Intercellular pH-responsive histidine modified dextran-g-cholesterol micelle for anticancer drug delivery

被引:33
作者
Yao, Xuemei [1 ]
Chen, Li [1 ]
Chen, Xiaofei [1 ]
He, Chaoliang [2 ]
Zheng, Hui [2 ]
Chen, Xuesi [2 ]
机构
[1] NE Normal Univ, Dept Chem, Changchun 130022, Peoples R China
[2] Changchun Inst Appl Chem, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
Dextran-g-cholesterol; Histidine; pH-responsive; Micelle; Drug delivery; NANOPARTICLES; COPOLYMER; DOXORUBICIN; PARTICLES; RELEASE; SIRNA;
D O I
10.1016/j.colsurfb.2014.05.032
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Herein, the micelles based on histidine modified dextran-g-cholesterol (HDC) were successfully prepared which exhibited excellent pH-responsive behavior in acidic aqueous solution (pH < 6, within the range of malignant cellular endosome). Taking advantage of this pH-sensitivity in acidic conditions, doxorubicin (DOX), a model anticancer drug, was effectively loaded into the micelles via hydrophobic interactions. The DOX release from all DOX-loaded micelles was accelerated in acid conditions mimicking the endosomal/lysosomal compartments. The enhanced intracellular DOX release was also observed in MCF-7 cells. DOX-loaded pH-sensitive micelles showed higher cellular proliferation inhibition toward MCF-7 cells than that of pH-insensitive micelles. These features suggested that the micelles could efficiently load and deliver DOX into tumor cells, which can enhance the inhibition of cellular proliferation in vitro, providing a powerful mean for delivering and releasing cargoes at the tumor sites. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:36 / 43
页数:8
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