Suppr超能文献

Stability of liposomal formulations in physiological conditions for oral drug delivery.

作者信息

Taira M C, Chiaramoni N S, Pecuch K M, Alonso-Romanowski S

机构信息

Laboratory of Biomembranes, Departamento de Ciencia y Tecnología, Universidad Nacional de Quilmes, Bernal, Argentina.

出版信息

Drug Deliv. 2004 Mar-Apr;11(2):123-8. doi: 10.1080/10717540490280769.

Abstract

The stability of liposomal formulations is a key issue in drug delivery. Liposomes made of egg phosphatidylcholine (EPC), cholesterol (Chol), sphingomyelin (SM), and gangliosides (GM1 and GM type III) were incubated in different media to determine their stability. Mixtures containing GM1 or GM type III were found to be the most stable, and both showed similar stability trends in plasma at 37 degrees C. EPC/Chol was the most susceptible to lysis in plasma. In acid media (pH 2), the highest stability corresponded to EPC/Chol, whereas in bile and pancreatin, liposomes with GM1 and GM type III were more stable than those containing SM. This study suggests that among the formulations used as oral drug carriers, those containing GM1 and GM type III have higher possibilities of surviving through the gastrointestinal tract.

摘要

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验