采用HPLC法测定微球的体外释放度。
目的：制备地红霉素微囊并考察其体外释放度。
Objective: to prepare the microcapsules of dirithromycin and to study its release rate in vitro.
并以黏附力、体外释放度两个指标筛选优化处方。
The formulation was optimized using adhesive force and in vitro release as two evaluation parameters.
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.
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 study the in vitro dissolution rate of levalbuterol hydrochloride sustained released tablets.
目的考察硫酸长春新碱脂质体的体外释放度及其药效。
Objective To investigate the release rate and pharmacodynamics in vitro of of vincristine sulfate liposomes.
前言：目的：研究盐酸氨溴索渗透泵控释片的体外释放度。
Objective: To study the in vitro release rate of ambroxol HCl osmotic pump controlled release tablets.
目的对盐酸二甲双胍缓释片体外释放度相关因素进行研究。
Objective to study on the factors involved in the release rate of metformin hydrochloride in vitro sustained-release tablets.
目的制备葛根素肠溶纳米粒，并对其体外释放度进行考察。
Aim To prepare puerarin enteric nanoparticles and investigate their release rate in vitro.
结果：PLGA相对分子质量对微球体外释放度影响较大。
Results: the effect of the molecular weight of PLGA on in vitro release rate was evident.
目的：制备苦参总碱肠溶片，并建立体外释放度分析方法。
Objective: Alkaloids of sophora flavescens enteric-coated tablets was developed, and the method of drug release was established.
方法进行体外释放度实验，考察释放介质对释放度的影响。
METHODS Experiment of release rate in vitro was carried on and medium effects upon the release were investigated.
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.
目的考察麝香保心p H依赖型梯度释药微丸的体外释放度。
Object To investigate the release of pH dependent gradient releasing heart protecting musk pellets (GRHPMP) in vitro.
目的：制备水飞蓟素固体分散缓释胶囊并考察其体外释放度。
OBJECTIVE to prepare sustained-release capsules Loaded with silymarin solid dispersions and to evaluate its releasing features in vitro.
体外释放度试验结果表明该胶乳分散体可用于缓释制剂的包衣。
The results showed that this colloidal aqueous dispersions could be used to prepare sustained release formulation.
结论：灰色数学模型可用于描述尼莫地平缓释片的体外释放度。
Conclusion: Gray mathematics model can used for the CARDS that describe the Captopril slow gives releases the slice releases the result outside.
结果表明羟丙甲纤维素与卡波姆对阻滞胶囊体外释放度影响较大。
The results showed that the amount of HPMC and Carbomer had remarkable effects on the in vitro release of capsules.
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.
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.
分别考察了上述因素对于控释片体外释放度的影响以及药物释放机制。
The factors that control the drug release character of the tablets were investigated. The drug release mechanism of the formulation was also studied.
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.
方法采用均匀设计优化包衣处方，对度米芬渗透泵片进行体外释放度试验。
Methods Coating prescription was optimized by uniform design and the drug release characteristic was tested 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).
制备膜控释盐酸二甲双胍缓释片并对其体外释放度的相关影响因素进行研究。
The membrane controlled-release coated tablets of metformin hydrochloride were prepared by coating method and the factors involved in the release rate of metformin hydrochloride in vitro were studied.
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.
并进行了灯盏花素壳聚糖纳米粒包封率、载药量、体外释放度、稳定性等试验研究。
The entrapment efficiency, drug load content, in vitro release and stability of Bre-CS-NP were studied.
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.
摘要：目的用醋酸钙梯度法制备阿魏酸脂质体，并考察其制备工艺及理化性质，进行体外释放度评价。
ABSTRACT: OBJECTIVE To evaluate the quality, physical and chemical properties and release of ferulic acid liposome via calcium acetate gradient.
摘要：目的用醋酸钙梯度法制备阿魏酸脂质体，并考察其制备工艺及理化性质，进行体外释放度评价。
ABSTRACT: OBJECTIVE To evaluate the quality, physical and chemical properties and release of ferulic acid liposome via calcium acetate gradient.
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