1) self-microemulsifying drug delivery system
自微乳化释药系统
1.
Optimization and evaluation of a new antischistosomal drug QH917 self-microemulsifying drug delivery system;
新型抗血吸虫药物QH917自微乳化释药系统的优化和评价
2.
Study on evaluation in vitro of release of itraconazole self-microemulsifying drug delivery system;
伊曲康唑自微乳化释药系统体外释放的评价方法
3.
Study on the absorption kinetics of vinpocetine self-microemulsifying drug delivery system in rat s intestine;
长春西汀自微乳化释药系统在大鼠小肠的吸收动力学
2) self-microemulsifying drug delivery system
自微乳释药系统
1.
Preparation and evaluation of self-microemulsifying drug delivery systems containing atorvastatin;
阿托伐他汀自微乳释药系统的制备和评价
2.
OBJECTIVE To prepare and evaluate self-microemulsifying drug delivery system(SMEDDS)of containing ginsenoside Rh2 for improving the in vitro drug dissolution and enhancing the in vivo drug absorption.
目的制备人参皂苷Rh2自微乳释药系统并进行评价,为人参皂苷Rh2口服制剂的开发提供参考。
3) self-emulsifying drug delivery system
自乳化释药系统
1.
Formulation optimization of lornoxicam self-emulsifying drug delivery system;
氯诺昔康自乳化释药系统处方优化的研究
2.
Formula optimization of simvastatin self-emulsifying drug delivery system and its pharmacokinetics in Beagle dogs
辛伐他汀自乳化释药系统处方优化及Beagle犬体内药代动力学
3.
Objective:To evaluate the enhancement of self-emulsifying drug delivery system(SEDDS)on the transport of indirubin across the intestinal mucosa of rat and the monolayer of Caco-2 cell,and investigate the pharmcokinetic process of indirubin SEDDS in beagle dogs.
目的:考察靛玉红自乳化释药系统的跨膜转运及其在犬体内的药动学过程。
5) oral self-emulsifying drug delivery system
口服自乳化释药系统
6) self-microemulsifying drug delivery system
自微乳化给药系统
1.
Preparation of the oral self-microemulsifying drug delivery system of GBE50
银杏酮酯口服自微乳化给药系统的制备
2.
OBJECTIVE To develop the formulation of self-microemulsifying drug delivery system for vinpocetine(VIN-SMEDDS).
目的研究长春西汀自微乳化给药系统(VIN-SMEDDS)的处方工艺。
3.
Self-microemulsifying drug delivery systems(SMEDDS), which are isoreopic mixture of oils, surfactants and/or co-surfactants, can be used for the design of formulation in order to improve the oral absorption of lipophilic drug compounds.
本文分别选择了十一酸睾酮(TU)和水飞蓟素(Silymarin)作为模型药物,制备了两种不同类型的自微乳化给药系统,分别进行了体内外的评价。
补充资料：自调自净自度
【自调自净自度】
（术语）同自调项。
（术语）同自调项。
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