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。
OBJECTIVE: To improve the dissolubility and dissolution rate of carvedilol.
目的：制备卡维地洛固体分散体，提高其溶解度和溶速率。
Objective To establish the assay method of dissolution rate on Acipimox Capsules.
目的确立阿昔莫司胶囊溶出度测定方法。
Conclusion Etodolac solid dispersion can significantly increase the dissolution rate.
结论依托度酸固体分散体能显著提高依托度酸的溶出速率。
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: 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。
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。
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。
OBJECTIVE: To study on the dissolution rate of Suxiao Shangfeng capsule in order to evaluate the capsule quality.
前言： 目的：测定速效伤风胶囊的溶出速率。
OBJECTIVE To prepare dimenhydrinate (DMH) orally disintegrating tablets with fast dissolution rate and good taste.
目的制备既可掩盖苦麻味又能快速崩解的茶苯海明口腔崩解片。
Conclusion: The Phellinus linteus polysaccharides dispersible tablets with the high dissolution rate were achievable.
结论： 所制备的桑黄多糖分散片制备工艺简单，崩解快，性质稳定，具有实用价值。
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。
CONCLUSION The dissolution rate of NFDP can be improved greatly by solid dispersions with proper ratio of drug and carrier.
结论药物与载体合适比例的固体分散物明显提高其体外溶出速率。
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。
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。
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 The solid dispersion method was adopted to enhance the dissolution rate of nifedipine (NFDP) which is a poorly water-soluble drug.
目的采用制剂技术提高难溶性药物硝苯地平体外溶出速率。
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