JPH0510328B2 - - Google Patents
Info
- Publication number
- JPH0510328B2 JPH0510328B2 JP59123581A JP12358184A JPH0510328B2 JP H0510328 B2 JPH0510328 B2 JP H0510328B2 JP 59123581 A JP59123581 A JP 59123581A JP 12358184 A JP12358184 A JP 12358184A JP H0510328 B2 JPH0510328 B2 JP H0510328B2
- Authority
- JP
- Japan
- Prior art keywords
- fad
- present
- polyvinylpyrrolidone
- borax
- paraoxybenzoate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 235000019162 flavin adenine dinucleotide Nutrition 0.000 claims description 16
- 239000011714 flavin adenine dinucleotide Substances 0.000 claims description 16
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 10
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 10
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 10
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 8
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 8
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 7
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 7
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 7
- 239000003889 eye drop Substances 0.000 claims description 6
- VWWQXMAJTJZDQX-UYBVJOGSSA-N flavin adenine dinucleotide Chemical compound C1=NC2=C(N)N=CN=C2N1[C@@H]([C@H](O)[C@@H]1O)O[C@@H]1CO[P@](O)(=O)O[P@@](O)(=O)OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C2=NC(=O)NC(=O)C2=NC2=C1C=C(C)C(C)=C2 VWWQXMAJTJZDQX-UYBVJOGSSA-N 0.000 claims description 2
- 229940093632 flavin-adenine dinucleotide Drugs 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 239000002244 precipitate Substances 0.000 description 7
- 229910021538 borax Inorganic materials 0.000 description 6
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 6
- 239000004327 boric acid Substances 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
- 239000004328 sodium tetraborate Substances 0.000 description 6
- 235000010339 sodium tetraborate Nutrition 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229940012356 eye drops Drugs 0.000 description 4
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- VTAJIXDZFCRWBR-UHFFFAOYSA-N Licoricesaponin B2 Natural products C1C(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2)C(O)=O)C)(C)CC2)(C)C2C(C)(C)CC1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O VTAJIXDZFCRWBR-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 description 3
- 229960004949 glycyrrhizic acid Drugs 0.000 description 3
- UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 description 3
- 239000001685 glycyrrhizic acid Substances 0.000 description 3
- 235000019410 glycyrrhizin Nutrition 0.000 description 3
- 239000002997 ophthalmic solution Substances 0.000 description 3
- 229940054534 ophthalmic solution Drugs 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000008213 purified water Substances 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- 238000011146 sterile filtration Methods 0.000 description 3
- 239000013068 control sample Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000013112 stability test Methods 0.000 description 2
- 229910052724 xenon Inorganic materials 0.000 description 2
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 2
- -1 Alternatively Polymers 0.000 description 1
- BIVBRWYINDPWKA-VLQRKCJKSA-L Glycyrrhizinate dipotassium Chemical compound [K+].[K+].O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@H]1CC[C@]2(C)[C@H]3C(=O)C=C4[C@@H]5C[C@](C)(CC[C@@]5(CC[C@@]4(C)[C@]3(C)CC[C@H]2C1(C)C)C)C(O)=O)C([O-])=O)[C@@H]1O[C@H](C([O-])=O)[C@@H](O)[C@H](O)[C@H]1O BIVBRWYINDPWKA-VLQRKCJKSA-L 0.000 description 1
- 239000003708 ampul Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 229940101029 dipotassium glycyrrhizinate Drugs 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 229940074774 glycyrrhizinate Drugs 0.000 description 1
