不同释放度测定方法没有明显差别；
The results of different methods measuring release percentage had no obvious difference.
摘要目的：建立一种简便有效的药物体外释放度测定方法。
AIM To establish a simple and effective method for assessing the dissolution of Ibuprofen's preparations in vitro.
目的建立罗通定缓释片体外释放度测定方法，评价其体外释药行为。
Objective to establish a UV method to determine the release degree of rotundine sustained-release tablets and to evaluate its in-vitro release behavior.
本制剂的质量标准研究主要包括有关物质检查、含量测定和释放度测定。
The research of quality criteria include inspections of relevant substance, the assaying and the releasing in vitro.
目的建立肺靶向阿霉素明胶微球（ADM-GMS）体外释放度测定的方法。
Objective To establish a method for the analysis of release rate in vitro of adriamycin in adriamycin gelatin microspheres(ADM-GMS).
结论本释放度方法简单，快速，可用于盐酸二甲双胍缓释片体外释放度测定。
Conclusions the determination method is simple and swift, and can be applied in the determination of in vitro release rate of metformin hydrochloride sustained-release tablets.
目的：建立复方丹参缓释片多指标成分的体外释放度测定方法，评价其体外释药行为。
Objective: to develop the methods to determine the in vitro release of multi-target ingredients in Compound Danshen Sustained-release Tablets and to evaluate its release behavior in vitro.
结论方法结果准确，不受制剂中辅料的干扰，适用于格列吡嗪缓释胶囊的释放度测定。
CONCLUSION the method is an accurate for the drug release determination of Glipizide Sustained release Capsules, the analysis is out of interference of excipients.
逸出值测试在正是要评估产品的变异性的情况下不适用，如含量均一性，溶解度，释放率测定。
Outlier tests have no applicability in cases where the variability in the product is what is being assessed, such as for content uniformity, dissolution, or release rate determinations.
方法：用高分子化合物作辅料制备缓释片，测定释放度。
METHODS High molecule polymer excipient was used in the process and release rate was determined.
方法：用高效液相色谱法与紫外分光光度法分别同时测定利福平胃溶胶囊的溶出度与利福平微丸胶囊的释放度。
Method: To determine the dissolution of the rifampicin gastric capsules by UV spectrum method and the release of rifampicin micro pill capsules by HPLC respectively.
采用HPLC法测定微球的体外释放度。
目的测定硝酸甘油贴膜的含量均匀度和体外释放度。
Objective To determine the content uniformity and controlled release characteristics of transdermal nitroglycerin in vitro.
方法：采用液中固化法制备果胶钙骨架型小丸并优化其工艺参数，以紫外分光光度法测定其体外释放度。
METHODS Rutin calcium pectinate pellets were prepared by in-liquid solidifying method, the best parameters were chosen and its release properties in different media was evaluated.
结论药品测定溶出度或释放度时，应先考察溶出度测定仪的自动取样装置对其是否有吸附作用，否则影响测定结果。
CONCLUSION the adsorption should be tested when automatic sampling device is used to determine dissolution and releasing degree for different drugs, or the results of determination might be affected.
方法 两步压片法压制脉冲片，荧光分析法测定脉冲片体外释放度值。
The release degree of salbutamol impulse tablet was determined by fluorescence analytical method in vitro.
建立了紫外分光光度法，用于盐酸氯米帕明基本理化性质、片剂释放度和含量的测定；
According to the literature, UV spectrophotometry was developed for the investigation of physicochemical properties, content and drug release in vitro.
目的：建立双黄补牙周缓释药条的质量控制标准，并测定其体外释放度。
OBJECTIVE To establish a quality standard for Shuanghuangbu sustained release periodontal medicinal strip and investigate its in vitro drug release.
目的：制备硝苯地平缓释片并测定释放度和犬血药浓度。
OBJECTIVE: To prepare the long acting nifedipine tablet, determined dissolution rate and plasma concentration of nifedipine in dog.
本方法准确，快速，简便，可用于复方胶原蛋白烧伤膜释放度的测定。
This method is accurate, rapid and simple for the quality control of the collagen burn pellicle of compound sulfadiazine silver.
方法：通过测定颗粒的可压性和片剂释放度来评价并确定制备工艺。
METHODS: to evaluate and set the manufacturing process according to the compressibility of the granule and the dissolubility of the finished tablets.
方法：以紫外分光光度法测定自制尼莫地平缓释片的释放度。
Methods: the releasing effect was measured by the ultraviolet spectrophotometry.
应用自制的透皮释放扩散池装置进行透皮释放度研究，高效液相色谱法测定释放液中黄芩苷的含量。
The transdermal release was determined by a self-designed diffusion cell system, and the content of baicalin was detected by HPLC.
采用浆法测定释放度，考察其释放行为。
方法采用小杯法测定LDAET的释放度。
METHODS The cup method was used to determine the dissolution of LDAET.
方法采用小杯法测定LDAET的释放度。
METHODS The cup method was used to determine the dissolution of LDAET.
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