JPS60224632A - External drug for treating dermatopathy - Google Patents
External drug for treating dermatopathyInfo
- Publication number
- JPS60224632A JPS60224632A JP59082476A JP8247684A JPS60224632A JP S60224632 A JPS60224632 A JP S60224632A JP 59082476 A JP59082476 A JP 59082476A JP 8247684 A JP8247684 A JP 8247684A JP S60224632 A JPS60224632 A JP S60224632A
- Authority
- JP
- Japan
- Prior art keywords
- kallikrein
- ointment
- base
- external drug
- dermatopathy
- 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.)
- Pending
Links
Landscapes
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はカリクレインを含有して成る皮膚疾患治療用外
用剤に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an external preparation for treating skin diseases containing kallikrein.
カリクレインは膵臓から分泌される物質で、血漿蛋白か
らキニンを遊離させ血圧降下作用を惹起させる酵素であ
る□本品は、始めイヌの砕臓から抽出されたが、その後
ヒトを含む種々の動物の体液や組織からも同様のものが
得られている。Kallikrein is a substance secreted by the pancreas, and is an enzyme that releases kinin from plasma proteins and induces a blood pressure-lowering effect. This product was first extracted from crushed dog viscera, but has since been extracted from various animals including humans. Similar substances are obtained from body fluids and tissues.
17いf1978年に到りブタ膵臓由来カリクレインの
全アミノ駿配列が決定され、一方その薬理作用も詳JI
K検討されたO
すなわちカリクレインは血液中のキニノーゲンを分解し
。In 1978, the entire amino acid sequence of kallikrein derived from pig pancreas was determined, and its pharmacological effects were also detailed in JI.
K studied O That is, kallikrein breaks down kininogen in the blood.
こ\に遊離したカリジンは、神経を介せず直接に血管の
平滑筋に作用して末梢血管の拡張、血管抵抗の減少、血
流増加及び血圧降下などの作用を呈することが、イヌを
用いての薬理実験によって確められた。Using dogs, it was shown that the liberated kallidin acts directly on vascular smooth muscle without going through nerves, dilating peripheral blood vessels, decreasing vascular resistance, increasing blood flow, and lowering blood pressure. This was confirmed by several pharmacological experiments.
今日ではカリクレインは血管拡張剤として広く用いられ
ており、脳動脈硬化症、高血圧症及び血行障害自乗の組
織営養障害に有効とされている。Today, kallikrein is widely used as a vasodilator and is said to be effective for cerebral arteriosclerosis, hypertension, and tissue malnutrition caused by blood circulation disorders.
しかし、現在市販ずれているカリクレイン製剤はすべて
錠剤及び注射剤の形態で使用され、外用剤は全く見られ
ない。However, all kallikrein preparations currently on the market are used in the form of tablets and injections, and there are no external preparations available.
その理由はカリクレインが水に対して不安定であること
の他。The reason for this is that kallikrein is unstable in water.
カリクレインの皮膚疾患に対する研究が進んでいなかり
たことKもよる。This is also due to the fact that research into kallikrein for skin diseases has not progressed.
本発明者は新しい剤型によるカリクレインの新用途を開
発すべく徨々研究を重ねたところ、カリクレインの軟膏
基剤との親和性が高いこと、更1cFi得られたカリク
レイン軟膏は皮膚疾患の治療忙好適であることを見出し
て本発明を完成したものである。The present inventor conducted extensive research to develop a new use for kallikrein using a new dosage form, and found that kallikrein has a high affinity with the ointment base, and that kallikrein ointment, which has a 1 cFi content, is currently used in the treatment of skin diseases. The present invention was completed by discovering that this is suitable.
本発明において#−を種々の動物の体液や臓器に由来す
るカリクレインを用いることができるが、ブタ膵臓由来
の4のは入手も容易であるので1通常はこれを用いるの
が好ましい。In the present invention, kallikrein derived from body fluids and organs of various animals can be used for #-, but it is usually preferable to use #4 derived from pig pancreas because it is easily available.
本発明においてはこれらのカリクレインを軟膏基剤に配
合する。使用できる基剤としては1例えば日本薬局方の
吸水軟膏、白色軟膏、親水軟膏、単軟膏、親水ワセリン
はむろん。In the present invention, these kallikrein are blended into an ointment base. Examples of bases that can be used include, for example, water-absorbing ointment, white ointment, hydrophilic ointment, simple ointment, and hydrophilic petrolatum of the Japanese Pharmacopoeia.
これ以外の通常の軟膏基剤はすべて適宜使用できる。All other conventional ointment bases may be used as appropriate.
カリクレインと基剤との配合は両者な単に練合するのみ
で良く、必要に応じプロピレングリコールやポリエチレ
ングリコールに溶解したのち基剤VclIIり込むのも
有利である。基剤に対するこれらの有機溶媒の比率は任
意で良いが好ましくけ2〜10チ更1ctH1I、<は
4チ前後である。このようKして本発明の皮膚疾患治療
用外用剤が製造できる。その中のカリクレイン含量は任
意であるが好ましくは1〜100力リクレイン単位/
g、 4Iに好オしくは10〜30力リクレイン単位/
gである。Kallikrein and the base may be blended by simply kneading the two, and if necessary, it is also advantageous to dissolve the kallikrein in propylene glycol or polyethylene glycol and then incorporate it into the base VclII. The ratio of these organic solvents to the base may be arbitrary, but is preferably 2 to 10 ctH1I, and <= about 4 ctH1I. In this manner, the external preparation for treating skin diseases of the present invention can be produced. The kallikrein content therein is arbitrary, but preferably 1 to 100 kallikrein units/
g, preferably 10 to 30 force recline units/4I
It is g.
