溶出度试验是一种体外检查方法。
目的：建立能够区分西咪替丁片剂中不同晶型的溶出度试验法。
Objective:To establish a dissolution method to distinguish polymorphism A and B of cimetidine tab-lets.
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.
溶出度试验结果表明微粉化片溶出度达到中国药典普通片质量要求，比进口胶囊剂溶出速度快。
The dissolution test showed that they were accorded with the China Pharmacopia and quicker than that of the imported capsules.
目的对破壁前后的蒲黄进行溶出度试验，考察破壁工艺对蒲黄中有效成分总黄酮溶出速率的影响。
Objective dissolution test was applied to study the dissolution rates of total flavones from Pollen Typhae before and after wall breaking.
目的：对盐酸左氧氟沙星片溶出度的试验方法进行优化。
Objective: To optimize the methods of test for the levofloxacin hydrochloride tablets dissolution.
验证试验表明，响应面优化后得到猕猴桃果浆出汁率、果汁澄清度和乙醇不溶物回归方程的相关系数分别为0.958、0.904和0.922。
Demonstration tests indicated that the R values of juice yield, clarity and alcohol insoluble solid equations were 0.958, 0.904 and 0.922 respectively.
结果粘附片剂的粘附力、溶出度、口腔内粘附试验及临床疗效均比粘附膜剂优越。
Results the adhesive force, dissolution, buccal adhesive test and the clinical curative effect of the tablets were better than those of the films.
方法：采用高效液相色语-紫外检测法为测定影响因素试验、加速试验及室温留样条件下的稳定性和溶出度。
METHODS: HPLGUV was used to determine the stability and dissolution of the samples to be laid in the condition of severe test, accelerated test and long-term storage test.
方法：采用高效液相色语-紫外检测法为测定影响因素试验、加速试验及室温留样条件下的稳定性和溶出度。
METHODS: HPLGUV was used to determine the stability and dissolution of the samples to be laid in the condition of severe test, accelerated test and long-term storage test.
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