采用32因子设计制备胃内保留型奥氮平微球。

Deshmukh Mt, Mohite Sk
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引用次数: 0

摘要

以海藻酸钠和卡波醇974p为聚合物,氯化钙为交联剂,采用外肌力凝胶法制备奥氮平微球。在这个配方中,海藻酸钠和卡泊泊974p作为聚合物的组合,有助于延缓药物的释放,提高药物的生物利用度。所制备的奥氮平微球在药物含量、药物包封效率、P - XRD、差示扫描比色、FTIR、SEM、体外释药和体内释药等方面进行了表征。利用USP溶出仪研究了奥氮平微球在900 ml 0.1 N盐酸中的体外释放规律。优化批F7的释药率大于80%,这是由于使用了卡波醇聚合物,有助于延缓药物在目标部位的释放。与纯奥氮平相比,优化后的配方具有更好的抗抑郁作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation, optimization and characterization of gastro retentive olanzepine microsphere using 32 factorial design.
Olanzepine microsphere prepared by external Inotropic gelation technique by using sodium alginate and carbopol 974 P as a polymer and calcium chloride as a cross linking agent. In this formulation combination of sodium alginate and carbopol 974 P used as a polymer that helps to retard the releasing the drug and increases bioavaibility of drug. The Olanzepine microsphere has other characterization is in the term ofdrug content, drug entrapment efficiency, P XRD, Differential Scanning Colorimetry, FTIR , SEM, in vitro drug release and in vivo drug release. The in vitro release pattern of Olanzepine microsphere studied in 900 ml of 0.1 N Hydrochloric acids, using USP dissolution apparatus I. The optimized batch F7 shows greater than 80 % of drug release that is due to using carbopol polymer that helps to retarded the drug release at targeted site over the other formulation. Optimized formulation shows better antidepressant action as compare to pure Olanzepine drug.
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