The dissolution rate was evaluated by similar factor method.
采用相似因子法对溶出度进行评价。
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。
Results Indicated there was a significant difference in dissolution rate.
结果不同厂家生产的产品溶出度有很大的差异。
OBJECTIVE: To study crospovidone effect on the dissolution rate of paracetamol tablets.
目的：研究崩解剂交联聚维酮对对乙酰氨酚片溶出度的影响。
Objective To prepare nifedipine solid dispersions and investigate their dissolution rate.
目的提高硝苯地平的体外溶出速率。
Aim To prepare Maodongqing sustained release pellet capsules and study the dissolution rate.
目的制备膜控释毛冬青缓释微丸胶囊并研究其体外释药性能。
The constant of dissolution rate was proportional to the square root of the disc rotation speed.
溶解速率常数是与圆盘转速的平方根成正比。
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。
Results: The software EXCEL was an efficient and exact way to process the data of dissolution rate.
结果：利用EXCEL软件能够有效、正确地处理溶出度实验数据。
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。
CONCLUSION Itraconazole solid dispersion can significantly increase it's solubility and dissolution rate.
结论：伊曲康唑固体分散体能明显提高伊曲康唑的溶解度及体外溶出速率。
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。
Because of discontinuity, chemical weathering can add water-rock interface and raise mineral dissolution rate.
由于非连续特性，化学风化可增大水岩界面，提升矿物溶解反应的规模及速率。
It is convenient feasible by self contrast method to determine the dissolution rate of Ginkgo biloba tablets .
自身对照法做为银杏叶片体外溶出度测定方法操作简便可行。
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。
OBJECTIVE To study the dissolution rate of fenoprofen calcium tablets and establish the quality control standard.
目的研究非诺洛芬钙片溶出度的方法学，为药品质量控制制定新的标准。
Surfactants increase the dissolution rate by increasing the wetability, solubility, and dispersibility of the drug.
表面活性剂通过增加药物的吸湿性、溶解度和分散性来增加其溶解速率。
Objective To determine extracorporeal dissolution rate of national dragon's blood capsule, and to control its quality.
目的比较不同厂家、不同批次盐酸胺碘酮胶囊的体外溶出度，为其质量控制提供依据。
But actually the operating result of the strategic alliance is not so satisfied. The dissolution rate is always higher.
但战略联盟的实际经营效果差强人意，联盟解散的比率一直较高。
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。
Methods: the software EXCEL was applied to process the data, calculate the parameters and draw the curve of dissolution rate.
方法：采用EXCEL软件对溶出度实验进行数据处理、参数计算及溶出曲线的绘制。
Indomethacin enteric dispersible tablets were prepared, and factors affected disintegration time and dissolution rate were studied.
制备了吲哚美辛肠溶分散片，考察辅料对其崩解时限及溶出速度的影响。
OBJECTIVE: To prepare the long acting nifedipine tablet, determined dissolution rate and plasma concentration of nifedipine in dog.
目的：制备硝苯地平缓释片并测定释放度和犬血药浓度。
The effect of confection process on medicine dissolution was examined by comparing the dissolution rate of Baicalin in tablet and pill.
比较片剂和丸剂中黄芩苷的溶出速率，考察成型工艺对药物溶出的影响。
OBJECTIVE: to prepare Radix Notoginseng total Saponin Dispersible tablets to enhance the dissolution rate and improve its absorbability.
目的：本实验制备了三七总皂苷分散片，以达到提高药物溶出，改善吸收。
The effect of heating temperature, holding time and cooling mode on its crystallizability and dissolution rate of potassium is not obvious.
改变合成温度、保温时间以及冷却方式等，对合成试样的结晶性能以及试样中钾元素溶出率的影响很小。
Objective: To test the dissolution rate of silymarin dropping pill as well as to be compared with other three commercial products of the silymarin.
目的：考察水飞蓟素滴丸的溶出度，并与市售水飞蓟素制剂进行比较。
OBJECTIVE To determine the dissolution rate of compound sulfamethoxazole tablets with the instrument of fiber-optic in situ dissolution testing (FODT).
目的研究光纤药物溶出度实时测定(FODT)仪监测复方磺胺甲恶唑片的溶出度。
Methods: Tretinoin in the dropping pills was determined spectrophotometrically and rotating basket method was adopted to determine its dissolution rate.
方法：采用紫外分光光度法测定滴丸中维甲酸的含量，转篮法考察其体外溶出度。
Methods: the solid dispersion was prepared by solvent method. The solubility, the dissolution rate and the derivative thermogravimetry (DTG) were determined.
方法：采用溶剂法制备固体分散体，进行溶解度、溶出速率测定，导数热重分析(DTG)。
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