含氟比洛芬成膜凝胶的研制

S. N. Albhar
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引用次数: 1

摘要

本研究以卡波波尔934为胶凝剂,研制氟比洛芬成膜凝胶配方,用于局部给药,以避免肝初过代谢,提高乳剂稳定性,减少给药方案,延长停留时间,用于治疗类风湿关节炎。成膜凝胶已成为最有趣的局部给药系统之一,因为它具有双重释放控制,即膜和凝胶。对制备的凝胶进行了理化性质评价,如颜色、均匀性、稠度、铺展性、pH值、流变学行为、药物含量、药物释放和稳定性。所制备的成膜凝胶在颜色、均匀性、稠度、涂抹性和pH值等方面均表现出满意的理化性能。与其他制剂相比,优化制剂的药物释放度更高。F2的药物含量最高,即;98.66%。所有凝胶的药物释放均遵循扩散控制机制。稳定性研究表明,所有制备的凝胶在储存3个月后,其物理外观、流变性能、涂抹性、药物含量均保持不变。
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FORMULATION AND DEVELOPMENT OF FLURBIPROFEN CONTAINING FILM FORMING GEL
The purpose of present research work was to develop a Film Forming gel formulation of flurbiprofen using carbopol 934 as a gelling agent for topical delivery with the aim to avoid hepatic first pass metabolism, improve stability of emulsion, reduce dosage regimen and enhance residence time in the treatment of Rheumatoid arthritis. Film Forming gels have emerged as one of the most interesting topical drug delivery systems as it has dual release control i.e. Film and gel. The developed gels were evaluated for their physicochemical properties like color, homogeneity, consistency, spreadability, pH value, rheological behaviour, drug content, drug release and stability. All the prepared film forming gels showed satisfactory physicochemical properties like color, homogeneity, consistency, spreadability, and pH value. The drug release was found to be higher for optimized formulation as compared to the other prepared formulations. The highest drug content was observed with F2, i.e; 98.66%. The drug releases from all the gels were found to follow diffusion-controlled mechanism. Stability studies indicated that the physical appearance, rheological properties, spreadability, drug content in all the prepared gels remained unchanged upon storage for 3 months.
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