首页> 外文期刊>Bulletin of pharmaceutical sciences >BUCCOADHESIVE TABLETS FOR DELIVERY OF VERAPAMIL HC1: DESIGN, IN- VITRO ANALYSIS AND IN- VIVO EVALUATION
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BUCCOADHESIVE TABLETS FOR DELIVERY OF VERAPAMIL HC1: DESIGN, IN- VITRO ANALYSIS AND IN- VIVO EVALUATION

机译:维拉帕米HC1的胶粘剂片剂:设计,体外分析和体内评估

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Buccoadhesive controlled release verapamil HCl tablets have been prepared using mucoadhesive polymers namely; sodium alginate (Na Alg), xanthan gum (XG) and gum tragacanth (GT) either alone or in combination in different ratios 2:8, 8:2, 4:6 and 6:4. The prepared tablets were evaluated for their weight variation, thickness, hardness, friability and dissolution, content uniformity, swelling index, in-vitro adhesion, in-vitro drug release and in-vivo hypertension study. Tablets containing XG showed the highest swelling index and bioadhesive force. The maximum cumulative % released (100%) was observed in F7, F10 and Fll due to high percent ofNa alg. The kinetics studies show that the release follows zero order kinetics except Fl that it obeyes a diffusion model. The buccoadhesive verapamil HCl tablet had suggested being promising for the transmucosal delivery of verapamil HCl and allowing a controlled drug delivery for 6 hrs.
机译:已经使用粘膜粘附性聚合物制备了颊粘膜控释维拉帕米HCl片剂。海藻酸钠(Na Alg),黄原胶(XG)和黄aga胶(GT)可以单独使用或以2:8、8:2、4:6和6:4的不同比例组合使用。评价所制备的片剂的重量变化,厚度,硬度,易碎性和溶解性,含量均匀性,溶胀指数,体外粘附,体外药物释放和体内高血压研究。含XG的片剂显示出最高的溶胀指数和生物粘附力。由于较高的Na alg百分比,在F7,F10和Fll中观察到最大累积释放百分比(100%)。动力学研究表明,释放遵循零级动力学,除了F1服从扩散模型。含颊粘膜的维拉帕米HCl片剂有望通过粘膜输送维拉帕米HCl,并允许6个小时的受控药物递送。

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