埃巴斯汀转移体的制备和评估

Guggila Niharika, Mekala Pallavi, Arumugam Yasodha
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引用次数: 0

摘要

本研究的重点是为体外研究配制和评估含有依巴斯汀的转运体制剂。研究人员采用冷冻法制备了转运体制剂,并对其体外特性和稳定性进行了评估。转运体制剂显示出最高的夹带效率和理想的粒径。扫描电镜分析表明,转运体制剂呈球形。与其他配方相比,含有脂质的转移体在 8 小时后的药物释放率较高。研究发现,F-2 配方在研究结束时的储存条件比较稳定。本研究表明,转运体凝胶制剂可持续、延长给药时间,提高生物利用度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and evaluation of Ebastine transferosomes
The present study was focused on formulating and evaluating Ebastine containing Transferosomes formulation for in vitro studies. Transferosomes formulations were prepared by using cold method and were evaluated for in vitro characteristics, stability studies. Transferosomes formulation displayed highest entrapment efficiency with desired particle size. SEM analyses showed that Transferosomes formulation was spherical in shape. Transferosomes containing lipid higher percentage of drug release after 8 h as compared to other formulations. F-2 formulation was found to be stable at the end of the study on storage condition. The present study suggested that Transferosomes gel formulations provide sustained and prolonged delivery of drug with enhance bioavailability.
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