Solubility And Dissolution Enhancement of Budesonide by Solid Dispersion Using Rotary Evaporation Technique

Ajit B Patil, Aishwarya Jadhav, Afaque Ansari, Rushabh Jain, Yogesh Darade, Shraddha Birajdar
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Abstract

The Purpose of the work was to enhance the solubility and dissolution of Budesonide API Powder which was under BCS Class 2 system. Solid dispersion of Budesonide were prepared by using different polymers like Poly vinyl pyrrolidone (PVP K30), polyethylene glycol 6000 (PEG6000) by using Solvent Evaporation Method by using Rotary Evaporator, in the 1:1:1, 1:1:2, 1:1:3, 1:2:1, ratios of drug and carrier. The In-vitro release profile of all solid dispersions (F1 to F9) were comparatively evaluated and also studied against pure Budesonide. The evaluation test were carried out like drug content, solubility, drug release studies. The drug and polymer interaction was studied by using Fourier Transport Infra-Red and Differential Scanning Calorimetry, Powder X Ray Diffraction studies were also carried out to find out the Crystalinity of Solid Dispersion, SEM was carried out for study of surface morphology.
利用旋转蒸发技术通过固体分散提高布地奈德的溶解度和溶解度
这项研究的目的是提高布地奈德原料药粉末的溶解度和溶出度,该原料药粉末属于 BCS 2 级系统。利用旋转蒸发器,采用溶剂蒸发法,按照 1:1:1、1:1:2、1:1:3、1:2:1 的药物和载体比例,使用聚乙烯吡咯烷酮(PVP K30)、聚乙二醇 6000(PEG6000)等不同聚合物制备布地奈德固体分散体。对所有固体分散体(F1 至 F9)的体外释放曲线进行了比较评估,并与纯布地奈德进行了对比研究。评估测试包括药物含量、溶解度和药物释放研究。使用傅立叶红外传输和差示扫描量热法研究了药物与聚合物的相互作用,还进行了粉末 X 射线衍射研究,以确定固体分散体的结晶度,并使用扫描电镜研究了表面形态。
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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