The USP tablet dissolution test is an analytical tool used for the verification of drug release processes and formulation selection within the pharmaceutical industry.
USP规定的片剂溶出试验被广泛用于医药工业中药物释放过程的验证和处方筛选。
For example, consider the three-stage USP dissolution test.
例如，USP中溶出度的三阶段测定。
The system was used for dissolution test of isoniazid tablets.
该系统用于异烟肼片的溶出度测定。
Conclusions This method can be used for dissolution test of bendazol tablets.
结论：本方法适用于地巴唑片的溶出度测定。
Objective To establish an accurate method for dissolution test of cyproterone acetate tablets.
目的建立准确测定复方醋酸环丙孕酮片溶出度的方法。
The dissolution test for itraconazole hydrochloride capsules by UV spectrometry was presented.
建立了盐酸伊曲康唑胶囊溶出度的紫外分光光度测定法。
It suggests that we should take the real-time dissolution test to ensure the intrinsic quality of medicines and drug safety and efficacy.
有必要进行制剂溶出度的实时监测，确保药品的内在质量，保证用药的安全性及有效性。
Objective dissolution test was applied to study the dissolution rates of total flavones from Pollen Typhae before and after wall breaking.
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。
UV analytical method on dissolution test of betaxolol hydrochloride tablets was developed, and the dissolution curve of the tablets were also studied.
建立了盐酸倍他洛尔片溶出度的UV测定方法，并研究了盐酸倍他洛尔片的溶出曲线。
Comparing the difference of the dissolution of gliquidone tablets by fiber-optic dissolution test system which use two different standard curve equations.
使用光纤药物溶出仪应用两种标准曲线方程时，比较格列喹酮片的溶出度差异。
OBJECTIVE To establish process analysis method for the dissolution test of aminophylline tablets by fiber optic chemical sensor dissolution test system (FOCSDT-6).
目的：在自行研制的六通道溶出度过程分析系统上建立药物溶出度自动监测技术。
Methods Screening the optimal formulation of liquid type carrier was carried out through measuring apparent solubility in different solvent and dissolution test in vitro.
方法通过不同溶剂中的溶解度实验及体外溶出度实验，筛选并优化处方。
The identification, determination and dissolution test results of three batches of Yiganqing sustained tablets demonstrated that the producing process is feasible and stable.
三批产品的鉴别、含量测定和释放度考察结果表明本制剂工艺的重现性和稳定性良好。
Conclusion: it is very difficult to characterize the dissolution rate and control the dissolution performance and inherent quality of sustained-release preparation by a single-point dissolution test.
结论单点溶出度测定方法不能真正反映出缓释制剂的溶出速率，难以控制其溶出性能与内在质量。
Conclusion: it is very difficult to characterize the dissolution rate and control the dissolution performance and inherent quality of sustained-release preparation by a single-point dissolution test.
结论单点溶出度测定方法不能真正反映出缓释制剂的溶出速率，难以控制其溶出性能与内在质量。
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