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复方妇炎康栓的制备及质量控制
引用本文:李爱英,熊南燕,姜彩娥.复方妇炎康栓的制备及质量控制[J].中国药房,2004,15(4):219-221.
作者姓名:李爱英  熊南燕  姜彩娥
作者单位:1. 河北邯郸医专附属医院,邯郸市,056029
2. 河北邯郸市第一医院,邯郸市,056001
摘    要:目的:制备复方妇炎康栓剂并建立其质量标准、方法:以替硝唑、呋喃西林等为主药制备栓剂;以高效液相色谱法控制含量。结果:复方妇炎康栓中替硝唑和呋喃西林分别在192.0 480μg/ml~448.1 120μg/ml(r替=0.9 999)和9.6 672μg/ml~22.5 568μg/ml(r呋=0.9 998)浓度范围内线性关系良好;平均回收率分别为100.37%、101.45%,相对标准差分别为1.171%(n=5)、1.771%(n=5)。结论:复方妇炎康栓性质稳定,质量控制方法简便,含量测定准确、可靠。

关 键 词:复方妇炎康栓  制备  质量控制
文章编号:1001-0408(2004)04-0219-03
修稿时间:2003年4月1日

Preparation and Quality Control of Compound Fuyankang Suppository
LI Aiying.Preparation and Quality Control of Compound Fuyankang Suppository[J].China Pharmacy,2004,15(4):219-221.
Authors:LI Aiying
Abstract:OBJECTIVE: To prepare the compound Fuyankang suppository and establish the quality control method. METHODS :Funancillin and Tinidazole were used to prepare compound Fuyankang suppository and HPLC method was established for content determination of funancillin and Tinidazole in the suppository .RESULTS: The standard curves of fu-nancillin and Tinidazole were linear in the ranges of (9.6672-22.5 568)μg/ml(r = 0.9 998, n = 5) and (192.048-448.112) μg/ml(r = 0.9 999,n= 5)and the average recoveries were 101.45% and 100.37% with RSD 1.771%(n= 5) and 1.177%(n = 5) respectively .CONCLUSION: The suppository is stable in quality.The method of determination of the contents is simple, rapid and reliable.
Keywords:compound Fuyankang suppository  preparation  quality control
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