Suppr超能文献

甲基黄嘌呤经人体组织的体外透皮和颊部给药

Transdermal and buccal delivery of methylxanthines through human tissue in vitro.

作者信息

Thakur Rashmi A, Michniak Bozena B, Meidan Victor M

机构信息

Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.

出版信息

Drug Dev Ind Pharm. 2007 May;33(5):513-21. doi: 10.1080/03639040600901994.

Abstract

We examined the in vitro permeation of central nervous stimulants - caffeine, theophylline, and theobromine across human skin with the aid of six chemical enhancers. It was found that oleic acid was the most potent enhancer for all three methylxanthines. Further optimization studies with different solvents showed that caffeine transport could be enhanced to give flux values up to 585 microg/cm2.hr-1. Theobromine and theophylline delivery rates proved insufficient. An additional study involving a buccal tissue equivalent showed that this membrane was more permeable than skin for all model actives tested and would offer an alternate way of delivery.

摘要

我们借助六种化学增强剂研究了中枢神经兴奋剂——咖啡因、茶碱和可可碱在人皮肤上的体外渗透情况。结果发现,油酸是这三种甲基黄嘌呤最有效的增强剂。使用不同溶剂进行的进一步优化研究表明,咖啡因的转运可得到增强,通量值可达585微克/平方厘米·小时-1。可可碱和茶碱的释放速率则不足。另一项涉及口腔组织替代物的研究表明,对于所有测试的模型活性物质,该膜比皮肤更具渗透性,可提供另一种给药途径。

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