CN100337621C - 门冬氨酸及其盐的用途 - Google Patents
门冬氨酸及其盐的用途 Download PDFInfo
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- CN100337621C CN100337621C CNB2004100734389A CN200410073438A CN100337621C CN 100337621 C CN100337621 C CN 100337621C CN B2004100734389 A CNB2004100734389 A CN B2004100734389A CN 200410073438 A CN200410073438 A CN 200410073438A CN 100337621 C CN100337621 C CN 100337621C
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- Prior art keywords
- aspartic acid
- preparation
- eye drop
- aspartate
- cataract
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- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 title claims abstract description 67
- 235000003704 aspartic acid Nutrition 0.000 title claims abstract description 58
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 title claims abstract description 58
- 150000003839 salts Chemical class 0.000 title abstract description 14
- 208000002177 Cataract Diseases 0.000 claims abstract description 38
- 239000003889 eye drop Substances 0.000 claims abstract description 35
- 239000003814 drug Substances 0.000 claims abstract description 24
- 238000002360 preparation method Methods 0.000 claims abstract description 19
- 201000008525 senile cataract Diseases 0.000 claims abstract description 16
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 9
- 239000007924 injection Substances 0.000 claims abstract description 8
- 238000002347 injection Methods 0.000 claims abstract description 8
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 7
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 7
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 7
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 6
- 239000000126 substance Substances 0.000 claims abstract description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 14
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 8
- 239000011777 magnesium Substances 0.000 claims description 8
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 6
- 229940009098 aspartate Drugs 0.000 claims description 6
- 239000011591 potassium Substances 0.000 claims description 6
- 239000011734 sodium Substances 0.000 claims description 6
- 239000011701 zinc Substances 0.000 claims description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 5
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 238000012377 drug delivery Methods 0.000 claims description 3
- 238000009472 formulation Methods 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 210000000214 mouth Anatomy 0.000 claims description 3
- 239000002552 dosage form Substances 0.000 claims 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims 1
- 239000013078 crystal Substances 0.000 abstract description 21
- 208000034699 Vitreous floaters Diseases 0.000 abstract description 16
- 229940079593 drug Drugs 0.000 abstract description 6
- 229940012356 eye drops Drugs 0.000 abstract description 3
- 230000003405 preventing effect Effects 0.000 abstract description 3
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 abstract 2
- 230000003064 anti-oxidating effect Effects 0.000 abstract 1
- 229960001230 asparagine Drugs 0.000 abstract 1
- 229960005261 aspartic acid Drugs 0.000 description 49
- 238000011282 treatment Methods 0.000 description 25
- 230000000694 effects Effects 0.000 description 19
- WTWSHHITWMVLBX-DKWTVANSSA-M sodium;(2s)-2-aminobutanedioate;hydron Chemical compound [Na+].[O-]C(=O)[C@@H](N)CC(O)=O WTWSHHITWMVLBX-DKWTVANSSA-M 0.000 description 15
- WQZGKKKJIJFFOK-SVZMEOIVSA-N (+)-Galactose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-SVZMEOIVSA-N 0.000 description 10
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- 239000000902 placebo Substances 0.000 description 5
- 229940068196 placebo Drugs 0.000 description 5
- WSMYVTOQOOLQHP-UHFFFAOYSA-N Malondialdehyde Chemical compound O=CCC=O WSMYVTOQOOLQHP-UHFFFAOYSA-N 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 210000000695 crystalline len Anatomy 0.000 description 4
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- ISYHFARMUCCYDZ-DKWTVANSSA-N (2s)-2-aminobutanedioic acid;magnesium Chemical compound [Mg].OC(=O)[C@@H](N)CC(O)=O ISYHFARMUCCYDZ-DKWTVANSSA-N 0.000 description 3
- 206010019280 Heart failures Diseases 0.000 description 3
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 description 3
- 206010024214 Lenticular opacities Diseases 0.000 description 3
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 3
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 230000002362 anti-crystal effect Effects 0.000 description 2
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- 210000003470 mitochondria Anatomy 0.000 description 2
- 208000010125 myocardial infarction Diseases 0.000 description 2
- 239000002773 nucleotide Substances 0.000 description 2
- 125000003729 nucleotide group Chemical group 0.000 description 2
- KHPXUQMNIQBQEV-UHFFFAOYSA-N oxaloacetic acid Chemical compound OC(=O)CC(=O)C(O)=O KHPXUQMNIQBQEV-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000001575 pathological effect Effects 0.000 description 2
