医院药师与药学院合作开展仿制药评价——以洛索洛芬钠片溶出度试验为例

Tazuko Ogawa, Naoshi Osawa, T. Uchida, K. Matsuyama
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引用次数: 4

摘要

我们选择了八种loxoprofen钠(一种非甾体抗炎药)的仿制药,并使用JP XIII中描述的桨叶法检测了这些药物的溶出能力。在100转/分、37℃条件下对第一种溶液(pH为1.2的解离试验溶液)进行溶出度测试时,发现先锋药物(A片)在15 min内完全溶解。一些仿制药的溶出度与先锋药物几乎相同,只有一种仿制药(F片)的溶出度较慢,在15 min内释放63.8%。使用第一种溶液在50 rpm和37°C下进行溶出试验。因此,F片剂没有达到卫生和福利部规定的最低要求。上述溶出度试验由作者在武川女子大学药学院药物学实验室进行。今后应大力鼓励医院药师与药学院校开展合作,开展仿制药评价工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Collaboration of Hospital Pharmacists with Pharmaceutical College on Evaluation of Generic Drugs : The Case of Dissolution Test of Sodium Loxoprofen Tablets
We selected eight generic drugs of sodium loxoprofen, a nonsteroidal anti-inflammatory drug (NSAID), and examined the dissolution ability of these drugs using the paddle method described in JP XIII.When performing the dissolution test performed on the 1st solution (disintengration test solution, pH 1.2) under the condition of 100 rpm and 37°C, the pioneer drug (Tablet A) was found to completely dissolve within 15 min. Some generic drugs showed almost the same dissolution profiles as the pioneer drug, whereas only one generic drug (Tablet F) showed a slower dissolution profile, a 63.8% release within 15 min.Furthermore, for Tablet A and Tablet F, the dissolution test using the 1st solution was performed at 50 rpm and 37°C. As a result, tablet F did not meet the minimum requirement established by the Ministry of Health and Welfare.The above dissolution tests were performed by the authors at the pharmaceutical laboratory of the School of Pharmaceutical Sciences, Mukogawa Women's University. Such collaboration by pharmacists in hospitals with pharmaceutical college in order to evaluate generic drugs should be more strongly encouraged in the future.
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