JPH0317809B2 - - Google Patents

Info

Publication number: JPH0317809B2
Authority: JP; Japan
Prior art keywords: weight; parts; chitosan; hydrochloride; drug
Prior art date: 1985-01-11
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

Application number

JP216085A

Other languages

English (en)

Japanese (ja)

Other versions

JPS61161216A (ja

Inventor

Juji Makino

Hideo Matsuki

Yoshiki Suzuki

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Teijin Ltd

Original Assignee

Teijin Ltd

Priority date (The priority date 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 date listed.)

1985-01-11

Filing date

1985-01-11

Publication date

1991-03-11

1985-01-11 Application filed by Teijin Ltd filed Critical Teijin Ltd

1985-01-11 Priority to JP216085A priority Critical patent/JPS61161216A/ja

1986-01-06 Priority to DE8686300039T priority patent/DE3686275T2/de

1986-01-06 Priority to EP86300039A priority patent/EP0187703B1/de

1986-01-10 Priority to US06/817,649 priority patent/US4814176A/en

1986-07-21 Publication of JPS61161216A publication Critical patent/JPS61161216A/ja

1991-03-11 Publication of JPH0317809B2 publication Critical patent/JPH0317809B2/ja

Status Granted legal-status Critical Current

Links

229920001661 Chitosan Polymers 0.000 claims description 41
239000003814 drug Substances 0.000 claims description 33
229940079593 drug Drugs 0.000 claims description 32
239000000203 mixture Substances 0.000 claims description 27
229920002125 Sokalan® Polymers 0.000 claims description 23
229920002101 Chitin Polymers 0.000 claims description 20
239000000843 powder Substances 0.000 claims description 15
238000013268 sustained release Methods 0.000 claims description 10
239000012730 sustained-release form Substances 0.000 claims description 10
239000008194 pharmaceutical composition Substances 0.000 claims description 9
239000008280 blood Substances 0.000 claims description 6
210000004369 blood Anatomy 0.000 claims description 6
239000008187 granular material Substances 0.000 claims description 4
239000003826 tablet Substances 0.000 claims description 2
CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 26
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 24
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
229960000905 indomethacin Drugs 0.000 description 13
235000019359 magnesium stearate Nutrition 0.000 description 12
238000000034 method Methods 0.000 description 11
-1 captryl Chemical compound 0.000 description 8
238000010828 elution Methods 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
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HYIMSNHJOBLJNT-UHFFFAOYSA-N nifedipine Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1C1=CC=CC=C1[N+]([O-])=O HYIMSNHJOBLJNT-UHFFFAOYSA-N 0.000 description 5
229960001597 nifedipine Drugs 0.000 description 5
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 4
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IMCGHZIGRANKHV-AJNGGQMLSA-N tert-butyl (3s,5s)-2-oxo-5-[(2s,4s)-5-oxo-4-propan-2-yloxolan-2-yl]-3-propan-2-ylpyrrolidine-1-carboxylate Chemical compound O1C(=O)[C@H](C(C)C)C[C@H]1[C@H]1N(C(=O)OC(C)(C)C)C(=O)[C@H](C(C)C)C1 IMCGHZIGRANKHV-AJNGGQMLSA-N 0.000 description 3
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229940124549 vasodilator Drugs 0.000 description 3
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MEAPRSDUXBHXGD-UHFFFAOYSA-N 3-chloro-n-(4-propan-2-ylphenyl)propanamide Chemical compound CC(C)C1=CC=C(NC(=O)CCCl)C=C1 MEAPRSDUXBHXGD-UHFFFAOYSA-N 0.000 description 2
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BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 2
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JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
238000001727 in vivo Methods 0.000 description 2
239000003589 local anesthetic agent Substances 0.000 description 2
