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渗透促进剂对硝苯地平经皮吸收的影响。避蚊胺与氮酮的比较。

Effects of penetration enhancers on percutaneous absorption of nifedipine. Comparison between Deet and Azone.

作者信息

Kondo S, Mizuno T, Sugimoto I

机构信息

Pharmaceuticals Research Center, Kanebo, Ltd., Osaka, Japan.

出版信息

J Pharmacobiodyn. 1988 Feb;11(2):88-94. doi: 10.1248/bpb1978.11.88.

Abstract

The influence of N, N-diethyl-m-toluamide (Deet) and 1-dodecylazacycloheptan-2-one (Azone), on skin permeability was examined for nifedipine (NP), taking into account their effects on the thermodynamic activity of the drug. The percutaneous absorption efficiency of NP was determined by measuring the drug concentration in rat plasma. Comparisons were made among NP suspensions in the enhancers to ensure equal thermodynamic activity. Azone increased NP penetration over that of propylene glycol (PG), while Deet produced a similar response to that of PG. The addition of a small amount of Deet to PG or diethyl sebacate (DES) provided for a rather large increase in NP penetration compared with that from PG or DES alone. The results of this study strongly suggest that Deet and Azone have different modes of action. Azone exerted a genuine effect on the skin and produced marked improvement in the penetration of NP. The effect of Deet was interesting as it was effective only in combination with other vehicles. Deet exhibits excellent solubilizing properties and penetrates the skin easily. Accordingly, it may be concluded that Deet functions simply as a cosolvent to produce saturated or supersaturated solutions of the active ingredient by its rapid disappearance from the vehicle, and thereby maximizes the thermodynamic activity of the drug.

摘要

考虑到N,N - 二乙基间甲苯甲酰胺(避蚊胺)和1 - 十二烷基氮杂环庚烷 - 2 - 酮(氮酮)对硝苯地平(NP)热力学活性的影响,研究了它们对皮肤渗透性的影响。通过测量大鼠血浆中的药物浓度来确定NP的经皮吸收效率。对NP在促进剂中的悬浮液进行比较,以确保具有相等的热力学活性。与丙二醇(PG)相比,氮酮增加了NP的渗透,而避蚊胺产生了与PG相似的反应。与单独使用PG或癸二酸二乙酯(DES)相比,在PG或DES中添加少量避蚊胺可使NP的渗透大幅增加。本研究结果强烈表明避蚊胺和氮酮具有不同的作用方式。氮酮对皮肤产生了真正的影响,并使NP的渗透有显著改善。避蚊胺的作用很有趣,因为它仅在与其他载体组合时才有效。避蚊胺具有优异的增溶性能,易于穿透皮肤。因此,可以得出结论,避蚊胺仅作为助溶剂,通过其从载体中的快速消失产生活性成分的饱和或过饱和溶液,从而使药物的热力学活性最大化。

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