Enhancement of radiation cytotoxicity in breast-cancer cells by localized attachment of gold nanoparticles

被引:281
作者
Kong, Tao [5 ]
Zeng, Jie [5 ]
Wang, Xiaoping [5 ]
Yang, Xiaoyan [1 ]
Yang, Jing [1 ]
McQuarrie, Steve [3 ,4 ]
McEwan, Alexander [3 ,4 ]
Roa, Wilson [3 ,4 ]
Chen, Jie [1 ]
Xing, James Z. [2 ]
机构
[1] Univ Alberta, Dept Elect & Comp Engn, Edmonton, AB, Canada
[2] Univ Alberta, Dept Lab Med & Pathol, Edmonton, AB, Canada
[3] Univ Alberta, Cross Canc Inst, Edmonton, AB, Canada
[4] Univ Alberta, Dept Oncol, Edmonton, AB, Canada
[5] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei, Peoples R China
关键词
breast cancer; cytotoxicity; drug delivery; irradiation; nanoparticles;
D O I
10.1002/smll.200700794
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gold nanoparticles (GNPs) and modified GNPs having two kinds of functional molecules, cysteamine (AET) and thioglucose (Glu), are synthesized. Cell uptake and radiation cytotoxicity enhancement in a breast-cancer cell line (MCF-7) versus a nonmalignant breast-cell line (MCF-10A) are studied. Transmission electron microscopy (TEM) results show that cancer cells take up functional Glu-GNPs significantly more than naked GNPs. The TEM results also indicate that AET-capped GNPs are mostly bound to the MCF-7 cell membrane, while Glu-GNPs enter the cells and are distributed in the cytoplasm. After MCF-7 cell uptake of Glu-GNPs, or binding of AET-GNPs, the in vitro cytotoxicity effects are observed at 24, 48, and 72 hours. The results show that these functional GNPs have little or no toxicity to these cells. To validate the enhanced killing effect on cancer cells, various forms of radiation are applied such as 200 kVp X-rays and gamma-rays, to the cells, both with and without functional GNPs. By comparison with irradiation alone, the results show that GNPs significantly enhance cancer killing.
引用
收藏
页码:1537 / 1543
页数:7
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