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首页> 外文期刊>Carbohydrate Polymers: Scientific and Technological Aspects of Industrially Important Polysaccharides >Ca~(2+) ion cross-linked interpenetrating network matrix tablets of polyacrylamide-grafted-sodium alginate and sodium alginate for sustained release of diltiazem hydrochloride
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Ca~(2+) ion cross-linked interpenetrating network matrix tablets of polyacrylamide-grafted-sodium alginate and sodium alginate for sustained release of diltiazem hydrochloride

机译:Ca〜(2+)离子交联互穿网络基质片的聚丙烯酰胺接枝海藻酸钠和海藻酸钠用于盐酸地尔硫卓的缓释

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摘要

Interpenetrating network (IPN) matrix tablets of diltiazem-HCl (DTZ) was prepared by wet granulation method using polyacrylamide-grafted-sodium alginate (PAam-g-SAL) co-polymer and sodium alginate (SAL) for sustained release of the drug. Formulation of IPN structure was examined using FTIR spectroscopy, and compatibility of the drug with the polymers was evaluated through FTIR, DSC, and XRD analyses. The effect of co-polymer/SAL ratios, drug load, and total polymer/calcium gluconate (CG) ratios on drug release in acidic and phosphate buffer solutions was investigated. The release of drug was controlled by the relative magnitude of swelling capacity of IPN matrix and viscosity of the gel formed following dissolution of the polymers. The swelling capacity of the matrix was governed by the formation of calcium alginate gel structure and the rigidity imparted by the co-polymer. The results indicated that IPN matrix tablets of PAam-g-SAL and SAL could be used for sustained release of DTZ.
机译:采用聚丙烯酰胺接枝海藻酸钠(PAam-g-SAL)共聚物和海藻酸钠(SAL)湿法制粒,制备了地尔硫卓-HCl(DTZ)互穿网络(IPN)基质片剂,用于药物的持续释放。使用FTIR光谱检查IPN结构的配方,并通过FTIR,DSC和XRD分析评估药物与聚合物的相容性。研究了共聚物/ SAL比,药物载量和总聚合物/葡萄糖酸钙(CG)比对酸性和磷酸盐缓冲溶液中药物释放的影响。药物的释放是通过IPN基质的溶胀能力和聚合物溶解后形成的凝胶的粘度的相对大小来控制的。基质的溶胀能力取决于藻酸钙凝胶结构的形成和共聚物赋予的刚性。结果表明,PAam-g-SAL和SAL的IPN基质片剂可用于DTZ的缓释。

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