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首页> 外文期刊>Bulletin of Faculty of Pharmacy, Cairo University >Novel expandable gastro retentive system by unfolding mechanism of levetiracetam using simple lattice design – Formulation optimization and in vitro evaluation
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Novel expandable gastro retentive system by unfolding mechanism of levetiracetam using simple lattice design – Formulation optimization and in vitro evaluation

机译:通过简单的点阵设计通过左乙拉西坦的展开机理开发的新型可膨胀胃滞留系统–配方优化和体外评估

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摘要

The aim of the present study was to develop and characterize a novel expandable gastro-retentive dosage form (GRDF), based on unfolding mechanism. The dosage form consists of a drug loaded the polymeric patch, folded into a hard gelatin capsule. Gastro retention obtained from unfolding and swelling of the patch and its adhesion to the gastric mucosa. Therefore in this work, a gastro retentive patch of levetiracetam was developed using simple lattice design considering concentration of Hydroxy Propyl Methyl Cellulose, Carbopol 934P and Xanthan gum as independent variables. A response surface plot and multiple regression equations were used to evaluate the effect of independent variables on dependent variables such as mucoadhesive strength (g/cm 2 ) and t 90 (h). The prepared patches were evaluated for weight and thickness variation, mechanical properties, in vitro drug release and unfolding behavior. The absence of drug-polymer interaction and uniform drug dispersion in the polymeric patches was revealed by FT-IR, DSC, XRD and SEM. The results indicates, the novel GRDF based on unfolding mechanism can be alternative for other mucoadhesive dosage forms which will provide sustained release for 12 h.
机译:本研究的目的是基于展开机制,开发和表征一种新型的可扩展的胃滞留剂型(GRDF)。该剂型由载有聚合物贴剂的药物组成,折叠成硬明胶胶囊。胃贴片的展开和肿胀及其与胃粘膜的粘附,从而保留了胃。因此,在这项工作中,使用简单的点阵设计开发了左乙拉西坦的胃固性贴剂,将羟丙基甲基纤维素,Carbopol 934P和黄原胶的浓度作为独立变量。使用响应表面图和多个回归方程式来评估自变量对诸如粘膜粘附强度(g / cm 2)和t 90(h)等因变量的影响。对制备的贴剂的重量和厚度变化,机械性能,体外药物释放和展开行为进行评估。 FT-IR,DSC,XRD和SEM证实在聚合物贴片中没有药物-聚合物相互作用和均匀的药物分散。结果表明,基于展开机制的新型GRDF可以替代其他粘膜粘附剂型,提供12 h的持续释放。

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