Size-dependent genotoxicity of graphene nanoplatelets in human stem cells

被引:734
作者
Akhavan, Omid [1 ,2 ]
Ghaderi, Elham [1 ]
Akhavan, Alireza [1 ]
机构
[1] Sharif Univ Technol, Dept Phys, Tehran, Iran
[2] Sharif Univ Technol, Inst Nanosci & Nanotechnol, Tehran, Iran
关键词
Reduced graphene Oxide; Nanoscale lateral dimension; Size effect; Cytotoxicity; Genotoxicity; Stem cells; WALL CARBON NANOTUBES; OXIDE; CYTOTOXICITY; REDUCTION; ANTIOXIDANT; ENVIRONMENT; NANOSHEETS; TOXICITY; BACTERIA; DELIVERY;
D O I
10.1016/j.biomaterials.2012.07.040
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Reduced graphene oxide nanoplatelets (rGONPs) were synthesized by sonication of covalently PEGylated GO sheets followed by a chemical reduction using hydrazine and bovine serum albumin. Human mesenchymal stem cells (hMSCs), as a fundamental factor in tissue engineering, were isolated from umbilical cord blood (as a recently proposed source for extracting fresh hMSCs) to investigate, for the first time, the size-dependent cyto- and geno-toxic effects of the rGONPs on the cells. The cell viability test showed significant cell destructions by 1.0 mu g/mL rGONPs with average lateral dimensions (ALDs) of 11 +/- 4 nm, while the rGO sheets with ALDs of 3.8 +/- 0.4 mu m could exhibit a significant cytotoxic effect only at highconcentration of 100 mu g/mL after 1 h exposure time. Although oxidative stress and cell wall membrane damage were determined as the main mechanism involved in the cytotoxicity of the rGO sheets, neither of them could completely describe the cell destructions induced by the rGONPs, especially at the concentrations <= 1.0 mu g/mL. In fact, the rGONPs showed genotoxic effects on the stem cells through DNA fragmentations and chromosomal aberrations, even at low concentration of 0.1 mu g/mL. Our results present essential knowledge for more efficient and innocuous applications of graphene sheets and particularly nanoplatelets in upcoming nanotechnology-based tissue engineering as, e.g., drug transporter and scaffolds. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8017 / 8025
页数:9
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