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Studies on formulation and in vitro evaluation of floating matrix tablets of domperidone

机译:多潘立酮漂浮基质片剂的制备及体外评价研究

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摘要

Floating matrix tablets of domperidone were developed to prolong gastric residence time and thereby increased drug bioavailability. Domperidone was chosen as a model drug because it is poorly absorbed from the lower gastrointestinal tract. The tablets were prepared by wet granulation technique, using polymers such as hydroxypropylmethylcellulose K4M, carbopol 934P, and sodium alginate, either alone or in combination, and other standard excipients. Tablets were evaluated for physical characteristics viz. hardness, % friability, floating capacity, weight variation and content uniformity. Further, tablets were evaluated for in vitro release characteristics for 24 h. In vitro release mechanism was evaluated by linear regression analysis. Floating matrix tablets based on combination of three polymers namely; hydroxypropylmethylcellulose K4M, carbopol 934P and sodium alginate exhibited desired floating and prolonged drug release for 24 h. Carbopol loading showed negative effect on floating properties but were found helpful to control the release rate of drug.
机译:开发了多潘立酮漂浮基质片剂以延长胃停留时间,从而增加药物的生物利用度。选择多潘立酮作为模型药物,因为它在下消化道吸收差。通过湿法制粒技术,使用单独或组合的聚合物,例如羟丙基甲基纤维素K4M,carbopol 934P和海藻酸钠,以及其他标准赋形剂,制备片剂。评价片剂的物理特性,即。硬度,脆碎度,浮动能力,重量变化和含量均匀性。此外,评估片剂24小时的体外释放特性。通过线性回归分析评估了体外释放机理。基于三种聚合物组合的浮体片剂:羟丙基甲基纤维素K4M,卡波姆934P和海藻酸钠表现出所需的漂浮性和24小时的药物释放时间。卡波姆负荷对漂浮特性显示出负面影响,但被发现有助于控制药物的释放速率。

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