229960005015 local anesthetics Drugs 0.000 description 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
239000002245 particle Substances 0.000 description 2
229960004604 propranolol hydrochloride Drugs 0.000 description 2
AQHHHDLHHXJYJD-UHFFFAOYSA-N propranolol hydrochloride Natural products C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 AQHHHDLHHXJYJD-UHFFFAOYSA-N 0.000 description 2
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UHSXRTHJCJGEKG-UQKRIMTDSA-N (1s)-1-[(3,4,5-trimethoxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinolin-2-ium-6,7-diol;chloride Chemical compound Cl.COC1=C(OC)C(OC)=CC(C[C@H]2C3=CC(O)=C(O)C=C3CCN2)=C1 UHSXRTHJCJGEKG-UQKRIMTDSA-N 0.000 description 1
YKFCISHFRZHKHY-NGQGLHOPSA-N (2s)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid;trihydrate Chemical compound O.O.O.OC(=O)[C@](N)(C)CC1=CC=C(O)C(O)=C1.OC(=O)[C@](N)(C)CC1=CC=C(O)C(O)=C1 YKFCISHFRZHKHY-NGQGLHOPSA-N 0.000 description 1
BGRJTUBHPOOWDU-NSHDSACASA-N (S)-(-)-sulpiride Chemical compound CCN1CCC[C@H]1CNC(=O)C1=CC(S(N)(=O)=O)=CC=C1OC BGRJTUBHPOOWDU-NSHDSACASA-N 0.000 description 1
FGOJCPKOOGIRPA-UHFFFAOYSA-N 1-o-tert-butyl 4-o-ethyl 5-oxoazepane-1,4-dicarboxylate Chemical compound CCOC(=O)C1CCN(C(=O)OC(C)(C)C)CCC1=O FGOJCPKOOGIRPA-UHFFFAOYSA-N 0.000 description 1
CIVCELMLGDGMKZ-UHFFFAOYSA-N 2,4-dichloro-6-methylpyridine-3-carboxylic acid Chemical compound CC1=CC(Cl)=C(C(O)=O)C(Cl)=N1 CIVCELMLGDGMKZ-UHFFFAOYSA-N 0.000 description 1
FEDJGPQLLNQAIY-UHFFFAOYSA-N 2-[(6-oxo-1h-pyridazin-3-yl)oxy]acetic acid Chemical compound OC(=O)COC=1C=CC(=O)NN=1 FEDJGPQLLNQAIY-UHFFFAOYSA-N 0.000 description 1
NKQVYJRZBVRXRU-UHFFFAOYSA-N 2-methyl-2-(methylamino)propanenitrile Chemical compound CNC(C)(C)C#N NKQVYJRZBVRXRU-UHFFFAOYSA-N 0.000 description 1
WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 1
UIAGMCDKSXEBJQ-IBGZPJMESA-N 3-o-(2-methoxyethyl) 5-o-propan-2-yl (4s)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate Chemical compound COCCOC(=O)C1=C(C)NC(C)=C(C(=O)OC(C)C)[C@H]1C1=CC=CC([N+]([O-])=O)=C1 UIAGMCDKSXEBJQ-IBGZPJMESA-N 0.000 description 1
WFJIVOKAWHGMBH-UHFFFAOYSA-N 4-hexylbenzene-1,3-diol Chemical compound CCCCCCC1=CC=C(O)C=C1O WFJIVOKAWHGMBH-UHFFFAOYSA-N 0.000 description 1
ROUDCKODIMKLNO-CTBSXBMHSA-N 6-oxoprostaglandin E1 Chemical compound CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1CC(=O)CCCCC(O)=O ROUDCKODIMKLNO-CTBSXBMHSA-N 0.000 description 1
IVVHAAOJLULJLK-YDXSIYMFSA-E Aceglutamide aluminum Chemical compound [OH-].[OH-].[OH-].[OH-].[Al+3].[Al+3].[Al+3].CC(=O)N[C@H](C([O-])=O)CCC(N)=O.CC(=O)N[C@H](C([O-])=O)CCC(N)=O.CC(=O)N[C@H](C([O-])=O)CCC(N)=O.CC(=O)N[C@H](C([O-])=O)CCC(N)=O.CC(=O)N[C@H](C([O-])=O)CCC(N)=O IVVHAAOJLULJLK-YDXSIYMFSA-E 0.000 description 1
241000416162 Astragalus gummifer Species 0.000 description 1
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AOCCBINRVIKJHY-UHFFFAOYSA-N Carmofur Chemical compound CCCCCCNC(=O)N1C=C(F)C(=O)NC1=O AOCCBINRVIKJHY-UHFFFAOYSA-N 0.000 description 1
WJLVQTJZDCGNJN-UHFFFAOYSA-N Chlorhexidine hydrochloride Chemical compound Cl.Cl.C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 WJLVQTJZDCGNJN-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
DBAKFASWICGISY-BTJKTKAUSA-N Chlorpheniramine maleate Chemical compound OC(=O)\C=C/C(O)=O.C=1C=CC=NC=1C(CCN(C)C)C1=CC=C(Cl)C=C1 DBAKFASWICGISY-BTJKTKAUSA-N 0.000 description 1
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KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
ZNIFSRGNXRYGHF-UHFFFAOYSA-N Clonidine hydrochloride Chemical compound Cl.ClC1=CC=CC(Cl)=C1NC1=NCCN1 ZNIFSRGNXRYGHF-UHFFFAOYSA-N 0.000 description 1
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FYBXRCFPOTXTJF-UHFFFAOYSA-N carteolol hydrochloride Chemical compound [Cl-].N1C(=O)CCC2=C1C=CC=C2OCC(O)C[NH2+]C(C)(C)C FYBXRCFPOTXTJF-UHFFFAOYSA-N 0.000 description 1
