摘要
本文用紫外分光光度法对9个厂家27个批号的阿斯匹林肠溶衣片和复方新诺明片进行了体外溶出度测定。经F 检验和t 检验表明,约有60%的阿斯匹林肠溶衣片和35%的复方新诺明片能达到有关标准。
The dissolution of 27(?)lots of aspirin enteric-coated tablet and SMZ Co.Tabletmade by 9 factories was determined with ultraviolet spectrophotometry.theresults of F-test and t-test the results of indicated that 60% of Aspirin enteric-coated tablet and 35% of SMZ Co.tablet could comply with the requirements ofthe specificati ous.
出处
《中国医院药学杂志》
CAS
CSCD
北大核心
1990年第8期342-344,共3页
Chinese Journal of Hospital Pharmacy
关键词
溶出度
光度法
阿斯匹林
新诺明
Dissolution test
Ultraviolet spectrophotometry
Aspirin Compound tablet of SMZ
