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不同透皮促进剂对环吡酮胺和水杨酸体外经皮渗透性的影响
引用本文:冯小龙,王晖,朱慧明.不同透皮促进剂对环吡酮胺和水杨酸体外经皮渗透性的影响[J].中国临床药理学与治疗学,2003,8(1):67-70.
作者姓名:冯小龙  王晖  朱慧明
作者单位:广东医学院药理教研室,湛江,524023,广东
基金项目:广东省教育厅资助项目 (GK0 10 3)
摘    要:目的:以环吡酮胺和水杨酸为模型药物。研究透皮促进剂对外用抗真菌药的促透特性。方法:在离体透皮实验装置上进行透皮吸收试验和贮库效应的研究。结果:1%氮酮和1%薄荷醇联用对环吡酮胺经皮渗透的促进作用明显高于其它组,1%的薄荷醇对水杨酸促透效果最佳。而由1%氮酮。2.5%丙二酮,2.5%油酸,1%薄荷醇合用对环吡酮胺的体外经皮渗透虽具有明显的促进作用和时滞明显缩短。但是与二联使用透皮促进剂比较并无明显优点。结论:薄荷醇和氮酮对环吡酮胺和水杨酸体外经皮吸收具有显的促进作用。两联用对脂溶性化合物环吡酮胺的促透作用更明显。

关 键 词:药理学  药物联用  离体透皮吸收试验  透皮促进剂  水杨酸  环吡酮胺  贮库效应
文章编号:1009-2501(2003)01-0067-04
修稿时间:2002年9月23日

Effects of different penetration enhancer on penetration of ciclopirox olamine and salysic acid in percutaneous penetration
FENG Xiao-Long,WANG Hui,ZHU Hui-Ming.Effects of different penetration enhancer on penetration of ciclopirox olamine and salysic acid in percutaneous penetration[J].Chinese Journal of Clinical Pharmacology and Therapeutics,2003,8(1):67-70.
Authors:FENG Xiao-Long  WANG Hui  ZHU Hui-Ming
Institution:FENG Xiao-Long,WANG Hui,ZHU Hui-Ming Department of Pharmacology,Guangdong Medical College,Zhanjiang 524023,Guangdong
Abstract:AIM: To study the enhancing effect of penetration enhancer on percutaneous absorption of antifungal agents. METHODS: Percutaneous penetration experiment was performed on device in vitro, and the deposit effects were observed with vivoperception. RESULTS: Combination of 1-menthol (1%) and azone (1%) showed the best effect on percutaneous absorption of cidopicox olamine, and 1-menthol (1%) had the best effect on percutaneous absorption of salysic acid. The compound penetration enhancer, consisting of 1-menthol (1%), azone (1%), propylene glycol ( 2.5%) and oleic acid ( 2.5%), had prominent action on absorption of cidopirox olamine through rabbit skins, and shorten the lag times obviously. CONCLUSION: L-menthol and azone can significantly enhance the percutaneous absorption of both salysic acid and cidopicox olamine. Combination of 1-menthol and azone can further increase the absorption.c
Keywords:pharmacology  salysic acid  ciclopirox olamine  percutaneous absorption  deposit effect
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