- 125000005113 hydroxyalkoxy group Chemical group 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Landscapes
- Saccharide Compounds (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12358184A JPS615018A (ja) | 1984-06-15 | 1984-06-15 | 安定な点眼液 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12358184A JPS615018A (ja) | 1984-06-15 | 1984-06-15 | 安定な点眼液 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS615018A JPS615018A (ja) | 1986-01-10 |
| JPH0510328B2 true JPH0510328B2 (fr) | 1993-02-09 |
Family
ID=14864129
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12358184A Granted JPS615018A (ja) | 1984-06-15 | 1984-06-15 | 安定な点眼液 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS615018A (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6391331A (ja) * | 1986-10-03 | 1988-04-22 | Senjiyu Seiyaku Kk | 眼科用水性組成物 |
| WO1998043643A1 (fr) * | 1997-04-01 | 1998-10-08 | Toa Medicine Co., Ltd. | Preparations d'une solution aqueuse d'acyclovir |
| JP4919666B2 (ja) * | 2005-01-26 | 2012-04-18 | ロート製薬株式会社 | プラノプロフェン含有組成物 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5512886A (en) * | 1978-05-05 | 1980-01-29 | Akzo Nv | Composite yarn and method |
| JPS5518689A (en) * | 1978-07-24 | 1980-02-08 | May Randall Lee | Electroacoustic amplifying drum |
-
1984
- 1984-06-15 JP JP12358184A patent/JPS615018A/ja active Granted
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5512886A (en) * | 1978-05-05 | 1980-01-29 | Akzo Nv | Composite yarn and method |
| JPS5518689A (en) * | 1978-07-24 | 1980-02-08 | May Randall Lee | Electroacoustic amplifying drum |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS615018A (ja) | 1986-01-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE60209145T2 (de) | Pharmazeutische formulierungen mit platinderivaten | |
| WO2001032181A2 (fr) | Compositions pharmaceutiques contenant un medicament antibiotique de fluoroquinolone et une gomme xanthan | |
| SA97180473A (ar) | "'بيرولات مستبدلة" | |
| EP0271795A3 (fr) | Dérivés de l'octahydro-10-oxo-6H-pyridazo[1,2-a][112]diazépine, intermédiaires et procédé pour leur préparation ainsi que médicament les contenant | |
| NL8303657A (nl) | Voor injectie geschikte, stabiele, waterige, zoutzuur bevattende oplossing van cisplatine, alsmede werkwijze ter bereiding daarvan. | |
| SE451840B (sv) | Optiskt rent monohydrat av s-(-)-1-propyl-2',6'-pipekoloxylididhydroklorid, sett att framstella denna och farmaceutiska beredningar for lokalbedovning | |
| DE19500784A1 (de) | Enrofloxacin-Injektions- oder Infusionslösungen | |
| TWI406675B (zh) | Pharmaceutical composition | |
| DE69001111T2 (de) | Antikrebs-zusammensetzung. | |
| JPH0510328B2 (fr) | ||
| JPH0696533B2 (ja) | キノロンカルボン酸の水性組成物 | |
| PT93571B (pt) | Processo para a preparacao do acido (s)-7-(3-amino-1-pirrolidinil)-1-ciclopropil -6-fluoro-1,4-dihidro-4-oxo-1,8-naftiridino-3-carboxilico e de composicoes farmaceuticas que o contem | |
| BG61368B2 (bg) | Моно(2-амониев-2-хидроксиметил-1,3-пропандиол)(2r-сis)- (3-метоксиранил)фосфонат,получаване и фармацевтични състави,които го съдържат | |
| JPH0418015A (ja) | 安定なフマル酸クレマスチン水溶液 | |
| JPS61180771A (ja) | 安定な抗バクテリア剤水溶液 | |
| JPH0611704B2 (ja) | 角膜疾患治療用点眼剤 | |
| JPS61112010A (ja) | 安定な点眼剤 | |
| JP2005247804A (ja) | 点眼剤 | |
| US4377583A (en) | N-Methyl-D-glucamine salt of with 3,4-dihydro-5-methyl-6-(2-methylpropyl)-4-oxothieno[2,3-d]pyrimidine-2-carboxylic acid | |
| RU2176505C2 (ru) | Средство, обладающее противовирусной активностью, на основе соединений серебра и золота с тиазином и способ его получения | |
| US3322627A (en) | Method of treating herpes simplex infections with 5-methylamino-2'-deoxyuridine, and compositions therefor | |
| US2118133A (en) | Organic mercury compounds | |
| CA1217425A (fr) | Solutions d'oxytetracycline | |
| JPH0366617A (ja) | 静脈内投与用フエニトインナトリウム製剤 | |
| JPH06700B2 (ja) | 安定な水性液剤 |