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盐酸尼卡地平缓释微丸的制备
引用本文:原丽慧,卞俊. 盐酸尼卡地平缓释微丸的制备[J]. 药学实践杂志, 2013, 31(4): 258-261
作者姓名:原丽慧  卞俊
作者单位:1. 解放军第411医院药学科,上海200434;江西中医学院药学院,江西南昌330004
2. 解放军第411医院药学科,上海,200434
摘    要:目的 制备盐酸尼卡地平缓释微丸,并考察其体外释药的影响因素.方法 采用底喷式流化床包衣法,以空白丸芯为基础制备速释微丸,乙基纤维素水分散体为包衣材料制备盐酸尼卡地平缓释微丸,考察其包衣处方及工艺的影响因素.结果 所得缓释微丸在2、6、12h的累积释药百分率分别为24%、69%、87%,体外释放曲线符合一级方程.结论 制备的微丸缓释效果理想,且制备工艺简单,操作方便.

关 键 词:盐酸尼卡地平  乙基纤维素水分散体  缓释微丸  流化床
收稿时间:2012-09-04
修稿时间:2013-04-08

Preparation of nicardipine hydrochloride sustained-release pellets
YUAN Li-hui and BIAN Jun. Preparation of nicardipine hydrochloride sustained-release pellets[J]. The Journal of Pharmaceutical Practice, 2013, 31(4): 258-261
Authors:YUAN Li-hui and BIAN Jun
Affiliation:Department of Pharmacy, 411th Hospital of PLA, Shanghai 200434, China and Department of Pharmacy, 411th Hospital of PLA, Shanghai 200434, China
Abstract:Objective To prepare nicardipine hydrochloride sustained-release pellets and investigate the influencing factors of the drug release in vitro. Methods The rapid-release pellets were prepared by fluidized bed coating method based on blank pill core and then nicardipine hydrochloride sustained-release pellets were prepared with surelease. The factors to influence the drug release behaviors and their properties were evaluated. Results The release percentage of the sustained-release pellets could be controlled by 24%, 69%, 87% at 2 h, 6 h, 12 h respectively, the drug release mechanism in vitro followed first-order equations.Conclusion The pellets showed an obviously sustained-release effect.The preparation process was simple and convenient.
Keywords:nicardipine hydrochloride  surelease  sustained-release pellets  fluidized bed
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