Multi-functionalized graphene oxide based anticancer drug-carrier with dual-targeting function and pH-sensitivity

被引:463
作者
Yang, Xiaoying [1 ]
Wang, Yinsong [1 ]
Huang, Xin [2 ]
Ma, Yanfeng [3 ,4 ]
Huang, Yi [3 ,4 ]
Yang, Rongcun [2 ]
Duan, Hongquan [1 ]
Chen, Yongsheng [3 ,4 ]
机构
[1] Tianjin Med Univ, Sch Pharmaceut Sci, Basic Med Res Ctr, Tianjin 300070, Peoples R China
[2] Nankai Univ, Dept Immunol, Coll Med, Key Lab Bioact Mat,Minist Educ, Tianjin 300071, Peoples R China
[3] Nankai Univ, Coll Chem, Ctr Nanoscale Sci & Technol, Tianjin 300071, Peoples R China
[4] Nankai Univ, Coll Chem, Key Lab Funct Polymer Mat, Inst Polymer Chem, Tianjin 300071, Peoples R China
关键词
COPOLYMER MICELLES; CARBON NANOTUBES; DELIVERY SYSTEMS; CANCER-CELLS; TRANSPORTERS; AGENTS; FILMS;
D O I
10.1039/c0jm02494e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A dual-targeting drug delivery and pH-sensitive controlled release system based on multi-functionalized graphene oxide (GO) was established in order to enhance the effect of targeted drug delivery and realize intelligently controlled release. A superparamagnetic GO-Fe3O4 nanohybrid was firstly prepared via a simple and effective chemical precipitation method. Then folic acid, a targeting agent toward some tumor cells, was conjugated onto Fe3O4 nanoparticles via the chemical linkage with amino groups of the 3-aminopropyl triethoxysilane (APS) modified superparamagnetic GO-Fe3O4 nanohybrid, to give the multi-functionalized GO. Doxorubicin hydrochloride (Dox) as an anti-tumor drug model was loaded onto the surface of this multi-functionalized GO via pi-pi stacking. The drug loading capacity of this multi-functionalized GO is as high as 0.387 mg mg(-1) and the drug release depends strongly on pH values. Cell uptake studies were carried out using fluorescein isothiocyanate labeled or Dox loaded multi-functionalized GO to evaluate their targeted delivery property and toxicity to tumor cells. The results show that this multi-functionalized GO has potential applications for targeted delivery and the controlled release of anticancer drugs.
引用
收藏
页码:3448 / 3454
页数:7
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