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使用天然油制备难溶性药物自乳化给药系统及其性质研究

Development and characterization of self emulsifying drug delivery system of a poorly water soluble drug using natural oil.

作者信息

Sharma Shivani, Bajaj Himani, Bhardwaj Piyush, Sharma Anshul Dutt, Singh Ranjeet

机构信息

Adarsh Vijendra Institute of Pharmaceutical Sciences, Gangoh Saharanpur (U.P), India.

出版信息

Acta Pol Pharm. 2012 Jul-Aug;69(4):713-7.

Abstract

Objective of present study involves preparation and evaluation of self emulsifying drug delivery system (SEDDS) of ibuprofen using peanut oil. SEDDS were composed of varying concentrations of peanut oil (solvent), tween 80 (surfactant) and span 20 (co-surfactant). Influence of concentration of surfactant/co-surfactant and globule size on dissolution rate was investigated. Dissolution rate was studied in phosphate buffer pH 6.8 using dissolution apparatus II. The dissolution rate of self emulsifying capsule was found to be significantly faster than that from conventional tablet. The optimized SEDDS released approximately above 85% of ibuprofen within 30 min, while conventional ibuprofen tablet could released only 36% in 30 min. Therefore, these SEDDS could be a better alternative to conventional drug delivery system of ibuprofen.

摘要

本研究的目的是制备并评估使用花生油的布洛芬自乳化药物递送系统(SEDDS)。SEDDS由不同浓度的花生油(溶剂)、吐温80(表面活性剂)和司盘20(助表面活性剂)组成。研究了表面活性剂/助表面活性剂浓度和球粒大小对溶解速率的影响。使用溶出度仪II在pH 6.8的磷酸盐缓冲液中研究溶解速率。发现自乳化胶囊的溶解速率明显快于传统片剂。优化后的SEDDS在30分钟内释放了约85%以上的布洛芬,而传统布洛芬片剂在30分钟内仅释放36%。因此,这些SEDDS可能是布洛芬传统药物递送系统的更好替代品。

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