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基于硫酸软骨素-脱氧胆酸缀合物的自组装纳米粒子用于多西紫杉醇递送:脱氧胆酸取代度的影响。

Self-assembled nanoparticles based on chondroitin sulfate-deoxycholic acid conjugates for docetaxel delivery: Effect of degree of substitution of deoxycholic acid.

机构信息

Department of Pharmaceutics, College of Pharmacy, Shandong University, Jinan 250012, China.

Department of Pharmaceutics, College of Pharmacy, Shandong University, Jinan 250012, China.

出版信息

Colloids Surf B Biointerfaces. 2016 Oct 1;146:235-44. doi: 10.1016/j.colsurfb.2016.06.019. Epub 2016 Jun 14.

Abstract

Hydrophobically-modified polymers based on chondroitin sulfate with different degree of substitution (DS) of deoxycholic acid (DOCA) were developed for docetaxel delivery. Chondroitin sulfate-deoxycholic acid (CSAD) bioconjugates were synthesized via the linker of adipic dihydrazide by amide bond. They were characterized with spherical shape, mean diameter of around 165.2nm and negative zeta potential (-14.87 to -20.53mV). An increase of DOCA DS reduced size of nanoparticles, while increasing drug loading efficiency. Drug release in vitro showed a triphasic sustained pattern and higher accumulative drug release percentage was observed with increased DS of DOCA on polymer. Self-assemblies with higher DS also had enhanced internalization of nanoparticles and stronger cytotoxicity at the cellular level. The self-assemble nanoparticles demonstrate to be excellent targeting drug delivery systems and the desired therapeutics can be achieved via the alteration of DS.

摘要

基于硫酸软骨素的具有不同去氧胆酸取代度(DS)的疏水改性聚合物被开发用于多西他赛的递送。硫酸软骨素-去氧胆酸(CSAD)通过酰肼键的连接体通过酰胺键合成。它们具有球形,平均直径约为 165.2nm 和负 ζ 电位(-14.87 至-20.53mV)。去氧胆酸 DS 的增加会减小纳米颗粒的尺寸,而增加药物载药效率。体外药物释放呈现出三相持续释放模式,并且随着聚合物上 DOCA DS 的增加,观察到更高的累积药物释放百分比。具有更高 DS 的自组装还增强了纳米颗粒的内化作用,并在细胞水平上表现出更强的细胞毒性。自组装纳米颗粒表现出优异的靶向药物递送系统,并且可以通过改变 DS 来实现所需的治疗效果。

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