KR850001693A - 아모술랄롤 하이드로클로라이드 지속성 제제의 제조방법 - Google Patents

아모술랄롤 하이드로클로라이드 지속성 제제의 제조방법 Download PDF

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KR850001693A
KR850001693A KR1019840005306A KR840005306A KR850001693A KR 850001693 A KR850001693 A KR 850001693A KR 1019840005306 A KR1019840005306 A KR 1019840005306A KR 840005306 A KR840005306 A KR 840005306A KR 850001693 A KR850001693 A KR 850001693A
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hydrochloride
mixture
enteric material
amosulolol
preparing
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KR1019840005306A
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KR910002670B1 (ko
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다까시(외 4) 소노베
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모리오까 시게오
야마노우치 팔마세티칼 코포레이션, 리미티드
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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
    • A61K9/20—Pills, tablets, discs, rods
    • 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
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1635—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • 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
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/18—Sulfonamides
    • 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
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1617—Organic compounds, e.g. phospholipids, fats
    • 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
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
    • 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
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2095—Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biophysics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Molecular Biology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Neurosurgery (AREA)
  • Cardiology (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

내용 없음

Description

아모술랄롤 하이드로클로라이드 지속성 제제의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 실시예 1에서 제조된 본 발명의 지속성 제제및 아모술랄롤 하이드로 클로라이드의 통상적인 제제를 경구투여할 때 단일-맹시험 교차 연구에 의한 시간에 따른 아모술랄롤 하이드로클로라이드의 혈장 수준을 나타낸다.
제2도는 실시예 2에서 제조된 본 발명의 지속성 제제 및 아모술랄롤 하이드로클로라이드의 통상적인 제제를 경구투여할때 단일-맹시험 교차연구에 의한 시간에 따른 아모술랄롤 하이드로클로라이드의 혈장 수준을 나타낸다. 비글종개 5마리의 평균치.
제3도는 실시예 3에서 제조된 본 발명의 지속성 제제 및 아모술랄롤 하이드로클로라이드의 수용액을 경구투여할때 단일-맹시험 교차연구에 의한 시간에 따른 아모술랄롤 하이드로 클로라이드의 혈장 수준을 나타낸다. 비글종개 6마리의 평균치.

Claims (5)

  1. 아모술랄롤 하이드로클로라이드 또는 아모술랄롤하이드로 클로라이드부형제의 혼합물에 장용성 물질 또는 물 또는 유기용매중 그의 용액 또는 현탁액을 가하고, 필요하다면 결합제를 사용하여 혼합물을 과립화시키고, 생성된 과립을 정제기로 타정함을 특징으로 하여 아모술랄롤 하이드로클로라이드 지속성 제제를 제조하는 방법.
  2. 제1항에 있어서, 장용성 물질이 메타크릴산 에틸 아크릴레이트 공중합체인 방법.
  3. 아모술랄롤 하이드로클로라이드 또는 아모술랄롤하이드로 클로라이드 및 부형제의 혼합물에 장용성 물질 또는 물 또는 유기용매중 그의 용액 또는 현탁액을 가하고, 장용성 물질의 첨가전 또는 후에 아모술랄롤 하이드로클로라이드 또는 아모술랄롤 하이드로 클로라이드와 부형제의 혼합물에 약제학적으로 무독한 유기산 또는 그의 용액을 가하고, 필요하다면, 결합제를 사용하여 이 혼합물을 과립화시키고, 생성된 과립을 정제기로 타정함을 특징으로 하여 아모술랄롤 하이드로클로라이드지속성 제제를 제조하는 방법.
  4. 제3항에 있어서, 장용성 물질이 메타크릴산·에틸-아크릴레이트 공중합체인 방법.
  5. 제3항에 있어서, 약제학적으로 무독한유기산이 시트르산 또는 타르타르 산인 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019840005306A 1983-08-31 1984-08-30 아모술랄롤 하이드로클로라이드 지속성 제제의 제조방법 KR910002670B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP160086 1983-08-31
JP58160086A JPS6051106A (ja) 1983-08-31 1983-08-31 塩酸アモスラロ−ル持続性製剤
JP58-160086 1983-08-31

Publications (2)

Publication Number Publication Date
KR850001693A true KR850001693A (ko) 1985-04-01
KR910002670B1 KR910002670B1 (ko) 1991-05-03

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KR1019840005306A KR910002670B1 (ko) 1983-08-31 1984-08-30 아모술랄롤 하이드로클로라이드 지속성 제제의 제조방법

Country Status (7)

Country Link
US (2) US4724148A (ko)
EP (1) EP0136103B1 (ko)
JP (1) JPS6051106A (ko)
KR (1) KR910002670B1 (ko)
AT (1) ATE57833T1 (ko)
DE (1) DE3483504D1 (ko)
ES (1) ES535545A0 (ko)

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Also Published As

Publication number Publication date
KR910002670B1 (ko) 1991-05-03
ATE57833T1 (de) 1990-11-15
EP0136103B1 (en) 1990-10-31
US4724148A (en) 1988-02-09
DE3483504D1 (de) 1990-12-06
EP0136103A3 (en) 1986-10-22
JPS6051106A (ja) 1985-03-22
ES8602406A1 (es) 1985-12-01
EP0136103A2 (en) 1985-04-03
US4765988A (en) 1988-08-23
ES535545A0 (es) 1985-12-01
JPH0443049B2 (ko) 1992-07-15

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