结晶度
溶解
吸附
多孔性
毒品携带者
溶剂
材料科学
药品
齐拉西酮
化学工程
色谱法
化学
核化学
药理学
有机化学
医学
复合材料
氯氮平
精神分裂症(面向对象编程)
工程类
精神科
作者
Ashok Mahajan,Ashish Yadav,Priyal Patel,Shailesh Koradia,Falgun Mehta,Kautuk Shah
出处
期刊:Research journal of pharmacy and technology
[Diva Enterprises Private Limited]
日期:2021-04-29
卷期号:: 1899-1904
被引量:1
标识
DOI:10.52711/0974-360x.2021.00335
摘要
The objective of present investigation was comparison of porous carriers to increase the dissolution properties of BCS class II drug Ziprasidone. Solvent evaporation method was used for the adsorption of ziprasidone on various porous carriers. Three different porous carriers namely Florite, Neusilin US2, Sylysia 350 were used in the study. Prepared microparticles were characterised for invitro drug release, SEM, XRD and DSC. The optimized formulation containing ziprasidone: florite microparticles had high drug release (94.88% in 45 min) than plain ziprasidone tablets (21.13% in 45 min) which is due to increase in surface area and decrease in crystallinity of drug after adsorption onto porous carrier.
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