Objective To assess the efficacy of new ultrasonic catheter for thrombus dissolution in vitro.
目的探讨新型超声导管体外消融血栓的可行性和疗效。
Objective:To Study the preparation and dissolution in vitro of salbutamol sulfate delayed -release tablets.
目的：解决硫酸沙丁胺醇延迟释放片定时释药问题。
Objective: To investigate the difference of dissolution in vitro of gatifloxacin in tablet and capsule from various manufacturers.
目的：探讨不同厂家加替沙星片剂与胶囊剂体外溶出度差异。
Results: The differences of dissolution in vitro of gatifloxacin in tablet and capsule from various manufacturers were significant.
结果：不同厂家加替沙星片剂与胶囊剂体外溶出度存在显著差异。
OBJECTIVE To study the dissolution rate in vitro of simvastatin pills.
目的探讨辛伐他汀滴丸的体外溶出速率。
The formulation, preparation process and dissolution rate in vitro of Sustained-Release Aspirin tablets(S-RAT)were studied.
本文研究了阿司匹林缓释片（S-RAT）的处方组成、制备工艺、体外溶出速率试验。
Objective To study the in vitro dissolution rate of levalbuterol hydrochloride sustained released tablets.
目的研究自制盐酸左旋沙丁胺醇缓释片的体外释放度。
The accumulative dissolution rate of puerarin in coprecipitates with different ratios of puerarin-phytosomes to PVP was investigated according to dissolution release in vitro.
以体外溶出度法考察不同配比PVP共聚物胶囊的药物累积溶出度。
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。
METHODS The dissolution of nimodipine in vitro was tested according to Chinese pharmacopoeia 2000, using the first method with RC dissolution tester.
方法按中国药典2000年版附录中转篮法测定尼莫地平片在人工胃液中的溶出度；
Conclusion: the dissolution method may be used to assess the drug delivery in vitro of methotrexate implants.
结论：所定方法可用于甲氨蝶呤植入剂的体外释放测试。
Objective: To compare dissolution rate of first-researching and imitating Ebastine tablets in vitro.
目的：比较原研和仿制药厂生产的依巴斯汀片的体外溶出度特性。
OBJECTIVE To prepare Shexiang Baoxin dispersible tablets and investigate the dissolution of borneol and total ginsenoside from them in vitro .
目的制备麝香保心分散片，考察冰片和人参总皂苷的体外溶出度。
Results: The in vitro dissolution rates of ISDN solid dispersion were faster than ISDN.
结果：固体分散体能加快药物的溶出速率，最佳比例为1∶7。
In vitro test of the rate of weight losses demonstrated that the dissolution of carbonated hydroxyapatite cement was better than the calcium phosphate cement.
失重率的检测表明，酸化羟基磷灰石骨水泥的失重率改变明显高于磷酸钙骨水泥。
Objective:To prepare the compound sophora alopecuroides suppository and determine its dissolution rate in vitro.
目的：制备复方苦豆子栓剂并测定其体外溶出度。
In vitro dissolution was more than 95%.
体外溶出度在达到95%以上。
The condition of preparation process, dissolution property in vitro, antibacterial activity in vitro and the sterilization experiment were studied.
考察了微球的制备条件，对其体外溶出、体外抑菌、灭菌实验进行了研究。
Objective: To develop a method for determining dissolution rate in vitro of Chuanxinlian tablets.
目的：建立穿心莲片的溶出度测定方法。
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。
Method: carvedilol solid dispersions were prepared by solvent-melting and coevaporation methods with PEG-6000 and PVP as carriers, the study on the dissolution was conducted in vitro.
方法：以聚乙烯吡咯烷酮（PVP）、聚乙二醇-6000（PEG-6000）为载体，溶剂法和溶剂熔融法制备固体分散体，并进行体外溶出度研究。
Dissolution test is an in vitro test method.
溶出度试验是一种体外检查方法。
The micromeritic properties, reception percentage and in vitro dissolution of pellets with different spheroniser load were determined.
考察了不同处方微丸的粉体学性质、收率和体外溶出度。
The in vitro dissolution profiles of salbutamol pulsatile pellets were fitted and compared by model fittingand model independent methods (difference factor method and similarity factor method).
比较了用模型拟合法和直接比较法（差异因子法和相似因子法）拟合不同处方硫酸沙丁胺醇脉冲微丸体外释放行为的情况。
AIM To establish a simple and effective method for assessing the dissolution of Ibuprofen's preparations in vitro.
摘要目的：建立一种简便有效的药物体外释放度测定方法。
OBJECTIVE: to study the dissolution rate in vitro of four tinidazole solid preparations produced by different domestic factories.
前言：目的：比较国内四个厂家生产的替硝唑固体制剂(片剂，胶囊剂)的体外溶出情况。
METHODS Preparing the solid dispersion by melting method at different drug-to-PEG ratios with different PEG moleculars and studying the preparation with dissolution rate in vitro and DSC method.
方法以不同分子量不同比例的聚乙二醇为载体，以熔融法制备固体分散体，并进行体外溶出度研究和DSC扫描。
Objective To examine the in vitro dissolution of chemical components of the coptis root powder of different granule diameters.
目的考察不同粒径黄连粉体化学成分体外溶出情况。
Conclusion: The dissolution rate of tanshinone in vitro can be improved with solvent deposition method.
结论：采用溶剂沉积法提高丹参酮的体外溶出度是可行的。
OBJECTIVE to optimize preparation techniques for puerarin phytosomes and explore their solid dispersions to increase the dissolution of puerarin in vitro.
目的优化葛根素磷脂复合物的制备工艺，研究其固体分散体，提高葛根素的体外溶出速率。
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