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法莫替丁分散片的研制及体外溶出特性
引用本文:张建春,王原,陈鼎继,王春宏,温亚旭.法莫替丁分散片的研制及体外溶出特性[J].中国药房,2002,13(8):473-474.
作者姓名:张建春  王原  陈鼎继  王春宏  温亚旭
作者单位:解放军第一医院药剂科,兰州市730030
摘    要:目的 :研制法莫替丁分散片 ,并考察其体外溶出特性。方法 :采用正交设计方法优选出制备的最佳条件。结果 :本品在1min内可完全崩解 ;体外溶出度表明 ,T50=0 56min。结论 :用优选处方制备的法莫替丁分散片比市售片崩解快 ,分散均匀。

关 键 词:法莫替丁  分散片  正交设计  溶出度
文章编号:1001-0408(2002)08-0473-02
修稿时间:2001年10月8日

Preparation and in Vitro Dissolution Characteristics of Famotidine Dispersible Tablets
ZHANG Jianchun,WANG Yuan,CHEN Dingji,WANG Chunhong,WEN Yaxu.Preparation and in Vitro Dissolution Characteristics of Famotidine Dispersible Tablets[J].China Pharmacy,2002,13(8):473-474.
Authors:ZHANG Jianchun  WANG Yuan  CHEN Dingji  WANG Chunhong  WEN Yaxu
Abstract:OBJECTIVE:To study the preparation of famotidine dispersible tablets and to observe the dissolution characteristics in vitro METHODS:To optimize the conditions for preparation by orthogonal design RESULTS:The tablets could completely disintegrate within 1 min;In vitro dissolution test showed T50=0 56min CONCLUSION:In comparison with commercial famotidine tablets,the dispersible tablets prepared in optimum condition were rapid in disintegration and homogenous in dispersal
Keywords:famotidine  dispersible tablet  orthogonal design  dissolubility
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