罗望子多糖基质片的制备及评价

Ruchira Vasant Mahavarkar, S. Ahirrao, S. Kshirsagar, V. Rayate
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引用次数: 4

摘要

目的:采用天然聚合物修饰双氯芬酸钠在基质片中的释放速度。从豆科罗望子果实中天然提取的罗望子籽多糖等基质形成剂在片剂中表现出缓释特性。方法:采用湿法造粒法制备双氯芬酸钠缓释片。结果:OF1和OF2均为优化批次。对优化制剂(Voveran- SR)和上市制剂(Voveran- SR)进行体外溶出度研究。结果表明,10 h时的优化批数分别为90.27%和90.18%。结论:罗望子多糖可作为缓释药物的剂型。用不同浓度的罗望子多糖(TSP)配制片剂,释药时间可达10小时以上。OF1和OF2两种制剂与市售制剂具有相当的释放度。从目前的工作可以得出结论,在研究开始时设定的目标得到了实现。
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 tamarind seed polysaccharide matrix tablet
Objective: The objective of using natural polymer was to modify the release rate of Diclofenac sodium from matrix tablet. The matrix forming agent like Tamarind seed Polysaccharide show sustained release property in tablet which is obtained naturally from fruit of Tamarindus indica L. belonging to Family Leguminosae. Methods: The sustained release matrix tablet of Diclofenac sodium were prepared by wet granulation technique using varying concentration of hydrophilic polymer i.e. TSP. Results: OF1 and OF2 both are optimized batch. The in vitro dissolution study was carried out for optimized as well as marketed formulation (Voveran- SR). Both the optimized batchesat 10 h were found to be 90.27% and 90.18%, respectively. Conclusions: Tamarind seed polysaccharide can be employed in dosage form to sustain the drug release. Tablet formulated with various concentrations of Tamarind seed polysaccharide (TSP) gives release up to 10 h and more. OF1 and OF2 both formulations give comparable release with marketed formulation. From the present work it can be conclude that, the objectives which were set at the beginning of the study got fulfilled.
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