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薄荷醇通过与药物形成低共熔物以及与皮肤脂质相互作用增强睾酮的皮肤渗透。

Testosterone skin permeation enhancement by menthol through formation of eutectic with drug and interaction with skin lipids.

作者信息

Kaplun-Frischoff Y, Touitou E

机构信息

Department of Pharmaceutics, School of Pharmacy, Hebrew University of Jerusalem, Israel.

出版信息

J Pharm Sci. 1997 Dec;86(12):1394-9. doi: 10.1021/js9701465.

Abstract

The aim of this investigation was to elucidate the mechanism of skin permeation enhancement of the lipophilic drug, testosterone, by menthol. Menthol was found to form eutectic mixtures with testosterone, cholesteryl oleate, and ceramides. DSC measurements showed that menthol drastically lowers the Tm of testosterone, from 153.7 to 39.9 degrees C. The decrease in Tm resulted in an increase in the solubility of testosterone in an aqueous ethanol vehicle by 2.8-fold, which caused a corresponding 2.8-fold increase in the flux of testosterone. A further increase in skin flux, to eight times the base line, could be attributed to the effect of menthol on the skin barrier properties. This assumption is supported by DSC results showing that menthol decreases the Tm of cholesteryl oleate and ceramides and modifies the thermogram profile of isolated stratum corneum. The results of this investigation indicate that menthol affects skin permeation by a dual mechanism: by forming a eutectic with the penetrating compound, thereby increasing its solubility, and by altering the barrier properties of the stratum corneum. Moreover, this study indicates that both types of interactions must be taken into consideration when using chemical enhancers and that decreasing the melting temperature of the permeant through formation of a eutectic could be one approach for increasing solubility and permeation rates.

摘要

本研究的目的是阐明薄荷醇增强亲脂性药物睾酮经皮渗透的机制。研究发现,薄荷醇能与睾酮、胆甾醇油酸酯和神经酰胺形成低共熔混合物。差示扫描量热法(DSC)测量结果表明,薄荷醇可使睾酮的熔点大幅降低,从153.7℃降至39.9℃。熔点的降低导致睾酮在乙醇水介质中的溶解度增加了2.8倍,相应地,睾酮的通量也增加了2.8倍。皮肤通量进一步增加至基线的8倍,这可能归因于薄荷醇对皮肤屏障特性的影响。DSC结果支持了这一假设,即薄荷醇降低了胆甾醇油酸酯和神经酰胺的熔点,并改变了离体角质层的热分析图谱。本研究结果表明,薄荷醇通过双重机制影响皮肤渗透:与渗透化合物形成低共熔物,从而增加其溶解度;改变角质层的屏障特性。此外,本研究表明,在使用化学渗透促进剂时,必须考虑这两种相互作用类型,并且通过形成低共熔物来降低渗透剂的熔点可能是提高溶解度和渗透速率的一种方法。

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