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229920000642 polymer Polymers 0.000 description 1
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235000019422 polyvinyl alcohol Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
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235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
229960003975 potassium Drugs 0.000 description 1
WFXFYZULCQKPIP-UHFFFAOYSA-N prazosin hydrochloride Chemical compound [H+].[Cl-].N=1C(N)=C2C=C(OC)C(OC)=CC2=NC=1N(CC1)CCN1C(=O)C1=CC=CO1 WFXFYZULCQKPIP-UHFFFAOYSA-N 0.000 description 1
229960002386 prazosin hydrochloride Drugs 0.000 description 1
229960005205 prednisolone Drugs 0.000 description 1
OIGNJSKKLXVSLS-VWUMJDOOSA-N prednisolone Chemical compound O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OIGNJSKKLXVSLS-VWUMJDOOSA-N 0.000 description 1
150000003180 prostaglandins Chemical class 0.000 description 1
238000010298 pulverizing process Methods 0.000 description 1
229950000112 serrapeptase Drugs 0.000 description 1
108010038132 serratiopeptidase Proteins 0.000 description 1
JGMJQSFLQWGYMQ-UHFFFAOYSA-M sodium;2,6-dichloro-n-phenylaniline;acetate Chemical compound [Na+].CC([O-])=O.ClC1=CC=CC(Cl)=C1NC1=CC=CC=C1 JGMJQSFLQWGYMQ-UHFFFAOYSA-M 0.000 description 1
210000003802 sputum Anatomy 0.000 description 1
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239000008117 stearic acid Substances 0.000 description 1
229960005202 streptokinase Drugs 0.000 description 1
MLKXDPUZXIRXEP-MFOYZWKCSA-N sulindac Chemical compound CC1=C(CC(O)=O)C2=CC(F)=CC=C2\C1=C/C1=CC=C(S(C)=O)C=C1 MLKXDPUZXIRXEP-MFOYZWKCSA-N 0.000 description 1
229960000894 sulindac Drugs 0.000 description 1
229960004940 sulpiride Drugs 0.000 description 1
238000013269 sustained drug release Methods 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
WFWLQNSHRPWKFK-ZCFIWIBFSA-N tegafur Chemical compound O=C1NC(=O)C(F)=CN1[C@@H]1OCCC1 WFWLQNSHRPWKFK-ZCFIWIBFSA-N 0.000 description 1
229960001674 tegafur Drugs 0.000 description 1
229960005105 terbutaline sulfate Drugs 0.000 description 1
KFVSLSTULZVNPG-UHFFFAOYSA-N terbutaline sulfate Chemical compound [O-]S([O-])(=O)=O.CC(C)(C)[NH2+]CC(O)C1=CC(O)=CC(O)=C1.CC(C)(C)[NH2+]CC(O)C1=CC(O)=CC(O)=C1 KFVSLSTULZVNPG-UHFFFAOYSA-N 0.000 description 1
WUBVEMGCQRSBBT-UHFFFAOYSA-N tert-butyl 4-(trifluoromethylsulfonyloxy)-3,6-dihydro-2h-pyridine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(OS(=O)(=O)C(F)(F)F)=CC1 WUBVEMGCQRSBBT-UHFFFAOYSA-N 0.000 description 1
229950010302 tiaramide Drugs 0.000 description 1
HTJXMOGUGMSZOG-UHFFFAOYSA-N tiaramide Chemical compound C1CN(CCO)CCN1C(=O)CN1C(=O)SC2=CC=C(Cl)C=C21 HTJXMOGUGMSZOG-UHFFFAOYSA-N 0.000 description 1
229950009883 tocopheryl nicotinate Drugs 0.000 description 1
238000011200 topical administration Methods 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
NZHGWWWHIYHZNX-CSKARUKUSA-N tranilast Chemical compound C1=C(OC)C(OC)=CC=C1\C=C\C(=O)NC1=CC=CC=C1C(O)=O NZHGWWWHIYHZNX-CSKARUKUSA-N 0.000 description 1
229960005342 tranilast Drugs 0.000 description 1
229960000363 trapidil Drugs 0.000 description 1
229960005294 triamcinolone Drugs 0.000 description 1
GFNANZIMVAIWHM-OBYCQNJPSA-N triamcinolone Chemical compound O=C1C=C[C@]2(C)[C@@]3(F)[C@@H](O)C[C@](C)([C@@]([C@H](O)C4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 GFNANZIMVAIWHM-OBYCQNJPSA-N 0.000 description 1
229960002117 triamcinolone acetonide Drugs 0.000 description 1
YNDXUCZADRHECN-JNQJZLCISA-N triamcinolone acetonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O YNDXUCZADRHECN-JNQJZLCISA-N 0.000 description 1
229960001177 trimetazidine Drugs 0.000 description 1
210000003462 vein Anatomy 0.000 description 1
229960000881 verapamil hydrochloride Drugs 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
238000005303 weighing Methods 0.000 description 1
UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1

