基本释义:

聚体溶度

网络释义

1)solubility of polymers,聚体溶度

2)water-soluble polymers,水溶性聚体

3)dissolution in vitro,体外溶出度

4)in vitro dissolution,体外溶出度

5)in vitro dissolution rate,体外溶出度

6)dissolution,体外溶出度

用法和例句

The test of dissolution in vitro was performed by RC-3D dissolution instrument with roling basket for 12 pilles BBSRC.

实验结果是(1)体外溶出度按取样时间点为序(h)是05、1、2、4、6、8、10、12、14、16、18、20。

Coating formula of Nimesulide sustained release pellet capsules and the dissolution in vitro were tested using orthogonal design methods.

制备尼美舒利缓释微丸胶囊及测定体外溶出度。

And the physic-chemical characters and dissolution in vitro of ITZ-SEDDS were also determined.

并对ITZ-SEDDS的理化性质和体外溶出度进行了测定。

A study on in vitro dissolution of Ginkgo leaf tablets;

银杏叶片的体外溶出度研究

The micromeritic properties and in vitro dissolution of the pellets were determined.

方法利用挤出滚圆法制备微丸,采用L9(34)正交设计试验优化了工艺条件,并考察了微丸的粉体学性质及体外溶出度。

The micromeritic properties, reception percentage and in vitro dissolution of pellets with different spheroniser load were determined.

方法用新型的挤出滚圆造粒机制备杞芪微丸;采用L_9(3~4)正交设计实验优化制剂工艺条件;考察了不同处方微丸的粉体学性质、收率和体外溶出度。

OBJECTIVE To observe the in vitro dissolution rate of tetrandrine in nickel-titanium alloy stent.

目的　考察载药带膜镍钛金属支架中粉防己碱体外溶出度。

Study on the dissolution rate of tramadol hydrochloride by UV-spectrophotometry;

盐酸曲马多口服制剂体外溶出度考察

An UV method for determination of dissolution of loxoprofen sodium tablets was established according to ChP dissolution methodⅡ.

参照中国药典2005年版溶出度试验第二法,建立了UV法测定洛索洛芬钠片体外溶出度的试验方法,并用HPLC法测定洛索洛芬钠片的人体药物动力学,进行了体内外相关性的评价。

Objective: To improve the dissolution rate of nifedipin tablets in vitro.

方法 :分别考察药物粒度、稀释剂、崩解剂对体外溶出度的影响 ,比较溶出特性曲线筛选处方。

Comparison of in Vitro Dissolution of Omeprazole Enteric-coated Capsules from Seven Different Pharmaceutical Factories

不同厂家奥美拉唑肠溶胶囊的体外溶出度比较

Comparison of dissolution of sparfloxacin tablets in vitro from different pharmaceutical factories

不同厂家司帕沙星片体外溶出度比较

Preparation of Usolic Acid Solid Dispersion Systems and Study on Their Dissolution in Vitro;

乌索酸固体分散体的制备及其体外溶出度研究

Study on the dissolution of tamoxifen citrate tablets of different companies in vitro

5个企业枸橼酸他莫昔芬片的体外溶出度考察

Determination and Significance on the Dissolution Rate in Vitro of Co.Sophora Alopecuroides Suppository

复方苦豆子栓剂体外溶出度的测定及意义

Study on the dissolution in vitro of isofraxidin in Xuanshenliangxue Dispersible Tablets

玄参凉血分散片中异嗪皮啶的体外溶出度研究

Study on the dissolution of levofloxacin tablets from different manufacturers in vitro

不同厂家左氧氟沙星片体外溶出度考察

Dissolution in Vitro of Salbutamol Sulfate Tablets from Different Manufacturers

不同厂家硫酸沙丁胺醇片体外溶出度比较

Comparison of Dissolution Rates of Cefetamet Pivoxil Hydrochloride Tablets and Its Capsules from 4 Manufacturers in vitro

盐酸头孢他美酯片剂与胶囊剂体外溶出度比较

Preparation and in vitro dissolution of Yufengningxin dispersible tablets

愈风宁心分散片的制备及体外溶出度的研究

Comparison of Dissolution of Phenytoin Sodium Tablets from Different Pharmaceutical Companies in Vitro

不同厂家苯妥英钠片的体外溶出度比较

Preparation and Dissolution of Sulfamethoxazole Solid Dispersion;

磺胺甲噁唑固体分散体的制备及体外溶出度研究

Preliminary study of dissolution rate method in vitro of Chinese medicine solid preparations based on bio-thermal activity

基于生物热活性评价中药固体制剂体外溶出度方法学研究

OBJECTIVEA method for the determination of dissolution of fenofibrate chewable tablets in vitro was established.

目的:建立非诺贝特咀嚼片体外溶出度试验测定方法。

Through the FOCSDT new equation group solution have monitored dissolution of compound chlorzoxazone tablets.

通过FOCSDT联立方程组新解法监测了复方氯唑沙宗片体外溶出度。

Preparation and Dissolution Determination of Inclusion Compound Capsule of Baicalin with β-CD

黄芩苷-β-CD包合物胶囊的制备和体外溶出度测定

Preparation of Isoniazid-contained Drug Layer Alloy Stent and Its Dissolution in Vitro

含异烟肼药膜型金属支架的制备及体外溶出度试验

Preparation of Rapid-release Nifedipine Tablet by Fluidized Bed Granulation and Study on Its in Vitro Dissolution

流化床制粒法制备速释硝苯地平片及其体外溶出度研究