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Design and Evaluation of Extended Release Tablets of Pramipexole dihydrochloride monohydrate

机译:盐酸普拉克索一水合物缓释片的设计与评价

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The objective of the present study was to develop and characterize extended release tablets of Pramipexole dihydrochloride monohydrate to be taken once daily. The combination of different polymers like hydroxypropyl methyl cellulose (HPMC K 100M) and Eudragit L 100 in varying concentrations were studied to get the desired extended release profile over a period of 24 h. The granules were evaluated for angle of repose, bulk density, compressibility index, and drug content and found to be satisfactory. Hydroxypropylmethylcellulose (HPMC K100M) at 50% level in combination with methacrylic acid copolymer (Eudragit L100) at 2.0% level producedextended release Pramipexole dihydrochloride monohydrate matrix tablets. The drug release of optimized formulation (F7) was extended up to 24 h in vitro study. The drug release pattern from the optimized matrix formulation (F7) was diffusion controlled. The innovator product Mirapex (0.375 mg) drug release profiles are shown to be followed first order release kinetics. The results suggested that combination of hydrophilic and hydrophobic polymers used in the preparation of extended release Pramipexole dihydrochloride monohydrate tablets, is a suitable method and it can perform therapeutically better.
机译:本研究的目的是开发和表征普拉克索二盐酸盐一水合物的缓释片,每天服用一次。研究了不同浓度的不同聚合物(如羟丙基甲基纤维素(HPMC K 100M)和Eudragit L 100)的组合,可在24小时内获得所需的延长释放曲线。评价颗粒的休止角,堆积密度,可压缩性指数和药物含量,发现令人满意。以50%的羟丙基甲基纤维素(HPMC K100M)与以2.0%的甲基丙烯酸共聚物(Eudragit L100)组合制成缓释普拉克索二盐酸盐一水合物基质片剂。优化的制剂(F7)的药物释放延长至体外研究24小时。优化基质制剂(F7)的药物释放模式受到扩散控制。已显示创新产品Mirapex(0.375 mg)的药物释放曲线遵循一级释放动力学。结果表明,用于制备缓释普拉克索二盐酸盐一水合物片剂的亲水性和疏水性聚合物的组合是一种合适的方法,并且可以实现更好的治疗效果。

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