Landscapes

Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicinal Preparation (AREA)

JP216085A 1985-01-11 1985-01-11 キトサン類を用いた徐放性医薬品組成物 Granted JPS61161216A (ja)

Priority Applications (4)

Application Number	Priority Date	Filing Date	Title
JP216085A JPS61161216A (ja)	1985-01-11	1985-01-11	キトサン類を用いた徐放性医薬品組成物
DE8686300039T DE3686275T2 (de)	1985-01-11	1986-01-06	Praeparate mit verzoegerter freisetzung.
EP86300039A EP0187703B1 (de)	1985-01-11	1986-01-06	Präparate mit verzögerter Freisetzung
US06/817,649 US4814176A (en)	1985-01-11	1986-01-10	Sustained release preparation

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP216085A JPS61161216A (ja)	1985-01-11	1985-01-11	キトサン類を用いた徐放性医薬品組成物

Publications (2)

Publication Number	Publication Date
JPS61161216A JPS61161216A (ja)	1986-07-21
JPH0317809B2 true JPH0317809B2 (de)	1991-03-11

Family

ID=11521601

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP216085A Granted JPS61161216A (ja)	1985-01-11	1985-01-11	キトサン類を用いた徐放性医薬品組成物

Country Status (1)

Country	Link
JP (1)	JPS61161216A (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1586313A1 (de) *	2004-04-07	2005-10-19	The Jordanian Pharmaceutical Manufacturing Co. Ltd.	Metoclopramid enthaltende pharmazeutische Zubereitungen und Herstellungsmethode
ITME20040015A1 (it) *	2004-12-07	2005-03-07	Vincenzo Savica	Chewing gum, caramelle gommose, pastiglie, compresse a lento rilascio di chelanti fosfato e/o fosforo salivare e capsule a lento rilascio di chelanti fosfato e/o fosforo a livello gastroenterico.

1985
- 1985-01-11 JP JP216085A patent/JPS61161216A/ja active Granted

Also Published As

Publication number	Publication date
JPS61161216A (ja)	1986-07-21

Legal Events

Date	Code	Title	Description
2004-03-11	LAPS	Cancellation because of no payment of annual fees

Publication	Publication Date	Title
JP2916152B2 (ja)	1999-07-05	薬物放出速度調節型製剤
DE3686275T2 (de)	1993-03-18	Praeparate mit verzoegerter freisetzung.
US4834985A (en)	1989-05-30	Controlled release pharmaceutical composition
JP4077886B2 (ja)	2008-04-23	不溶性薬剤の持効性ヘテロ分散ヒドロゲル系
KR100384215B1 (ko)	2003-08-30	방출지속성다분산하디로겔시스템-비정질약물
AU595801B2 (en)	1990-04-12	Oral pharmaceutical composition
US6217903B1 (en)	2001-04-17	Sustained release polymer blend for pharmaceutical applications
KR100355130B1 (ko)	2003-01-30	하이드로겔서방성정제
US5451409A (en)	1995-09-19	Sustained release matrix system using hydroxyethyl cellulose and hydroxypropyl cellulose polymer blends
US4695591A (en)	1987-09-22	Controlled release dosage forms comprising hydroxypropylmethylcellulose
EP0231826B1 (de)	1991-12-04	Theophyllintablette mit verzögerter Freigabe
JPH06172221A (ja)	1994-06-21	多相解放特性を有する凝集親水性錯体
JPS63258407A (ja)	1988-10-25	徐放性カプセル
SE453796B (sv)	1988-03-07	Fast, terapeutisk komposition vars berarbasmaterial utgores av hydroxypropylmetylcellulosa samt ev natriumkarboximetylcellulosa
JPWO1994006414A1 (ja)	1994-10-06	ハイドロゲル徐放性製剤
EP0227814A1 (de)	1987-07-08	Therapeutische zusammensetzungen mit bimodalabgabe-charakteristiken
EP0207638A2 (de)	1987-01-07	Arzneizubereitung mit verzögerter Wirkstoffabgabe
KR20090119993A (ko)	2009-11-23	구강내 붕괴정
US20060088594A1 (en)	2006-04-27	Highly compressible controlled delivery compositions of metformin
JPS62120315A (ja)	1987-06-01	経口投与型徐放性錠剤の製造方法
WO2007123021A1 (ja)	2007-11-01	徐放性錠剤の製造方法
MX2007005427A (es)	2012-10-02	Composicion de dispersion solida de pranlukast con biodisponibilidad mejorada y metodo para preparar la dispersion solida.
JPS6344125B2 (de)	1988-09-02
JP3598049B2 (ja)	2004-12-08	ハイドロゲル徐放性製剤
JPH0317809B2 (de)	1991-03-11