舒必利片溶出度考察  

Study on the Dissolution Test for Sulpride Tablets Prepared by Different Manufacturers

作　　者：瞿发林[1] 丁青龙[1] 殷强[2] 

机构地区：[1]中国人民解放军一○二医院,常州213003 [2]常州市药品检验所

出　　处：《中国医院药学杂志》1991年第5期209-211,共3页Chinese Journal of Hospital Pharmacy

摘　　要：本文采用紫外法对国产五个厂舒必利片进行溶出度测定。求得的T50、Td参数具有显著性差异(P<0.01),提示国产舒必利片有必要把溶出度测定作为其质量控制标准之一。The dissolution of five batches of Sulpride tablets. from five domestic Pharma-ceutical factories was determined by UV.Td and T_(50) were very significant(P<0.01)It was demonstrated that the dissolution test of Sulpride tablet should be speci-fied in its standard of quality control.

关 键 词：舒必利 溶出度 紫外法 

分 类 号：R927.11[医药卫生—药学]