天然聚合物基多潘立酮漂浮基质片

Sheeba Fr, Amar Sahani, Yogesh Db
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引用次数: 0

摘要

目的:利用天然聚合物制备马来酸多潘立酮漂浮基质片。材料与方法:将马来酸多潘立酮配制为漂浮基质片,增加其胃停留时间。采用黄原胶、黄原胶、海藻酸钠等天然聚合物和碳酸氢钠、柠檬酸、HPMC等天然聚合物增加了浮时间,减少了浮滞时间。对压片的脆度、硬度、重量均匀性、含量均匀性、溶胀指数、弹性时间、体外释药等参数进行评价。结果:评价参数符合药典规定。最成功的配方是F2,以黄原胶为聚合物。药物释放时间延长至10 h,与理论释放曲线接近。体外溶出度数据的数学模型表明,该药物的释放动力学符合零级模型,R2值为0.99。结论:制备的马来酸多潘立酮缓释片治疗效果优于常规缓释片,疗效更高,患者依从性更好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural Polymer Based Floating Matrix Tablets of Domperidone
Aim: This study is aimed to prepare floating matrix Domperidone Maleate tablets by using natural polymers. Materials and Methods: Domperidone maleate was formulated as floating matrix tablets to increase the gastric residence time. Natural polymers like xanthan gum, tragacanth, sodium alginate along with sodium bicarbonate, citric acid and HPMC were used to increase the buoyancy time and decrease the floating lag time. The compressed tablets were evaluated for various parameters like friability, hardness, uniformity of weight, uniformity of drug content, swelling index, bouncy time and in-vitro drug release. Results: The evaluated parameters were in compliance with the pharmacopoeial limits. The most successful formulation was F2, containing xanthan gum as polymer. The drug release was extended up to 10 h which was close to that of theoretical release profile. Mathematical modelling of in-vitro dissolution data indicated the best-fit release kinetics was achieved with Zero order model with R2 values of 0.99. Conclusion: The prepared sustained-release floating tablets of domperidone maleate could perform therapeutically better than that of conventional sustained release tablets with improved efficacy and better patient compliance.
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