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乳酸依沙吖啶凝胶的制备及质量控制
引用本文:曾德贵.乳酸依沙吖啶凝胶的制备及质量控制[J].中国药业,2006,15(10):34-35.
作者姓名:曾德贵
作者单位:广东省深圳市慢性病防治院,广东,深圳,518020
摘    要:目的研究乳酸依沙吖啶凝胶制备及质量控制方法。方法用卡波姆为主要基质制备乳酸依沙吖啶凝胶,采用紫外分光光度法在362nm波长处测定主药含量。结果含量测定方法平均回收率为100.32%,RSD=0、37%,样品卫生学检查符合规定,凝胶稳定无变化。结论该制剂制备工艺简单,质量可靠。

关 键 词:乳酸依沙吖啶  凝胶剂  制备  质量控制
文章编号:1006-4931(2006)10-0034-02
收稿时间:03 24 2006 12:00AM
修稿时间:2006年3月24日

Preparation and Quality Control of Ethacridine Lactate Gel
Zeng Degui.Preparation and Quality Control of Ethacridine Lactate Gel[J].China Pharmaceuticals,2006,15(10):34-35.
Authors:Zeng Degui
Institution:Hospital of Chronic Disease in Shenzhen, Guangdong Province, Shenzhen, Guangdong, China 518020
Abstract:Objective To develop a gel of ethacridine and the methods of quality control. Methods Using carbomer as the gel strome, the gel of ethaeridine lactate was developed. Results In the test of content, the average recovery rate was 100.32% and RSD=0.37%, It qualified the standard through the hygienieal test, After going through the eentrifugation in high speed, no change in the gel was found. Conclusion The gel can be easily developed, The quality is able to be controlled.
Keywords:ethacridine lactate  gel  preparation  quality control
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