KR950028772A - Indomethacin external preparation and its manufacturing method - Google Patents

Indomethacin external preparation and its manufacturing method Download PDF

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Publication number
KR950028772A
KR950028772A KR1019940009330A KR19940009330A KR950028772A KR 950028772 A KR950028772 A KR 950028772A KR 1019940009330 A KR1019940009330 A KR 1019940009330A KR 19940009330 A KR19940009330 A KR 19940009330A KR 950028772 A KR950028772 A KR 950028772A
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KR
South Korea
Prior art keywords
indomethacin
poloxamer
lower alcohols
purified water
tocopherol acetate
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KR1019940009330A
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Korean (ko)
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KR0142900B1 (en
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김운장
이한구
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김운장
대화제약 주식회사
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Priority to KR1019940009330A priority Critical patent/KR0142900B1/en
Publication of KR950028772A publication Critical patent/KR950028772A/en
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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
    • A61K9/06—Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Inorganic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

본 발명은 활성성분으로서 인도메타신을 함유하는 새로운 인도메타신 외용제제 및 그 제조방법에 관한 것으로, 겔화기제로서 폴록사머 유도체를 함유하여 피부의 자극을 최소화하며, 약물의 피부 투과율을 높인 새로운 인도메타신 겔제제를 제공한다.The present invention relates to a new indomethacin external preparation containing indomethacin as an active ingredient and a method for preparing the same, and a new indomethac which contains poloxamer derivatives as a gelling agent to minimize skin irritation and increases skin permeability of drugs. Provide a sour gel formulation.

본 발명은 또한 인도메타신과 폴록사머 유도체를 가열, 용융시키고, 따로 저급알코올류에 용해가능한 성분을 용해시켜 상기 용융액에 가하고, 여기에 수용성 물질을 녹인 정제수 또는 완충액을 추가로 가하여 인도메타신겔제제를 제조하는 방법을 제공한다.The present invention also heats and melts indomethacin and poloxamer derivatives, and separately dissolves soluble components in lower alcohols, adds to the melt, and further adds purified water or a buffer in which water-soluble substances are added to indomethacin gel formulation. It provides a method of manufacturing.

Description

인도메타신 외용제제 및 그 제조방법Indomethacin external preparation and its manufacturing method

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

제1도는 PH에 따른 본 발명의 겔제제의 피부 투과율을 나타내는 그래프이다.1 is a graph showing the skin permeability of the gel preparation of the present invention according to PH.

Claims (8)

