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首页> 外文期刊>Journal of Pharmacy and Bioallied Sciences >Floating microspheres of valacyclovir HCl: Formulation, optimization, characterization, in vitro and in vivo floatability studies
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Floating microspheres of valacyclovir HCl: Formulation, optimization, characterization, in vitro and in vivo floatability studies

机译:伐昔洛韦HCl的漂浮微球:配方,优化,表征,体外和体内漂浮性研究

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Floating microspheres are multiple unit Gastroretentive drug delivery systems. Valacyclovir hydrochloride (VCH) is L-valyl ester prodrug of acyclovir. VCH degrades in intestinal fluid. The objective was to develop floating microspheres of VCH to localise the drug at upper part of GIT, for improved absorption. Floating microspheres were prepared by W/O emulsification solvent evaporation method using Ethylcellulose (EC) as polymer. Particle size and % EE were 550.021±0.241 μm, 79.88±2.236% respectively. in vitro and in vivo floatability studies confirmed floating behaviour of microspheres. VCH loaded floating microspheres can be a suitable alternative to the conventional formulation, by localizing the drug at upper GIT.KEY WORDS: Valacyclovir hydrochloride, microspheres
机译:漂浮的微球是多单位胃滞留药物递送系统。盐酸伐昔洛韦(VCH)是阿昔洛韦的L-戊酸酯前药。 VCH在肠液中降解。目的是开发VCH的漂浮微球,将药物定位在GIT的上部,以提高吸收率。使用乙基纤维素(EC)作为聚合物,通过W / O乳化溶剂蒸发法制备了漂浮的微球。粒度和%EE分别为550.21±0.241μm,79.88±2.236%。体外和体内漂浮性研究证实了微球的漂浮行为。载有VCH的漂浮微球可以通过将药物定位在GIT的上部来替代常规配方。关键词:盐酸伐昔洛韦,微球

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