上記のよう和して得られた本発明のカリクレイン含有外
用剤Fi、これを種々の皮膚疾患に用いたところ1次の
ように優れた効果を示した。When the kallikrein-containing external preparation Fi of the present invention obtained by the above-mentioned combination was used for various skin diseases, it showed the following excellent effects.
以上に詳細に説明したように本発明のカリクレイン含有
外用剤は、未だかって用いられたことのない新しい剤型
であり。As explained in detail above, the kallikrein-containing external preparation of the present invention is a new dosage form that has never been used before.
しかもこ\に得られたカリクレイン復側は未だかって何
人も試みなかった皮膚疾患の領域に適用して著しい治療
効果を示すものであり、従って本発明は正に新規かつ有
用な発明というべきである。Moreover, the Kallikrein recovery agent thus obtained shows a remarkable therapeutic effect when applied to areas of skin diseases that no one has tried before.Therefore, the present invention can be truly called a novel and useful invention. .
以下参考までに本発明の外用剤の製法の一例を示す。む
ろんこれは単に参考のために例示したものであって9本
発明がこれKよって限定されるものでVi々い。An example of the method for producing the external preparation of the present invention is shown below for reference. Of course, this is merely an example for reference, and the present invention is not limited thereby.
精製ブタ肝臓由来カリクレインをとりこれを適量のプロ
ピレングリコールに溶解し1次いで日本薬局方の親水ワ
セリン中へ上記の溶液が4% (v/w)Kなるように
添加しよく練合し、カリクレイン濃度が27力リクレイ
ン単位/gとなるようIcv4節し、目的とするクリー
ム様の軟膏製剤を得る。Take purified pig liver-derived kallikrein, dissolve it in an appropriate amount of propylene glycol, then add the above solution to hydrophilic petrolatum of the Japanese Pharmacopoeia so that the concentration is 4% (v/w) K, and mix thoroughly to determine the kallikrein concentration. The Icv was adjusted to 4 to give a concentration of 27 Recrein units/g to obtain the desired cream-like ointment preparation.
以上
特許出願人 内 藤 俊 −
手続補正書(方式)
1、事件の表示 特願昭59−82476号2、発明の
名称 皮膚疾患治療用外用剤3、補正をする者
事件との関係 特許出願人
住所 京都市山科区北花山河原町37?I¥地の7昭和
59年7月31日(発送日)
5、補正の対象
願書及び明細書
6、補正の内容
添付のとおりPatent applicant Shun Naito - Procedural amendment (method) 1. Indication of the case Japanese Patent Application No. 59-82476 2. Title of the invention External preparation for the treatment of skin diseases 3. Relationship with the person making the amendment Patent applicant Address: 37 Kitakayama Kawaramachi, Yamashina-ku, Kyoto City? 7 July 31, 1982 (shipping date) 5. Application subject to amendment and specification 6. Contents of amendment as attached.
Claims (1)
2、カリクレインと軟膏基剤とから成る第1項記載の皮
膚疾患治療用外用剤 3、皮膚疾患がアカギン1手の荒れ、皮膚炎、壊死性血
管炎。 しもやけ及び褥廣である第1項記載の皮膚疾患治療用外
用剤[Scope of Claims] 1. External preparation for treating skin diseases comprising kallikrein 2. External preparation for treating skin diseases according to claim 1 comprising kallikrein and an ointment base 3. Roughness, dermatitis, necrotizing vasculitis. External preparation for treating the skin disease described in item 1, which is chilblains and bedsores.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59082476A JPS60224632A (en) | 1984-04-24 | 1984-04-24 | External drug for treating dermatopathy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59082476A JPS60224632A (en) | 1984-04-24 | 1984-04-24 | External drug for treating dermatopathy |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60224632A true JPS60224632A (en) | 1985-11-09 |
Family
ID=13775564
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59082476A Pending JPS60224632A (en) | 1984-04-24 | 1984-04-24 | External drug for treating dermatopathy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60224632A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0546533A2 (en) * | 1991-12-10 | 1993-06-16 | Sanwa Kagaku Kenkyusho Co., Ltd. | Medical use of kininogenase |
JPH05163158A (en) * | 1991-12-13 | 1993-06-29 | Sanwa Kagaku Kenkyusho Co Ltd | Agent for prevention and treatment of skin sore containing human urinary kininogenase as active component |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55104206A (en) * | 1979-02-05 | 1980-08-09 | Rooman Kogyo:Kk | Cosmetic containing enzyme |
JPS5798214A (en) * | 1980-12-10 | 1982-06-18 | Green Cross Corp:The | Recovery of kallikrein from human urine |
-
1984
- 1984-04-24 JP JP59082476A patent/JPS60224632A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55104206A (en) * | 1979-02-05 | 1980-08-09 | Rooman Kogyo:Kk | Cosmetic containing enzyme |
JPS5798214A (en) * | 1980-12-10 | 1982-06-18 | Green Cross Corp:The | Recovery of kallikrein from human urine |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0546533A2 (en) * | 1991-12-10 | 1993-06-16 | Sanwa Kagaku Kenkyusho Co., Ltd. | Medical use of kininogenase |
EP0546533A3 (en) * | 1991-12-10 | 1994-03-30 | Sanwa Kagaku Kenkyusho Co | |
JPH05163158A (en) * | 1991-12-13 | 1993-06-29 | Sanwa Kagaku Kenkyusho Co Ltd | Agent for prevention and treatment of skin sore containing human urinary kininogenase as active component |
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