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盐酸维拉帕米脉冲释放片体内外释药特性
引用本文:范辉,周晗瑛,梁文权. 盐酸维拉帕米脉冲释放片体内外释药特性[J]. 中国医院药学杂志, 2002, 22(5): 271-274
作者姓名:范辉  周晗瑛  梁文权
作者单位:1. 浙江医科大学附属邵逸夫医院,浙江,杭州,310016
2. 浙江大学药学院,浙江,杭州,310006
摘    要:
目的:研究盐酸维拉帕米脉冲释放片体内外释药特性。方法:用干法压制包衣技术制备盐酸维拉帕米脉冲释放片,调整包衣中致孔剂用量,通过体外释放度试验考查时滞,并用HPLC法测定家兔血药浓度,考查体内外时滞的相关性。结果:体内外时滞基本相符。结论:可用体外时滞预测体内的时滞。

关 键 词:盐酸维拉帕米脉冲释放片 体内外释药特性 干压包衣片 时滞 心血管系统药
文章编号:1001-5213(2002)05-0271-04
修稿时间:2001-08-29

Study on the in vitro and in vivo drug release of verapamil hydrochroride pulsatile release tablet
FAN Hui,ZHOU Han Ying,LIANG Wen Quan. Study on the in vitro and in vivo drug release of verapamil hydrochroride pulsatile release tablet[J]. Chinese Journal of Hospital Pharmacy, 2002, 22(5): 271-274
Authors:FAN Hui  ZHOU Han Ying  LIANG Wen Quan
Abstract:
OBJECTIVE To study the in vitro and in vivo drug release of verapamil hydrochloride pulsatile release tablet.METHODS Verapamil hydrochroride pulsatile release tablet was prepared using convenient dry coating techniques. A high performance liquid chromatography method was used to determine the plasma concentration of rabbits. The in vitro in vivo correlation was evaluated.RESULTS There was a good correlation between in vitro and in vivo lag time.CONCLUSIONS The in vivo lag time can be well predicated by in vitro value.
Keywords:verapamil hydrochloride  pulsatile release system  dry coated tablet  lag time  controlled release
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