Design and Characterization of Sustained Released Alginate Beads of Meclizine Hydrochloride

Wajid Ahmad, Rihan Jawed
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引用次数: 2

Abstract

The objective of present study was to prepare alginate beads of antihistamine meclizine hydrochloride for sustain release action. The alginate beads were prepared by employing sodium alginate as a polymer with sodium carboxymethyl cellulose and chitosan hydrochloride as release retardant. The method of preparation employed was ionotropic gelation. The prepared beads were seen having the drug release rate of 98.34% of A4 batch and 99.02% of B4 batch in the time period of 12hrs. The maximum percent drug content of 94.72±0.06% was found in A4 batch. From the results it can be seen that A4 batch was found to be optimum as it was having maximum drug content and maximum amount of drug release in the predicted time period of 12hrs. The microbeads of meclizine hydrochloride by using ionotropic gelation method were prepared successfully employing various polymers in different concentrations. The prepared microbeads can be a better alternative than various other sustained release dosages forms.
盐酸美甲嗪海藻酸盐缓释微球的设计与表征
本研究的目的是制备具有缓释作用的抗组胺药盐酸美甲嗪海藻酸酯微球。以海藻酸钠为聚合物,羧甲基纤维素钠和盐酸壳聚糖为缓释剂,制备了海藻酸钠微球。采用离子化凝胶法制备。在12小时内,A4批和B4批的释药率分别为98.34%和99.02%。其中,A4批含药率最高,为94.72±0.06%。从结果可以看出,A4批在预测时间12hrs内药物含量和释放量最大,为最佳。采用不同浓度的聚合物,采用离子化凝胶法制备了盐酸美氯嗪微球。所制备的微珠是一种比其他各种缓释剂型更好的替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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