Suppr超能文献

甘油酯基质药物释放机制的评估。

An evaluation of the mechanisms of drug release from glyceride bases.

作者信息

Sutananta W, Craig D Q, Newton J M

机构信息

Centre for Materials Science, School of Pharmacy, University of London, UK.

出版信息

J Pharm Pharmacol. 1995 Mar;47(3):182-7. doi: 10.1111/j.2042-7158.1995.tb05775.x.

Abstract

A series of dispersions containing theophylline in Gelucires 43/01, 54/02, 50/02, 50/13 and 55/18 was prepared and the physical structures studied using differential scanning calorimetry. The dissolution, erosion and swelling profiles of the drug dispersions were assessed. Gelucire 43/01 and 54/02 systems were found to release the drug by a simple diffusion mechanism, with no evidence for erosion or swelling being noted. Gelucire 55/18, however, showed a more complex mechanism involving both diffusion and erosion. On increasing the drug load within the matrices, the predominance of the erosion mechanism increased. Drug release from Gelucire 50/13 matrices took place principally by erosion, although the process was dominated by swelling and subsequent disintegration of the matrix, rather than simple dissolution of the base as was found for Gelucire 55/18. Gelucire 50/02 matrices also exhibited swelling, although drug release occurred predominantly via diffusion. The study, therefore, demonstrates that Gelucires may release incorporated drugs by a number of mechanisms depending on the chemical composition of the base.

摘要

制备了一系列含有氨茶碱的Gelucire 43/01、54/02、50/02、50/13和55/18的分散体,并使用差示扫描量热法研究其物理结构。评估了药物分散体的溶解、侵蚀和溶胀曲线。发现Gelucire 43/01和54/02体系通过简单扩散机制释放药物,未观察到侵蚀或溶胀迹象。然而,Gelucire 55/18显示出一种更复杂的机制,涉及扩散和侵蚀。随着基质中药物载量的增加,侵蚀机制的主导作用增强。Gelucire 50/13基质中的药物释放主要通过侵蚀发生,尽管该过程以基质的溶胀和随后的崩解为主导,而不是像Gelucire 55/18那样以基质的简单溶解为主导。Gelucire 50/02基质也表现出溶胀,尽管药物释放主要通过扩散发生。因此,该研究表明,根据基质的化学成分,Gelucire可能通过多种机制释放包封的药物。

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