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Formulation and evaluation of ethyl cellulose microspheres prepared by the multiple emulsion technique.

机译:通过多重乳液技术制备的乙基纤维素微球的配制和评估。

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The aim of this study was to formulate and evaluate microencapsulated controlled release preparations of metformin hydrochloride using ethyl cellulose as the retardant material with high entrapment efficiency and extended release. Microspheres were prepared by the double emulsion solvent diffusion method. A mixed solvent system consisting of acetonitrile and dichloromethane in 1:1 ratio and light liquid paraffin were chosen as the primary and secondary oil phases, respectively. Span 80 was used as the surfactant for stabilizing the secondary oil phase. The prepared microspheres were characterized by drug loading, optical microscopy and scanning electron microscopy (SEM). The in vitro release studies were performed in a series of buffer solutions with variable pH. The drug loaded microspheres showed 55-85% of entrapment and the release was extended for up to 12 h. SEM studies revealed that the microspheres were spherical and porous in nature. Data obtained from in vitro release studies were fitted to various kinetic models and high correlation was obtained with the Higuchi model. The drug release was found to be diffusion controlled. Oral administration of the microspheres to the albino mice provided decreased plasma glucose for more than 10 h.
机译:本研究的目的是使用乙基纤维素作为缓释材料,以高包封率和缓释作用,配制和评价盐酸二甲双胍的微囊控释制剂。通过双乳液溶剂扩散法制备微球。选择分别由1:1比例的乙腈和二氯甲烷和轻质液体石蜡组成的混合溶剂系统作为一级和二级油相。跨度80用作稳定第二油相的表面活性剂。制备的微球通过载药,光学显微镜和扫描电子显微镜(SEM)表征。在一系列pH可变的缓冲溶液中进行了体外释放研究。载药微球显示出55-85%的包封,并且释放延长长达12小时。 SEM研究表明,微球本质上是球形和多孔的。从体外释放研究中获得的数据适合各种动力学模型,并与Higuchi模型获得高度相关性。发现药物释放受扩散控制。对白化病小鼠口服微球可降低血浆葡萄糖超过10小时。

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