Department of Pharmaceutics, College of Pharmacy, Shandong University, Jinan 250012, China.
Department of Pharmaceutics, College of Pharmacy, Shandong University, Jinan 250012, China.
Colloids Surf B Biointerfaces. 2016 Oct 1;146:235-44. doi: 10.1016/j.colsurfb.2016.06.019. Epub 2016 Jun 14.
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.
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。