Spongy graphene electrode in electrochemical detection of leukemia at single-cell levels

被引:101
作者
Akhavan, Omid [1 ,2 ]
Ghaderi, Elham [3 ]
Rahighi, Reza [1 ]
Abdolahad, Mohammad [4 ]
机构
[1] Sharif Univ Technol, Dept Phys, Tehran, Iran
[2] Sharif Univ Technol, Inst Nanosci & Nanotechnol, Tehran, Iran
[3] Div Adv Mat, Nanobiotechnol Res Lab, Tehran, Iran
[4] Univ Tehran, Nanoelect & Thin Film Lab, Nanoelect Ctr Excellence, Sch Elect & Comp Engn, Tehran, Iran
基金
美国国家科学基金会;
关键词
CANCER-CELLS; OXIDE; IMMOBILIZATION; MONOLAYER; OXIDATION; LAYER; DIFFERENTIATION; GENOTOXICITY; SENSITIVITY; GUANINE;
D O I
10.1016/j.carbon.2014.08.058
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
Mg2+-charged spongy graphene electrodes (SGEs) were fabricated by using electrophoretic deposition of chemically exfoliated graphene oxide sheets on graphite rods. The SGEs were able to present two distinguishable signals (originated from electrochemical oxidation of guanine) in differential pulse voltammetry (DPV) of leukemia and normal blood cells, in contrast to glassy carbon electrodes giving only one overlapped peak. Hence, the SGEs were applied in fast (60 min) and ultra sensitive detection of leukemia (single abnormal cells in similar to 10(9) normal cells) in a blood serum. The sensitivity obtained by the SGEs was three orders of magnitude better than that of the best available and current technologies (e.g., specific mutations by polymerase chain reaction with detection limit of one abnormal cell in similar to 10(6) normal cells) which not only are expensive, but also require several days for incubation. Significant variations in DPV signals of the SGEs after the first electrochemical cycle indicated that the best performance of the SGEs can be achieved only at the first cycle. The linear dynamic detection behavior of the SGEs was investigated in wide concentration range of 1.0 x 10(5)-0.1 cell/mL. The lower detection limit was estimated similar to 0.02 celVmL, based on the current resolution obtained by the SGEs. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:654 / 663
页数:10
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