期刊文献+

一种全新合成的抗抑郁药物的自微乳化载药系统(SMEDDS)理化性质和体外释药行为研究 被引量:3

Self-microemulsifying drug delivery system(SMEDDS) for a novel medicative compound against depression: physicochemical property and in vitro release
下载PDF
导出
摘要 目的研究一种全新合成的抗抑郁药物AJS的自微乳化制剂(AJS-SMEDDS)的理化性质和体外释药行为。方法考察AJS-SMEDDS制剂的黏度、zeta电位和粒度,研究其流变学性质及电学性质;采用总体液平衡反向透析法测定其体外释药性能;并考察了其稳定性。结果 AJS-SMEDDS制剂为塑性流体,在分散介质中所形成的乳滴zeta电位为-2.76 m V,粒径为(26.08±1.68)nm,制剂质量稳定,低温不影响其性能。结论 AJSSMEDDS制剂质量稳定,适合工业生产。 Objective To study the physicochemical properties and in vitro release of a self-microemulsifying drug delivery system( SMEDDS)of AJS,the code name of an untitled novel medicative compound. Methods To study the rheo-logical properties and electrical properties of AJS-SMEDDS by examining its viscosity,zeta potential and particle size. The in vitro release of AJS-SMEDDS was examined by the bulk-equilibrium reverse dialysis bag technique. The stability of AJS-SMEDDS was also examined. Results AJS-SMEDDS was a plastic fluid with a zeta potential of -2. 76 mV and a particle size of(26. 08±1. 68)nm. The quality of AJS-SMEDDS was stable during storing period in room temperature as well as low temperature. Conclusion AJS-SMEDDS was suitable for industrial production with a stable quality.
出处 《药学研究》 CAS 2015年第4期215-218,共4页 Journal of Pharmaceutical Research
基金 国家"十二五""重大新药创制"科技重大专项(No.2013zx09402202) 天津市科技支撑计划重点项目(No.12ZCZDSY01200)
关键词 自微乳化载药系统 粒径 流体 稳定性 释放 Self-microemulsifying drug delivery system( SMEDDS) Particle size Fluid Stability Drug release
  • 相关文献

参考文献7

  • 1Wu W, Wang Y, Que L. Enhanced bioavailability of sily- marin by self- microemulsifying drug delivery system [ J]. Eur J Pharm Biopharm,2006,63 (3) :288 - 294.
  • 2Balakrishnan P, Lee BJ, Oh DH, et al. Enhanced oral bio- availability of Coenzyme Q10 by self - emulsifying drug de- livery systems [ J ]. Int J Pharm,2009,374 ( 1 - 2) :66 - 72.
  • 3Amri A, Le Clanche S, Thfirond P, et al. Resveratrol self- emulsifying system increases the uptake by endothelial cells and improves protection against oxidative stress - mediated death [ J ]. Eur J Pharm Biopharm, 2014, 86 (3) :418 -426.
  • 4施庆珊,王计伟,欧阳友生,等.非牛顿流体粘度测定方法研究进展[J].发酵科技通讯,2011,40(2) :42-45.
  • 5陈柳钦,崔名全,尹蓉莉,朱双燕,张立,李开.脱水穿心莲内酯自乳化制剂的制备及质量评价[J].中国实验方剂学杂志,2013,19(11):28-31. 被引量:4
  • 6王慧云,崔亚男,张春燕.影响胶体粒子zeta电位的因素[J].中国医药导报,2010,7(20):28-30. 被引量:24
  • 7刘华,李三鸣,袁悦,郎轶咏,刘凯.酮洛芬自乳化制剂的释药动力学研究[J].沈阳药科大学学报,2005,22(2):91-95. 被引量:11

二级参考文献31

  • 1钱一鑫,唐景玲,孙进,张天虹,何仲贵.口服自乳化释药系统及其在中药制剂中的应用[J].中草药,2006,37(10):1441-1446. 被引量:17
  • 2胡英,陈海靓,梁文权.槲皮素自乳化释药系统的制备和质量评价[J].中国中药杂志,2007,32(9):805-807. 被引量:19
  • 3Henry DC The catophoresis of suspended particles,the surface conductivity effect,trans[J].Faraday Sci,1948,(44):1021-1026.
  • 4Russell AS,Scales PJ,Underwood SM.An electrophoretic investigation of the relaxation term in electrokinetic theory[J].Langmuir,1995,(11):1112-1115.
  • 5Dukhin SS,Derjnguin BV.Electrokinetic phenomena in surface and colloid science[M].New York:Wiley,1974.
  • 6Midmore BB,Pratt GV,Herrington TM.Evidence for the validity of electrokinetic theory in the thin double layer region[J].Colloid and Interface Science,1996,(184):170-174.
  • 7Roy MT,Gallardo M,Estelrich J.Influence of size on electrokinetic behavior of phosphatidylserine and phosphatidylethanolamine lipid vesicles[J].Colloid and Interface Science,1998,(206):512-517.
  • 8Gholabzouri OE,Cabrerizo MA,Alvarez RH.The surface charge density influence on the electrokinetic properties of model colloids; solvent composition effect[J].Colloid and Interface Science,1999,(214):243-250.
  • 9Gholabzouri OE,Cabrerizo MA,Alvares RH.Electrokinetic phenomena[M].Austria:Salzburg,1998.
  • 10McNeil-Watson F,Tscharnuter W,Miller J.A new instrument for the measurement of very small electrophoreric mobilities using phase analysis light scattering[J].Colloids and Surfaces,1998,140(1):53-57.

共引文献38

同被引文献35

引证文献3

二级引证文献19

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部