KR850002399A - 액체 서방출성 제형의 제조방법 - Google Patents

액체 서방출성 제형의 제조방법 Download PDF

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Publication number
KR850002399A
KR850002399A KR1019840005637A KR840005637A KR850002399A KR 850002399 A KR850002399 A KR 850002399A KR 1019840005637 A KR1019840005637 A KR 1019840005637A KR 840005637 A KR840005637 A KR 840005637A KR 850002399 A KR850002399 A KR 850002399A
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KR
South Korea
Prior art keywords
drug
sustained release
release formulation
chlorpheniramine
preparing liquid
Prior art date
Application number
KR1019840005637A
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English (en)
Other versions
KR910003557B1 (ko
Inventor
엘. 슈메이커 제리
Original Assignee
베라 엠. 바이른
펜왈트 코포레이션
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.)
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Publication date
Application filed by 베라 엠. 바이른, 펜왈트 코포레이션 filed Critical 베라 엠. 바이른
Publication of KR850002399A publication Critical patent/KR850002399A/ko
Application granted granted Critical
Publication of KR910003557B1 publication Critical patent/KR910003557B1/ko

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0087Galenical forms not covered by A61K9/02 - A61K9/7023
    • A61K9/0095Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/56Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
    • A61K47/58Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. poly[meth]acrylate, polyacrylamide, polystyrene, polyvinylpyrrolidone, polyvinylalcohol or polystyrene sulfonic acid resin
    • A61K47/585Ion exchange resins, e.g. polystyrene sulfonic acid resin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/5084Mixtures of one or more drugs in different galenical forms, at least one of which being granules, microcapsules or (coated) microparticles according to A61K9/16 or A61K9/50, e.g. for obtaining a specific release pattern or for combining different drugs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Dispersion Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicinal Preparation (AREA)
  • Steroid Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

내용 없음

Description

액체 서방출성 제형의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (7)

  1. 제1약물의 피복, 약물-수지 복합체의 액체현탁제를 생성시키고, 별도의 용기에 제2약물의 비피복, 불용성 약물-수지 복합체의 액체현탁제를 생성시킨 다음이 둘의 액체 현탁제를 혼합시킴을 특징으로 하여, 액체담체중에 현탁된 피복, 약물-수지 복합체로서 존재하는 이온성인 한가지 이상의 제 1약물 및 제1 약물과 동일한 전하를 띄고 비피복, 이온성인 한가지 이상의 제 2약물로 이루어진 이온적으로 안정한 서방출성 제형을 제조하는 방법.
  2. 제1항에 있어서, 제1 약물이 코데인인 방법.
  3. 제2항에 있어서, 제2 약물이 클로르페니라민인 방법.
  4. 제1항에 있어서, 제1 약물이 슈도에페드린인 방법.
  5. 제4항에 있어서, 제2 약물이 클로르페니라민인 방법.
  6. 제1항에 있어서, 제1 약물이 하이드로코돈인 방법.
  7. 제6항에 있어서, 제2 약물이 클로르페니라민인 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019840005637A 1983-09-16 1984-09-15 액체 서방성 약물 제형의 제조방법 KR910003557B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US53286483A 1983-09-16 1983-09-16
US532,864 1983-09-16
US532864 1983-09-16

Publications (2)

Publication Number Publication Date
KR850002399A true KR850002399A (ko) 1985-05-13
KR910003557B1 KR910003557B1 (ko) 1991-06-05

Family

ID=24123487

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019840005637A KR910003557B1 (ko) 1983-09-16 1984-09-15 액체 서방성 약물 제형의 제조방법

Country Status (16)

Country Link
EP (1) EP0139881B1 (ko)
JP (1) JPH0688901B2 (ko)
KR (1) KR910003557B1 (ko)
AT (1) ATE42894T1 (ko)
AU (1) AU565487B2 (ko)
CA (1) CA1221632A (ko)
DE (1) DE3478085D1 (ko)
DK (1) DK164019C (ko)
FI (1) FI843609L (ko)
IE (1) IE57445B1 (ko)
IL (1) IL71886A (ko)
MX (1) MX171030B (ko)
NO (1) NO843673L (ko)
NZ (1) NZ208155A (ko)
PH (1) PH20237A (ko)
ZA (1) ZA844023B (ko)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4692462A (en) * 1985-03-18 1987-09-08 Menley & James Laboratories, Ltd. Compositions and method of controlling transdermal penetration of topical and systemic agents
CA1331563C (en) * 1987-08-03 1994-08-23 Gaylen M. Zentner Device for the controlled release of drugs with donnan-like modulation by charged insoluble resins
US4853229A (en) * 1987-10-26 1989-08-01 Alza Corporation Method for adminstering tiny pills
US5186930A (en) * 1988-11-14 1993-02-16 Schering Corporation Sustained release oral suspensions
US4999189A (en) * 1988-11-14 1991-03-12 Schering Corporation Sustained release oral suspensions
SE9103110D0 (sv) 1991-10-24 1991-10-24 Kabi Pharmacia Ab New drug formulation
GB2360894B (en) * 2000-03-30 2004-11-10 Peter Thomas Bosson Display device support system
WO2008151071A1 (en) * 2007-05-30 2008-12-11 Neos Therapeutics, Lp Modifying drug release in suspensions of ionic resin systems
US20150056288A1 (en) 2011-12-14 2015-02-26 Wockhardt Limited Modified release liquid pharmaceutical composition comprising bromopheniramine, pseudoephedrine and dextromethorphan

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2990332A (en) * 1958-04-02 1961-06-27 Wallace & Tiernan Inc Pharmaceutical preparations comprising cation exchange resin adsorption compounds and treatment therewith
US3138525A (en) * 1961-06-16 1964-06-23 Hoffmann La Roche Castor wax-amprotropine-resin compositions
FR5227M (ko) * 1966-03-18 1967-08-14
DE2246037B2 (de) * 1972-09-20 1975-02-27 Taeschner & Co, 8831 Kipfenberg Peroral anwendbares Arzneimittel mit verzögerter Resorbierbarkeit in Suspensionsform
US4221778A (en) * 1979-01-08 1980-09-09 Pennwalt Corporation Prolonged release pharmaceutical preparations

Also Published As

Publication number Publication date
IL71886A (en) 1987-11-30
FI843609A0 (fi) 1984-09-14
NZ208155A (en) 1987-09-30
DK434784D0 (da) 1984-09-12
IE57445B1 (en) 1992-09-09
JPS6067418A (ja) 1985-04-17
CA1221632A (en) 1987-05-12
DK434784A (da) 1985-03-17
FI843609L (fi) 1985-03-17
DE3478085D1 (en) 1989-06-15
EP0139881B1 (en) 1989-05-10
KR910003557B1 (ko) 1991-06-05
PH20237A (en) 1986-11-10
ATE42894T1 (de) 1989-05-15
AU2789184A (en) 1985-03-21
NO843673L (no) 1985-03-18
EP0139881A1 (en) 1985-05-08
AU565487B2 (en) 1987-09-17
DK164019B (da) 1992-05-04
JPH0688901B2 (ja) 1994-11-09
DK164019C (da) 1992-09-28
ZA844023B (en) 1985-03-27
IE841201L (en) 1985-03-16
IL71886A0 (en) 1984-09-30
MX171030B (es) 1993-09-27

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