Switching off the interactions between graphene oxide and doxorubicin using vitamin C: combining simplicity and efficiency in drug delivery

被引:26
作者
Liu, Zhen [1 ]
Liu, Jingquan [2 ]
Wang, Tao [3 ,4 ]
Li, Qiong [4 ]
Francis, Paul S. [1 ]
Barrow, Colin J. [1 ]
Duan, Wei [4 ]
Yang, Wenrong [1 ]
机构
[1] Deakin Univ, Sch Life & Environm Sci, Ctr Chem & Biotechnol, Geelong, Vic 3216, Australia
[2] Qingdao Univ, Coll Chem Sci & Engn, Lab Fiber Mat & Modern Text, Growing Base State Key Lab, Qingdao, Peoples R China
[3] Zhengzhou Univ, Sch Nursing, Zhengzhou, Henan, Peoples R China
[4] Deakin Univ, Fac Hlth, Sch Med, Geelong, Vic 3216, Australia
基金
澳大利亚研究理事会;
关键词
CONTROLLED-RELEASE; TARGETED DELIVERY; CARBON NANOTUBES; CANCER-CELLS; NANOPARTICLES; THERAPY; NANOMATERIALS; NANOCARRIERS; COMPOSITES; GRAPHITE;
D O I
10.1039/c7tb03063k
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Well-controlled, low-toxicity and highly efficient delivery systems for anticancer drugs are a key challenge for the development of a new class of nanocarrier systems for cancer chemotherapy. Graphene oxide (GO) has been developed to be a nanocarrier of anti-cancer drugs due to its large surface area and biocompatibility; however, understanding of the interface chemistry is very limited. In this work, we report efficient loading and controlled release of doxorubicin (DOX) using the tunable surface of GO. A deep understanding of the surface chemistry between GO and DOX is achieved using spectroscopies and atomic force microscopy. Hydrogen bonding and pi-pi stacking are confirmed to be the non-covalent interactions between the drugs and the carriers. As a result, improvement of DOX delivery from the GO surface can be achieved using vitamin C.
引用
收藏
页码:1251 / 1259
页数:9
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