2,4-диаминобутановую кислоту или орнитин, или лизин, или гидроксилизин, или 2,7-диаминогептановую кислоту, или 2,8-диаминооктановую кислоту, или 2,9-диаминононановую кислота, или 2,10-диаминодекановую кислоту, или 2,12-диаминододекановую кислоту, или аргинин или их смесь.5. Лекарственное средство по п.4, отличающееся тем, что в качестве аминокислот используют D- или L-оптические изомеры аминокислот или их D, L-смесь (рацемат).6. Лекарственное средство по п.2, отличающееся тем, что в качестве производных аминокислот используют лактам одной из аминокислот по пп.4 и 5 или смесь лактамов аминокислот по пп.4 и 5.7. Лекарственное средство по п.2, отличающееся тем, что в качестве производных аминокислот используют сложный эфир одной их аминокислот по пп.4 и 5 или смесь сложных эфиров аминокислот по пп.4 и 5.8. Лекарственное сре�1. A medicine for the treatment of keratoconus and other degenerative diseases of the cornea, containing as an active component an effective amount of an amine with functional groups in the form of a salt or as part of a transition metal complex compound or a mixture thereof. The medicine according to claim 1, characterized in that amino alcohols, or amino acids, or derivatives of amino acids, or oligopeptides, or polypeptides, or polyamines, or derivatives of 3-hydroxy-2-methylpyridine, or amino saccharides, are used as an amine with functional groups mixture. 3. The medicine according to claim 2, characterized in that 2-amino-2-methyl-1,3-propanediol or Tris (hydroxymethyl) aminomethane or a mixture thereof are used as amino alcohols. The medicine according to claim 2, characterized in that 2,4-diaminobutanoic acid or ornithine, or lysine, or hydroxylisine, or 2,7-diaminoheptanoic acid, or 2,8-diamino-octanoic acid, or 2.9 are used as amino acids. -diaminononanoic acid, or 2,10-diaminodecanoic acid, or 2,12-diaminododecanoic acid, or arginine, or a mixture thereof. 5. The medicine according to claim 4, characterized in that the D- or L-optical isomers of the amino acids or their D, L-mixture (racemate) are used as amino acids. The drug according to claim 2, characterized in that the derivatives of amino acids use the lactam of one of the amino acids according to claims 4 and 5, or a mixture of the amino acid lactams according to claims 4 and 5.7. The drug according to claim 2, characterized in that the ester of one of the amino acids according to claims 4 and 5 or a mixture of amino acid esters according to claims 4 and 5.8 are used as derivatives of amino acids. Medication
Claims (32)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
RU2013127608A RU2683651C2 (en) | 2013-06-18 | 2013-06-18 | Medicine for treatment of keraticonus and other degenerative diseases of cornea and pharmaceutical agents based thereon |
PCT/RU2014/000438 WO2014204357A2 (en) | 2013-06-18 | 2014-06-17 | Drug for the treatment of keratoconus and other degenerative disorders of the cornea and pharmaceutical preparations on the basis thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
RU2013127608A RU2683651C2 (en) | 2013-06-18 | 2013-06-18 | Medicine for treatment of keraticonus and other degenerative diseases of cornea and pharmaceutical agents based thereon |
Publications (2)
Publication Number | Publication Date |
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RU2013127608A true RU2013127608A (en) | 2014-12-27 |
RU2683651C2 RU2683651C2 (en) | 2019-04-01 |
Family
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RU2013127608A RU2683651C2 (en) | 2013-06-18 | 2013-06-18 | Medicine for treatment of keraticonus and other degenerative diseases of cornea and pharmaceutical agents based thereon |
Country Status (2)
Country | Link |
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RU (1) | RU2683651C2 (en) |
WO (1) | WO2014204357A2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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AU2016396661B2 (en) * | 2016-03-08 | 2023-01-19 | University Of Utah Research Foundation | Cross-linking agents and associated methods |
TWI826685B (en) | 2019-05-02 | 2023-12-21 | 瑞士商愛爾康公司 | Dissolvable polymeric eye inserts and method of using same |
CN114225016B (en) * | 2021-12-02 | 2024-07-09 | 北京大学第一医院 | Method for inhibiting myopia and keratoconus progression |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6395029B1 (en) * | 1999-01-19 | 2002-05-28 | The Children's Hospital Of Philadelphia | Sustained delivery of polyionic bioactive agents |
GB0112324D0 (en) * | 2001-05-21 | 2001-07-11 | Croda Int Plc | Compounds |
US20060166879A1 (en) * | 2002-12-20 | 2006-07-27 | Chakshu Research Inc | Treatment of conditions associated with the presence of macromolecular aggregates, particularly ophthalmic disorders |
ES2613027T3 (en) * | 2004-08-18 | 2017-05-22 | Novabiotics Limited | Antibacterial peptides |
TW200716140A (en) * | 2005-06-17 | 2007-05-01 | Dynamis Therapeutics Inc | Treatment of inflammatory conditions |
EP2148667B1 (en) * | 2007-04-12 | 2013-05-22 | Waratah Pharmaceuticals, Inc. | Use of cyclohexanehexol derivatives in the treatment of ocular diseases |
RU2352589C1 (en) * | 2007-12-11 | 2009-04-20 | Сергей Иванович Белых | Method for producing biosoluble copolymers of acrylamide, vinylpyrrolidone and alkylacrylate |
CA2805511C (en) * | 2009-07-27 | 2017-04-11 | Sanseverino, Renato | Ophthalmic solution for protecting internal structures of the eyeball against uv-a rays or for the treatment of keratoconus with a trans-epithelial cross-linking technique |
US10294315B2 (en) * | 2009-09-30 | 2019-05-21 | Nippon Shokubai Co., Ltd. | Polyacrylic acid (salt)-based water absorbent resin and method for producing same |
US20140322193A1 (en) * | 2011-12-02 | 2014-10-30 | Michael Kaleko | Therapies for Disorders of the Cornea and Conjunctiva |
-
2013
- 2013-06-18 RU RU2013127608A patent/RU2683651C2/en not_active IP Right Cessation
-
2014
- 2014-06-17 WO PCT/RU2014/000438 patent/WO2014204357A2/en active Application Filing
Also Published As
Publication number | Publication date |
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RU2683651C2 (en) | 2019-04-01 |
WO2014204357A3 (en) | 2015-03-12 |
WO2014204357A2 (en) | 2014-12-24 |
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