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。
Using fluid bed coating equipment, the pellets was coated with HPMC. Results the results of dissolution test was good.
采用微型流化床包衣设备，将微丸包上HPMC薄膜衣，并测定了溶出度。
The dissolution test showed that they were accorded with the China Pharmacopia and quicker than that of the imported capsules.
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。
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。
Compound medicine preparation dissolution test usually adopt timing sampling method, such as HPLC, which split every composition from analytical solution.
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。
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。
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。
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。
In an analytic method for the calculation of parameters of the Weibull distribution is designed for dissolution test data of tablets. And the electronic computer program is also given.
本文对片剂溶出度的测定数据设计了以解析法求算威布尔分布参数的方法，并给出了电子计算机程序。
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。
This is quite an old test but there are several commercial devices available and is used on whole blood where it can measure clot formation and clot dissolution.
这是一项很老的检测方法，但是由一些可用的商品化设备组成，通过测量全血从而检测血栓形成和血栓溶解。
Normal manufacturer, ceramic cup through strict test, the lead cadmium dissolution is accord with a country compulsive standard, so is a safe and reliable.
正规厂家的陶瓷杯，都是经过严格检测的，其铅镉溶出是符合国家强制标准的，所以是安全可靠的。
Objective: To optimize the methods of test for the levofloxacin hydrochloride tablets dissolution.
目的：对盐酸左氧氟沙星片溶出度的试验方法进行优化。
A core evaluating test is conducted on the selected plugging agent, and its dissolution and temporary plugging intensity are detected.
对所筛选出的暂堵剂进行了岩心评价试验，对暂堵剂的溶解性及暂堵强度进行了测定。
A new soluble intravascular stent made of gelatin, a supplementary instrument of anastomosis, is devel-oped, and its dissolution rates in vascular anastomosis and the test in vitro are investigated.
目的：研制一种可溶性血管内支架辅助血管断端吻合，并检测该支架在血管吻合过程中的溶解性能。
Results:The test showed that the dissolution of calcium citrate malate is best, whenever the acidity of solution is negative, low, normal or high.
结果：果酸钙在无酸、低酸、正常胃酸及高酸条件下，均有良好的溶出结果。
The orthogonal test of the elements effecting electrode internal fluid and dissolution.
同时对影响电极内液及消解的因素进行正交实验确定最佳条件。
METHODS: By using circle basket test with paracetamol as the dissolution index, detected by UV, to abstract parameters and make correlation analysis.
方法：转篮法，以对乙酰氨基酚为溶出指标，用紫外分光光度法检测，提取参数，并对参数进行相关性分析。
Results the adhesive force, dissolution, buccal adhesive test and the clinical curative effect of the tablets were better than those of the films.
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。
Method the orthogonal test was used to optimize the preparation process of Herba Sarcandrae Buccal Tablet, palatability and dissolution time as the assessment index.
方法采用正交试验法，以含片的口感和溶出时限为指标，对含片的制备工艺进行优选。
This paper presents a method in which the content of calcium and barium all be measured with only one test specimen dissolution.
本文提出了一次溶样将钙、钡含量同时测定的方法。
This paper presents a method in which the content of calcium and barium all be measured with only one test specimen dissolution.
本文提出了一次溶样将钙、钡含量同时测定的方法。
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