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
1.
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。
2.
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。
3.
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。
4) in vitro dissolution
体外溶出度
1.
A study on in vitro dissolution of Ginkgo leaf tablets;
银杏叶片的体外溶出度研究
2.
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。
3.
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。
5) in vitro dissolution rate
体外溶出度
1.
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。
6) dissolution
[英][,dɪsə'lu:ʃn] [美]['dɪsə'luʃən]
体外溶出度
1.
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
2.
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。
3.
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。
补充资料：出体
【出体】
（术语）出诸法之体也。
（术语）出诸法之体也。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条