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Design and in vitro testing of a floatable gastroretentive tablet of metformin hydrochloride.

机译:盐酸二甲双胍可漂浮性胃滞留片剂的设计和体外测试。

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Metformin hydrochloride, which is better absorbed in the upper intestine, was formulated as a floating (buoyant) matrix tablet using a gas generating agent (sodium bicarbonate) and a gel forming hydrophilic polymer (hydroxypropyl methylcellulose). The formulation was optimized on the basis of floating ability and in vitro drug release. The resulting formulation produced robust tablets with optimum hardness, consistent weight uniformity and low tablet friability. All tablets but one exhibited satisfactory (gradual and near complete) drug release and buoyancy. In vitro drug release tests of these tablets indicated controlled sustained release of metformin hydrochloride and 96-99% released at the end of 8 h. Two formulations of fabricated tablets containing metformin hydrochloride (500 mg), sodium bicarbonate (75 mg), hydroxypropyl methylcellulose-K 4M (170-180 mg), citric acid (between 15 and 20 mg) and polyvinyl pyrrolidone K90 (32-40 mg) with hardness between 6.8 to 7.5 kg/cm2 showed a floating time ofmore than 8 h and promising drug release results. The release followed the Higuchi kinetic model, indicating diffusion dominated drug release.
机译:使用产气剂(碳酸氢钠)和形成凝胶的亲水性聚合物(羟丙基甲基纤维素),将在上层小肠中更好吸收的盐酸二甲双胍制成漂浮(浮力)基质片剂。根据漂浮能力和体外药物释放对制剂进行了优化。所得制剂产生具有最佳硬度,一致的重量均匀性和低片剂脆性的坚固片剂。除一种片剂外,所有片剂均显示出令人满意的(逐渐的和接近完全的)药物释放和浮力。这些片剂的体外药物释放试验表明,盐酸二甲双胍的缓释具有控制性,在8小时结束时释放了96-99%。两种预制片剂的配方,分别含有盐酸二甲双胍(500 mg),碳酸氢钠(75 mg),羟丙基甲基纤维素-K 4M(170-180 mg),柠檬酸(15至20 mg)和聚乙烯吡咯烷酮K90(32-40 mg) )硬度在6.8至7.5 kg / cm2之间的材料显示出超过8小时的漂浮时间,并有望释放药物。释放遵循Higuchi动力学模型,表明扩散主导药物释放。

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