Objective: To prepare flurbiprofen coated pellets and evaluate its release characteristics in vitro.
目的：制备氟比洛芬包衣小丸，评价其体外释药特性。
OBJECTIVE To develop naproxen enteric-coated pellets and evaluate its release characteristics in vitro.
目的：研制萘普生肠溶微丸，评价其体外释药特性。
AIM To develop a novel pulsatile drug delivery system of which the lag time is cont rolled by an erodible plug (EP) and evaluate its release characteristics in vitro.
目的制备一种由溶蚀塞控制时滞的新型脉冲给药系统并对其体外释药行为进行评价。
Objective to study the release characteristics of fluorouracil-loaded carboxymethyl chitosan microspheres (Fu-CMCS-MS) in vitro.
目的探讨对以羧甲基壳聚糖为载体的氟尿嘧啶微球体外释药特性的影响因素。
Objective To determine the content uniformity and controlled release characteristics of transdermal nitroglycerin in vitro.
目的测定硝酸甘油贴膜的含量均匀度和体外释放度。
Objective: To investigate in vitro release characteristics of collagen double layer minipellet of erythropoietin(EPO).
前言： 目的：对红细胞生成素胶原蛋白双层微条的体外释放特性进行研究。
OBJECTIVE: to prepare aspirin gastric floating capsule and to study its in vitro drug-release characteristics.
目的：制备小剂量阿司匹林胃漂浮胶囊并研究其体外释药特征。
OBJECTIVE:To investigate the characteristics of drug release and the factors affecting the in vitro dissolubility of diclofenac potassium double-layer tablets(DPD).
目的：考察双氯酚酸钾双层片的体外释放特征及其影响因素。
To prepare PLGA microspheres of cobra venom cytotoxin and study its characterization and characteristics of in vitro release; 3.
制备眼镜蛇毒细胞毒素plga微球，研究其表征及体外释药性质；3。
The invention discloses in vitro drug release characteristics and preparation method thereof.
本发明公开了该缓释制剂的体外释药特性及制备方法。
Objective to study the release characteristics of fluorouracil-loaded carboxymethyl chitosan microspheres (Fu-CMCS-MS) in vitro.
目的探讨羧甲基壳聚糖包药微球体的制备及体外释药特性。
The in vitro release characteristics investigated fitted to first order pharmacokinetic model.
体外释药速率符合一级动力学模型。
Objective: To evaluate the electrochemical corrosion characteristics and elemental release of laser-welded dissimilar alloy in dentistry: Co-Cr and Ni-Cr alloy in vitro.
目的：研究激光焊接钴铬-镍铬合金的体外电化学行为及离子释出情况。
The release characteristics and anti-tumor activities of CCNU-TSL in vitro were investigated.
并考察脂质体的体外释药特性和体外抗肿瘤活性。
To prepare microsphere containing Azithromycin(AZM) with polylactic acid, and investigate the characteristics of AZM microsphere (AZMMS)in vitro release.
以聚乳酸为载体材料制备阿奇霉素微球（AZMMS）并考察其体外释药特性。
ConclusionRuyijinhuangsan film prepared with Chitosan-graft-poly (Methyl Methacrylate) is more flexible and has better characteristics of sustained-release in vitro than former film.
结论以壳聚糖接枝甲基丙烯酸甲酯共聚物为成膜材料制备如意金黄散膜剂柔性更好，大黄酸体外缓释效果更明显。
ConclusionRuyijinhuangsan film prepared with Chitosan-graft-poly (Methyl Methacrylate) is more flexible and has better characteristics of sustained-release in vitro than former film.
结论以壳聚糖接枝甲基丙烯酸甲酯共聚物为成膜材料制备如意金黄散膜剂柔性更好，大黄酸体外缓释效果更明显。
应用推荐