Suppr超能文献

采用扩散池的经皮药物体外传输。

Transdermal drug delivery in vitro using diffusion cells.

机构信息

Department of Toxicology, Faculty of Military Health Sciences, University of Defence, Trebesska 1575, 50001 Hradec Kralove, Czech Republic.

出版信息

Curr Med Chem. 2012;19(27):4671-7. doi: 10.2174/092986712803306358.

Abstract

The assessment of percutaneous absorption of molecules is a very important step in the evaluation of any dermal or transdermal drug delivery system. In order to perform percutaneous drug absorption studies, it is essential that the methods are standardized and that the integrity of the skin is monitored and maintained to ensure that the data obtained are valid and relevant. Reproducible data on percutaneous absorption in humans are as well required to predict the systemic risk from dermal exposure to chemicals, such as hazardous substances at the workplace, agrochemicals and cosmetic ingredients. In vitro and animal models provide important tools for screening a series of drug formulations, evaluation of skin permeation enhancing properties and mechanism of action of the carrier systems and estimation of rank of skin transport for a series of drug molecules. In this review, we have summarized in vitro testing of skin absorption using static Franz-type diffusion cells.

摘要

评估分子的经皮吸收是评价任何皮肤或透皮药物传递系统的非常重要的步骤。为了进行经皮药物吸收研究,必须使方法标准化,并监测和维持皮肤的完整性,以确保获得的数据有效且相关。还需要在人类中进行可重复的经皮吸收数据,以预测化学物质(如工作场所的危险物质、农药和化妆品成分)经皮暴露的全身风险。体外和动物模型为筛选一系列药物制剂、评估皮肤渗透增强特性和载体系统的作用机制以及估计一系列药物分子的皮肤转运等级提供了重要工具。在这篇综述中,我们总结了使用静态 Franz 型扩散池进行皮肤吸收的体外测试。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验