활성성분으로서 인도메타신; 및 폴록사머 407; 저급알코올류; 토코페롤 아세테이트 0-2.0%; 멘톨오일 0-0.1%; 통상의 보조제와 정제수 또는 완충액을 균질하게 혼합시켜서 제조된 인도메타신 겔제제.Indomethacin as active ingredient; And poloxamer 407; Lower alcohols; Tocopherol acetate 0-2.0%; Menthol oil 0-0.1%; An indomethacin gel preparation prepared by homogeneously mixing a conventional adjuvant with purified water or a buffer solution. 제1항에서, 인도메타신 0.1-3.0%; 폴록사머 407 20.0-30.0%;저급알코올류 5.0-20.0%;토코페롤 아세테이트 0-2.0%; 멘톨오일 0-1.0%를 함유하는 인도메타신 겔제제.The method of claim 1, wherein indomethacin 0.1-3.0%; Poloxamer 407 20.0-30.0%; lower alcohols 5.0-20.0%; tocopherol acetate 0-2.0%; Indomethacin gel formulation containing 0-1.0% of menthol oil. 제1항 또는 제2항에서, 용해보조제로 프로필렌글리콜 또는 폴리에틸렌글리콜류에서 선택된 용해보조제 5.0-20.0%를 함유하는 인도메타신 겔제제.The indomethacin gel preparation according to claim 1 or 2, comprising 5.0-20.0% of a dissolution aid selected from propylene glycol or polyethylene glycol as a dissolution aid. 제1항 또는 제2항에서, 인도메타신 0.1-3.0%, 폴록사머 407 20.0-30.0%, 저급알코올류 5.0-20.0%, 프로필렌글리콜 또는 폴리에틸렌글리콜류에서 선택된 용해보조제 5.0-20.0%, 염화나트륨 0.1-1.0%, 토고페롤 아세테이트 0-2.0%, 멘톨오일 0-1.0%를 함유하는 인도메타신 겔제제.The dissolving aid according to claim 1 or 2 selected from indomethacin 0.1-3.0%, poloxamer 407 20.0-30.0%, lower alcohols 5.0-20.0%, propylene glycol or polyethylene glycols, sodium chloride 0.1 Indomethacin gel formulation containing -1.0%, togoferol acetate 0-2.0%, menthol oil 0-1.0%. 인도메타신과 폴록사머 407을 가열, 용융시키고, 여기에 토코페롤 아세테이트 0-2.0% 및 멘톨오일 0-1.0%를 녹인 저급알코올류를 가하고, 다시 정제수 또는 완충액을 가하여 균질하게 혼합시켜서 인도메타신 겔제제를 제조하는 방법.Indomethacin and poloxamer 407 were heated and melted, and low alcohols dissolved in 0-2.0% of tocopherol acetate and 0-1.0% of menthol oil were added thereto, followed by further mixing with purified water or buffer solution to form indomethacin gel. How to prepare. 제5항에서, 인도메타신 0.1-3.0%; 폴록사머 407 20.0-30.0%; 저급알코올류 5.0-20.0%; 토코페롤 아세테이트 0-2.0%; 멘톨오일 0-1.0%;를 함유하는 인도메타신 겔제제를 제조하는 방법.The method of claim 5, wherein indomethacin 0.1-3.0%; Poloxamer 407 20.0-30.0%; Lower alcohols 5.0-20.0%; Tocopherol acetate 0-2.0%; Indomethacin gel preparation containing menthol oil 0-1.0%. 제5항 또는 제6항에서, 폴리에틸렌글리콜류 5.0-20.0%, 염화나트륨 0.1-1.0%에서 선택된 1종 이상의 물질을 정제수 또는 완충액에 용해시켜 가한 인도메타신 겔제제를 제조하는 방법.The method for preparing indomethacin gel preparation according to claim 5 or 6, wherein one or more substances selected from 5.0-20.0% polyethylene glycol and 0.1-1.0% sodium chloride are dissolved in purified water or a buffer solution. 제5항 또는 제6항에서, 인도메타신 0.1-3.0%과 폴록사머 407 20.0-30.0%를 가열, 용융시키고, 따로 저급알코올류 5.0-20.0%에 프로필렌글리콜 5.0-20.0%, 토코페롤 아세테이트 0-2.0%, 멘톨오일 0-1.0%에서 선택된 1종 이상의 물질을 용해시켜 가하고, 염화나트륨 0.1-1.0%, 폴리에틸렌글리콜 5.0-20.0%(단, 프로필렌글리콜이 선택되지 않은 경우 선택될 수 있다)에서 선택된 1종 이상의 물질을 정제수 또는 완충액에 용해시켜 가한 인도메타신 겔제제를 제조하는 방법.The method according to claim 5 or 6, 0.1-3.0% indomethacin and 20.0-30.0% poloxamer 407 is heated and melted separately, 5.0-20.0% lower alcohols 5.0-20.0% propylene glycol 5.0-20.0%, tocopherol acetate 0- 1% or more selected by dissolving 2.0%, menthol oil 0-1.0% and adding 1, selected from sodium chloride 0.1-1.0%, polyethylene glycol 5.0-20.0% (if propylene glycol is not selected) A method for preparing an indomethacin gel preparation by dissolving more than one substance in purified water or a buffer. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019940009330A 1994-04-29 1994-04-29 Indomethacin external preparation KR0142900B1 (en)

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Application Number Priority Date Filing Date Title
KR1019940009330A KR0142900B1 (en) 1994-04-29 1994-04-29 Indomethacin external preparation

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KR950028772A true KR950028772A (en) 1995-11-22
KR0142900B1 KR0142900B1 (en) 1998-07-15

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112294750A (en) * 2020-10-29 2021-02-02 广东药科大学 Indometacin micelle composite microneedle and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112294750A (en) * 2020-10-29 2021-02-02 广东药科大学 Indometacin micelle composite microneedle and preparation method thereof
CN112294750B (en) * 2020-10-29 2023-06-20 广东药科大学 Indometate Xin Jiaoshu composite microneedle and preparation method thereof

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