期刊文献+

CS-ISPH-TPP亚微米颗粒的粒径与表面电位影响因素研究

Study on the influence factors of particle size and zeta potential of CS-ISPH-TPP submicron particles
下载PDF
导出
摘要 以带正电的几丁聚醣(CS)与带负电的三聚磷酸钠(TPP)通过离子交联作用包覆分离大豆蛋白质水解物(ISPH)制成CS—ISPH—TPP亚微米颗粒,利用动态光散射法分析ISPH浓度、CS分子量及CS/TPP质量比对亚微米颗粒的粒径与表面电位的影响。结果表明,CS-ISPH-TPP亚微米颗粒的粒径随ISPH添加浓度的增加而增大,而表面电位则无明显变化。CS—TPP与CS-ISPH—TPP亚微米颗粒的粒径会随CS分子量的增加而增大,且包覆ISPH颗粒的粒径均大于未包覆的颗粒,而表面电位则介于41.9~44.2mV之间。CS/TPP质量比由6:1减至4:1时,颗粒粒径会随之增加,而由4:1减至2:1时,粒径则变小;CS/TPP质量比由6:1减至3:1时,颗粒表面均带有高度的正电荷,继续减至2:1时,表面电位会出现骤降的情形。 CS-ISPH-TPP nanoparticles were prepared by isolated soy protein hydrolysate being coated through ionic crosslinking between chitosan hydrolysate(CS) with negative charge and sodium tripolyphosphate (TPP) with positive charge. The effects of ISPH concentration, chitosan molecular weight and CS/TPP mass ratio on the size and zeta potential of these nanoparticles were investigated by dynamic light scattering method. The results showed that, the size of CS-ISPH-TPP nanoparticles increased with ISPH concentration increasing and there was no obvious change in zeta potential. The size of CS-TPP and CS-ISPH-TPP nanoparticles increased with chitosan molecular weight increasing and zeta potential lied during 41.9 -44.2 mV. The size of CS-TPP and CS-ISPH-TPP nanoparticles increased for CS/TPP mass ratio decreasing from 6 : 1 to 4 : 1 and decreased for CS/TPP mass ratio decreasing from 4 : 1 to 2 : 1. The surface of CS-TPP and CS-ISPH-TPP nanoparticles possessed a high degree of positive charge for CS/TPP mass ratio decreasing from 6 : 1 to 4 : 1 and the zeta potential decreased rapidly for CS/TPP mass ratio decreasing from 4 : 1 to 2 : 1.
作者 娄本浊
出处 《陕西理工学院学报(自然科学版)》 2015年第5期73-78,共6页 Journal of Shananxi University of Technology:Natural Science Edition
基金 国家自然科学基金资助项目(41105107) 陕西省自然科学基础研究计划项目(2012JM5014)
关键词 动态光散射 CS—ISPH-TPP 纳米颗粒 粒径 表面电位 dynamic light scattering CS-ISPH-TPP submicron particle particle size zeta potential
  • 相关文献

参考文献10

  • 1KO J A, PARK H J, HWANG S J, et al. Preparation and characterization of chitosan microparticles intended for controlled drug delivery[ J ]. International Journal of Pharmaceutics ,2002,249 (1/2) : 165-174.
  • 2XU Y, DU Y. Effect of molecular structure of chitosan on protein delivery properties of chitosan nanoparticles [ J ]. Interna- tional Journal of Pharmaceutics,2003,250 ( 1 ) : 215-226.
  • 3GAN Q, WANG T, COHRANE C, et al. Modulation of surface charge, particle size and morphological properties of chi- tosan-TPP nanoparticles intended for gene delivery[ J ]. Colloids and Surfaces B. Biointerfaces, 2005,44 (2/3) :65-73.
  • 4WU Y,YANG W,WANG C ,et al. Chitosan nanoparticles as a novel delivery system for ammonium glycyrrhizinate[ J]. In- ternational Journal of Pharmaceutic s, 2005,295 ( 1/2 ) : 235-245.
  • 5GREHA A, SEIJO B, REMUNAN-LOPEZ C. Microencapsulated chitosan nanoparticles for lung protein delivery [ J ]. Euro- pean Journal of Pharmaceutical Sciences, 2005,25 ( 4/5 ) : 427-437.
  • 6GAN Q, WANG T. Chitosan nanoparticle as protein deliverycarrier-systematic examination of fabrication conditions for effi- cient loading and release[ J]. Colloids and Surfaces B : Biointerfaces ,2007,59 (1) :24-34.
  • 7JANG K I, LEE H G. Stability of chitosan nanoparticles for L-Ascorbic acid during heat treatment in aqueous solution [ J ]. Food Chemistry,2008,56(6) :1936-1941.
  • 8LIU Hui, GAO Chang-you. Preparation and properties of ionically cross-linked chitosan nanoparticles [ J ]. Polymers for Ad- vanced Technologies ,2009,20( 8 ) :613-619.
  • 9娄本浊.包覆染料木黄酮纳米胶囊的动态光散射研究[J].激光与光电子学进展,2013,50(10):147-151. 被引量:5
  • 10XIA Hui, XIAO Yuan-yuan, HUANG Hao, et al. Particle sizing of colloidal suspensions by low-coherence fiber optic dy- namic light scattering[ J ]. Journal of Colloid and Interface Science ,2012,367 (1) :527-530.

二级参考文献12

共引文献4

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