Controlled release of diclofenac sodium from sodium alginate beads crosslinked with glutaraldehyde1

Anandrao R Kulkarni, Kumaresh S Soppimath, Tejraj M Aminabhavi
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引用次数: 123

Abstract

Controlled release sodium alginate (Na–Alg) beads containing diclofenac sodium (DS) have been prepared by precipitation of Na–Alg in alcohol followed by crosslinking with glutaraldehyde (GA) in acidic medium. Preparation of the beads was optimized by considering the percentage entrapment efficiency, swelling capacity of beads in water and their release data. The percentage entrapment efficiency was found to vary between 30 and 71 depending upon the conditions of their preparations. The beads produced at higher temperatures and longer times of exposure to the crosslinking agent have shown the lower entrapment efficiency, but extended release of DS from the beads. The scanning electron microscopic studies indicated nonporous smooth surfaces and the differential scanning calorimetric data indicated the molecular level dispersion of the drugs in the beads.

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戊二醛交联海藻酸钠微球双氯芬酸钠的控释研究
以双氯芬酸钠(DS)为原料,用Na-Alg在醇中沉淀,并与戊二醛(GA)在酸性介质中交联,制备了海藻酸钠(Na-Alg)控释微球。综合考虑微球的包封率、在水中的溶胀量以及微球的释放性能,对微球的制备工艺进行了优化。根据其制备条件的不同,捕集率在30%至71%之间变化。在较高的温度和较长的交联时间下制备的微球的包封效率较低,但DS的释放时间较长。扫描电镜研究表明,微球表面光滑无孔,差示扫描量热数据表明,药物在微球中的分子水平分散。
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