摘要
目的:建立保泰松片溶出度的检测方法。方法:从溶出方式、溶出介质、转速3个因素考察,紫外分光光度法测定,对不同厂家批次的保泰松片的溶出曲线进行对比研究。结果:采用桨法,以pH6.8磷酸盐缓冲液为溶出介质,转速为100 r·min-1,考察市售保泰松片的溶出度。结论:此方法准确、可靠,可用于评价保泰松片的质量。
Objective:To establish a method for the dissolution determination of phenylbutazone tablets.Methods:Comparison of dissolution curves for different batches of phenylbutazone tablets was presented by UV spectrophotometry with three factors,including the dissolution mode,medium and speed.Results:The dissolution determination conditions of phenylbutazone tablets were as follows:an oar method was used with the stiring speed of 100 r · min-1,and the dissolution medium was pH 6.8 phosphate buffer.Conclusion:The method is accurate and reliable,and can be used to evaluate the quality of phenylbutazone tablets.
出处
《中国药师》
CAS
2014年第6期962-964,共3页
China Pharmacist
基金
安徽省科研课题(编号:.10021303018)
关键词
保泰松片
溶出度
质量评价
Phenylbutazone tablets
Dissolution
Quality evaluation