Development and characterization of Decitabine Niosomes

Buruju Vennela, Arumugam Siva Kumar, Kassa Jyothi, Arumugam Yasodha
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引用次数: 0

Abstract

The present study was focused on formulating and evaluating Decitabine containing niosomes formulation for In Vitro studies. Niosomal formulations were prepared by using different ratio of surfactant (Tween 80 and Tween 20) and cholesterol by thin film hydration method and were evaluated for In Vitro characteristics, stability studies. Span 20 containing niosomal formulation displayed highest entrapment efficiency with desired particle size. SEM analyses showed that niosomal formulation was spherical in shape. Niosomes containing Tween 20 displayed higher percentage of drug release after 8 h as compared to other formulations. F-7 formulation was found to be stable at the end of the study on storage condition. The present study suggested that niosomal formulations provide sustained and prolonged delivery of drug with enhance bioavailability.
地西他滨新药的开发和特征描述
本研究的重点是为体外研究配制和评估含有地西他滨的niosomes配方。使用不同比例的表面活性剂(吐温 80 和吐温 20)和胆固醇,通过薄膜水合法制备了niosomal 配方,并对其进行了体外特性和稳定性研究。含有吐温 20 的niosomal 配方显示出最高的吸附效率和理想的粒度。SEM 分析表明,niosomal 配方呈球形。与其他制剂相比,含吐温 20 的尼索莫制剂在 8 小时后的药物释放率较高。在研究结束时,发现 F-7 配方在储存条件下是稳定的。本研究表明,含糖体制剂可持续和延长给药时间,提高生物利用率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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