Targeted delivery and controlled release of doxorubicin to cancer cells using modified single wall carbon nanotubes

被引:411
作者
Zhang, Xiaoke [1 ]
Meng, Lingjie [1 ]
Lu, Qinghua [1 ,2 ]
Fei, Zhaofu [3 ]
Dyson, Paul J. [3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Technol, Dept Polymer Sci & Engn, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[3] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
基金
中国国家自然科学基金;
关键词
Single wall carbon nanotubes (SWCNTs); Targeted drug delivery; Chitosan; Alginate sodium; Nanomedicine; NANOPARTICLES; TRANSPORTERS; BIODISTRIBUTION; SCAFFOLDS; VIABILITY;
D O I
10.1016/j.biomaterials.2009.07.025
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A targeted drug delivery system that is triggered by changes in pH based on single wall carbon nanotubes (SWCNTs), derivatized with carboxylate groups and coated with a polysaccharide material, can be loaded with the anticancer drug doxorubicin (DOX). The drug binds at physiological pH (pH 7.4) and is only released at a lower pH, for example, lysosomal pH and the pH characteristic of certain tumor environments. By manipulating the surface potentials of the modified nanotubes through modification of the polysaccharide coating, both the loading efficiency and release rate of the associated DOX can be controlled. Folic acid (FA), a targeting agent for many tumors, can be additionally tethered to the SWCNTs to selectively deliver DOX into the lysosomes of HeLa cells with much higher efficiency than free DOX. The DOX released from the modified nanotubes has been shown to damage nuclear DNA and inhibit the cell proliferation. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6041 / 6047
页数:7
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