- 229910001414 potassium ion Inorganic materials 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 210000002460 smooth muscle Anatomy 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000001384 succinic acid Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 238000002560 therapeutic procedure Methods 0.000 description 2
- 230000004102 tricarboxylic acid cycle Effects 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 206010002660 Anoxia Diseases 0.000 description 1
- 241000976983 Anoxia Species 0.000 description 1
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- 101100027969 Caenorhabditis elegans old-1 gene Proteins 0.000 description 1
- 206010008909 Chronic Hepatitis Diseases 0.000 description 1
- CKLJMWTZIZZHCS-UHFFFAOYSA-N D-OH-Asp Natural products OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 description 1
- 206010016825 Flushing Diseases 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- RKUNBYITZUJHSG-UHFFFAOYSA-N Hyosciamin-hydrochlorid Natural products CN1C(C2)CCC1CC2OC(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-UHFFFAOYSA-N 0.000 description 1
- 206010020575 Hyperammonaemia Diseases 0.000 description 1
- 206010021143 Hypoxia Diseases 0.000 description 1
- CKLJMWTZIZZHCS-UWTATZPHSA-N L-Aspartic acid Natural products OC(=O)[C@H](N)CC(O)=O CKLJMWTZIZZHCS-UWTATZPHSA-N 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 208000006550 Mydriasis Diseases 0.000 description 1
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- 229960000396 atropine Drugs 0.000 description 1
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- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
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- 239000001569 carbon dioxide Substances 0.000 description 1
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000000747 cardiac effect Effects 0.000 description 1
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- 230000003859 lipid peroxidation Effects 0.000 description 1
- 230000003908 liver function Effects 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
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- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
阶段 | 级别 | 晶体浑浊度 | 分值 |
正常12345 | ABCD | 晶体澄清晶体周边出现细小空泡赤道部有空泡细带空泡占晶体前皮质面积的1/3空泡占晶体前皮质面积的2/3空泡液化或出现乳光或出现极少量点状、条状白色浑浊晶体散在片状白色沉淀晶体核开始浑浊晶体核全部浑浊 | 00.10.40.71.02.03.04.05.0 |
组别 | 晶体数 | 用药后25天大鼠晶体浑浊度分值 |
正常对照组模型组门冬氨酸高剂量(6次/日)门冬氨酸低剂量(3次/日)门冬氨酸钠高剂量(6次/日)门冬氨酸钠低剂量(3次/日) | 202020202020 | 03.24±1.601.73±1.122)2.24±1.171)1.51±1.252)2.18±1.191) |
组别 | 动物数 | 药物浓度(g/100ml) | MDA(nmol/mg晶体) |
正常对照组病理模型组 | 1010 | 生理盐水生理盐水 | 0.29±0.032)0.68±0.10 |
门冬氨酸高剂量组门冬氨酸低剂量组门冬氨酸钠高剂量组门冬氨酸钠低剂量组 | 10101010 | 6次/日3次/日6次/日3次/日 | 0.35±0.042)0.47±0.062)0.37±0.052)0.45±0.072) |
Claims (4)
Priority Applications (1)
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CNB2004100734389A CN100337621C (zh) | 2004-12-15 | 2004-12-15 | 门冬氨酸及其盐的用途 |
Applications Claiming Priority (1)
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CNB2004100734389A CN100337621C (zh) | 2004-12-15 | 2004-12-15 | 门冬氨酸及其盐的用途 |
Publications (2)
Publication Number | Publication Date |
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CN1660063A CN1660063A (zh) | 2005-08-31 |
CN100337621C true CN100337621C (zh) | 2007-09-19 |
Family
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CNB2004100734389A Expired - Fee Related CN100337621C (zh) | 2004-12-15 | 2004-12-15 | 门冬氨酸及其盐的用途 |
Country Status (1)
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CN (1) | CN100337621C (zh) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH1017487A (ja) * | 1996-06-25 | 1998-01-20 | Asahi Glass Co Ltd | 後発白内障予防薬 |
JP2001187733A (ja) * | 1999-12-28 | 2001-07-10 | Lion Corp | コンタクトレンズ用眼科組成物 |
JP2003128553A (ja) * | 2001-08-15 | 2003-05-08 | Rohto Pharmaceut Co Ltd | 眼科用組成物 |
-
2004
- 2004-12-15 CN CNB2004100734389A patent/CN100337621C/zh not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH1017487A (ja) * | 1996-06-25 | 1998-01-20 | Asahi Glass Co Ltd | 後発白内障予防薬 |
JP2001187733A (ja) * | 1999-12-28 | 2001-07-10 | Lion Corp | コンタクトレンズ用眼科組成物 |
JP2003128553A (ja) * | 2001-08-15 | 2003-05-08 | Rohto Pharmaceut Co Ltd | 眼科用組成物 |
Non-Patent Citations (1)
Title |
---|
门冬氨酸阿奇霉素滴眼液的制备与临床应用 邓智建 张永恒 曹冬梅,中国医院药学杂志,第22卷第8期 2002 * |
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C41 | Transfer of patent application or patent right or utility model | ||
C56 | Change in the name or address of the patentee | ||
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Address after: 311300 Ling'an Economic Development Zone, Zhejiang Patentee after: YIFAN XINFU PHARMACEUTICAL Co.,Ltd. Address before: 311300 Ling'an Economic Development Zone, Zhejiang Patentee before: ZHEJIANG HANGZHOU XINFU PHARMACEUTICAL Co.,Ltd. |
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Effective date of registration: 20160720 Address after: Hangzhou City, Zhejiang province 311300 Ling'an City Kam South Street No. 9 Gua fan Patentee after: HANGZHOU XINFU SCIENCE & TECHNOLOGY Co.,Ltd. Address before: 311300 Ling'an Economic Development Zone, Zhejiang Patentee before: YIFAN XINFU PHARMACEUTICAL Co.,Ltd. |
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Granted publication date: 20070919 Termination date: 20201215 |