复方药物制剂的溶出度试验，通常采用定时取样，HPLC分离分析的办法解决。
Compound medicine preparation dissolution test usually adopt timing sampling method, such as HPLC, which split every composition from analytical solution.
方法：将度米芬渗透泵片在光照、高温、高湿条件下露置，定时取样，观察样品形态、含量及溶出度。
Methods: ODT was exposed to strong light, high temperature, high moisture of air respectively, and accelerating test was performed.
方法：制霉素甘油在不同光线及温度条件下放置，定时取样，采用HPL C法测定制霉素中三个主组分的含量。
METHOD: the contents of the three ingredients of nystatin glycerol after stored at different light and temperature were determined by HPLC.
方法：制霉素甘油在不同光线及温度条件下放置，定时取样，采用HPL C法测定制霉素中三个主组分的含量。
METHOD: the contents of the three ingredients of nystatin glycerol after stored at different light and temperature were determined by HPLC.
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