Official USP dissolution testing 现行美国药典溶出度测试要求
以上来源于: WordNet
Objective: To establish a novel method for fully automated dissolution testing.
目的：建立新颖的自动化检测药物溶出度方法。
Through analysing the changes of gel beads before and after dissolution testing, the release mechanism of drug was studied.
比较凝胶小球在溶出前后的形态变化，进行药物释放机理的探讨。
If Stage 2 testing is rarely required, then an analytical alert for USP dissolution testing might be a single, unusual minimum or average dissolution.
如果很少要求第二阶段的测定，那么US P溶出度测定的分析警戒可能是一个单个的，非寻常最小值或平均溶出度。
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