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Drug release behavior of polymeric matrix filled in capsule

机译:填充在胶囊中的聚合物基质的药物释放行为

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A single unit sustainable drug release system was developed using hydroxypropyl methylcellulose (HPMC)-based matrices filled in capsule as the drug delivery device. Release behavior of propranolol HCl from these capsules was investigated and least square fitting was performed for the dissolution data with the different mathematical expressions. Effect of diluent, polymer, pH and hydrodynamic force on the drug release from the developed systems was investigated. The utilization of HPMC as a matrix former extended the drug release longer than 8h. HPMC viscosity grades affected the drug release, that is, increasing the amount of fillers such as lactose and dibasic calcium phosphate enhanced the drug release rate of HPMC matrices. The hydrodynamic force, type and amount of incorporated polymer apparently influenced the drug release. The physiochemical properties of polymers and interaction between HPMC and other polymers were important factors for prolongation of the drug release. The release mechanism from HPMC-based matrices in capsules was the non-Fickian transport in which the sustainable drug release of HPMC capsules could be achieved by the addition of polymeric matrix.
机译:使用填充在胶囊中的基于羟丙基甲基纤维素(HPMC)的基质作为药物输送装置,开发了一种单位可持续药物释放系统。研究了盐酸普萘洛尔从这些胶囊中的释放行为,并用不同的数学表达式对溶出度数据进行了最小二乘拟合。研究了稀释剂,聚合物,pH和流体动力对已开发系统中药物释放的影响。 HPMC作为基质形成剂的使用将药物释放延长了8小时以上。 HPMC粘度等级会影响药物释放,也就是说,增加填充剂(如乳糖和磷酸氢二钙)的数量会增加HPMC基质的药物释放速率。流体动力,聚合物的类型和数量显然影响药物释放。聚合物的理化性质以及HPMC与其他聚合物之间的相互作用是延长药物释放的重要因素。胶囊中基于HPMC的基质的释放机理是非菲克转运,通过添加聚合基质可以实现HPMC胶囊的可持续药物释放。

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