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Fabrication and evaluation of propranolol hydrochloride loaded microspheres by ionic-gelation technique

机译:离子凝胶技术制备盐酸普萘洛尔微球的制备与评价

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The aim of present research work was to formulate and evaluate microspheres of Propranolol Hydrochloride to achieve sustained release system using combination of algino- eudragit RS100 system by ionic-gelation technique. The prepared microspheres were evaluated for various parameters like percentage yield, particle size, flow property, entrapment efficiency, surface study, in-vitro drug release, X-Ray diffraction analysis, etc. It was found that all formulations showed improved flow behavior as compared to pure drug, it was observed that on increasing the polymer concentration of formulations the entrapment efficiency and particle size were increased. The surface morphology study by SEM indicated that microspheres were spherical with rough outer surface. There was no interaction between the drug and the polymers, as studied by FTIR study. In-vitro drug release study showed that on microsphere formulation its release was sustained and its release was affected by polymer concentration and it followed Higuchi model. Therefore, it can be concluded that Propranolol Hydrochloride loaded algino-eudragit RS100 microspheres can be formulated for sustained drug delivery of Propranolol Hydrochloride.
机译:目前研究工作的目的是通过离子胶凝技术,结合al-eudragit RS100系统配制和评估盐酸普萘洛尔微球以实现缓释系统。对制备的微球进行了各种参数的评估,例如百分产率,粒径,流动性,包封效率,表面研究,体外药物释放,X射线衍射分析等。发现与所有的制剂相比,所有制剂均表现出改善的流动性对于纯药物,观察到随着制剂聚合物浓度的增加,包封效率和粒径增加。 SEM的表面形态研究表明,微球为球形,外表面粗糙。 FTIR研究表明,药物与聚合物之间没有相互作用。体外药物释放研究表明,在微球制剂中,其释放得以持续,并且其释放受到聚合物浓度的影响,并且遵循Higuchi模型。因此,可以得出结论,可以将载有盐酸普萘洛尔的algo-eudragit RS100微球配制成用于盐酸普萘洛尔的持续药物递送。

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