Sensitive detection of superoxide anion released from living cells using silver nanoparticles and functionalized multiwalled carbon nanotube composite

被引:29
|
作者
Liu, Xinhe [1 ]
Liu, Xiuhui [1 ]
Wei, Hongwei [1 ]
Song, Guangjie [1 ]
Guo, Huixia [1 ]
Lu, Xiaoquan [1 ]
机构
[1] Northwest Normal Univ, Coll Chem & Chem Engn, Key Lab Bioelectrochem & Environm Anal Gans Prov, Lanzhou 730070, Gansu, Peoples R China
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2017年 / 252卷
基金
中国国家自然科学基金;
关键词
Superoxide anion; Non-enzymatic sensor; Functionalized carbon nanotubes; Silver nanoparticles; Living cell; HYDROGEN-PEROXIDE; MODIFIED ELECTRODE; REACTIVE OXYGEN; IN-VIVO; AG NANOPARTICLES; BIOSENSOR; SENSOR; DISPERSION; DISMUTASE; RADICALS;
D O I
10.1016/j.snb.2017.06.027
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Considering the crucial roles of superoxide anion (O-2(center dot-)) in pathological conditions, it is of great urgency to establish a reliable approach for real-time determination of O-2(center dot-). Herein, a sensitive non-enzymatic sensor was constructed based on silver nanoparticles (AgNPs) and sodium dodecyl sulfate functionalized carbon nanotubes (SDS-MWCNTs) composites to measure the release of O-2(center dot-) from living cells. As an analytical and sensing platform, the AgNPs/SDS-MWCNTs modified glassy carbon electrode exhibited excellent electrochemical performance toward O-2(center dot-) with a determination limit as low as 0.0897 nM and wide linear range of 6 orders of magnitude, which was superior to other O-2(center dot-) electrochemical sensors. The excellent performance was attributed to the SDS-MWCNTs composites being used as effective load matrix for the deposition of AgNPs. Importantly, this novel non -enzymatic sensor could be applied to determination of Of-released from living cells, and the amount of flux of O-2(center dot-) increased accordingly with the improving of the concentration of AA, which has the possibility of application in clinical diagnostics to assess oxidative stress of living cells. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:503 / 510
页数:8
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