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布洛芬及布洛芬蜡质微球缓释制剂混悬液的化学、溶出稳定性及微观评价

Chemical, dissolution stability and microscopic evaluation of suspensions of ibuprofen and sustained release ibuprofen-wax microspheres.

作者信息

Adeyeye C M, Price J C

机构信息

Graduate School of Pharmaceutical Sciences, Duquesne University, Pittsburgh, Pennsylvania, USA.

出版信息

J Microencapsul. 1997 May-Jun;14(3):357-77. doi: 10.3109/02652049709051139.

Abstract

Chemical stability studies of suspensions of ibuprofen powder and ibuprofen-wax microspheres were performed using an accelerated stability protocol with a modified high performance liquid chromatography (HPLC) procedure. The variables considered were pH, suspending agents and temperature. The study showed little or no chemical degradation in the different suspending agents after storage for three months. Dissolution stability was examined in suspensions of ibuprofen microspheres made from an optimized formulation with 17% drug loading. The storage temperature were 23, 37 and 45 degrees C. Other variables for the dissolution stability studies were suspending agents, wax types, suspending medium pH and microsphere size. Suspensions of ceresine wax microspheres stored at 37 degrees C showed faster drug release than room temperature storage, but suspensions stored at 45 degrees C showed an opposite effect. Microspheres suspended in syrup and stored at 37 degrees C had faster dissolution rates than microspheres suspended in methylcellulose at the same temperature, possibly as a result of an interaction between the syrup and the microsphere constituents. Suspensions of microcrystalline wax microspheres had better dissolution stability than microspheres made from ceresine wax. Higher suspending medium pH resulted in faster release of drug from the suspended microspheres, but particle size did not significantly affect the dissolution stability.

摘要

采用改良高效液相色谱(HPLC)法的加速稳定性试验方案,对布洛芬粉末混悬液和布洛芬蜡微球进行了化学稳定性研究。考察的变量包括pH值、助悬剂和温度。研究表明,在不同助悬剂中储存三个月后,化学降解很少或没有发生。对载药量为17%的优化配方制备的布洛芬微球混悬液进行了溶出稳定性研究。储存温度为23、37和45摄氏度。溶出稳定性研究的其他变量包括助悬剂、蜡的类型、混悬介质pH值和微球大小。在37摄氏度储存的微晶蜡微球混悬液比在室温储存时药物释放更快,但在45摄氏度储存的混悬液则呈现相反的效果。在37摄氏度储存的糖浆中混悬的微球比在相同温度下甲基纤维素中混悬的微球溶出速率更快,这可能是由于糖浆与微球成分之间相互作用的结果。微晶蜡微球混悬液比微晶蜡制成的微球具有更好的溶出稳定性。较高的混悬介质pH值导致混悬微球中药物释放更快,但粒径对溶出稳定性没有显著影响。

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