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Effect of formulation variables on preparation and evaluation of gelled self-emulsifying drug delivery system (SEDDS) of ketoprofen

机译:配方变量对酮洛芬凝胶自乳化药物递送系统(SEDDS)的制备和评估的影响

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摘要

The purpose of this study was to formulate a gelled self-emulsifying drug delivery system (SEDDS) containing ketoprofen as an intermediate in the development of sustained release solid dosage form. Captex 200 (an oil), Tween 80 (a surfactant), and Capmul MCM (a cosurfactant) were used to formulate SEDDS. Silicon dioxide was used as a gelling agent, which may aid in solidification and retardation of drug release. Effect of concentrations of cosurfactant and gelling agent on emulsification process and in vitro drug diffusion was studied using 32 factorial design. Multiple regression analysis data and response surfaces obtained showed that liquid crystal phase viscosity increased significantly with increasing amount of silicon dioxide, which in turn caused an increase in average droplet size of resultant emulsion and slower drug diffusion. Drug release from the formulation increased with increasing amount of cosurfactant.
机译:这项研究的目的是配制一种以酮洛芬为中间体的凝胶状自乳化药物递送系统(SEDDS),用于开发缓释固体剂型。使用Captex 200(油),Tween 80(表面活性剂)和Capmul MCM(助表面活性剂)配制SEDDS。二氧化硅用作胶凝剂,可以帮助固化和延缓药物释放。使用32因子设计研究了助表面活性剂和胶凝剂浓度对乳化过程和体外药物扩散的影响。多元回归分析数据和获得的响应面表明,液晶相粘度随着二氧化硅含量的增加而显着增加,这反过来导致所得乳液的平均液滴尺寸增加,药物扩散较慢。制剂中药物的释放随着辅助表面活性剂含量的增加而增加。

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