Ultrasensitive photoelectrochemical immunoassay through tag induced exciton trapping

被引:29
作者
Wen, Guangming [1 ,2 ]
Ju, Huangxian [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
[2] Shanxi Univ, Sch Chem & Chem Engn, Taiyuan 030006, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Photoelectrochemistry; Immunoassay; Quantum dots; Exciton trapping; alpha-Fetoprotein; ALPHA-FETOPROTEIN; QUANTUM DOTS; FLUORESCENT NANOPARTICLES; GOLD NANOPARTICLES; VISIBLE-LIGHT; IMMUNOSENSOR; FLUOROIMMUNOASSAY; AMPLIFICATION; COPPER(II); ANTIGEN;
D O I
10.1016/j.talanta.2014.11.041
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The development of photoelectrochemical (PEC) sensors with novel principles is of significance in realizing sensitive and low-cost detection. This work uses CuO NPs labeled antibody to construct a simple and sensitive sandwich-type immunobiosensor for the detection of protein. The detection signal is produced by dissolving the CuO NPs to release copper ions, which are then added on a quantum dots (QDs) modified F-doped tin oxide to quench the photocurrent of QDs via copper ion-induced formation of exciton trapping. The formed exciton trapping blocks the escape of photoelectron and thus leads to a "signal off" PEC method for sensitive immunoassay. The proposed method shows a detectable range from 0.05 to 500 ng/mL for alpha-fetoprotein (AFP) with a detection limit (LOD) of 0.038 ng/mL. This work further extends the application of exciton trapping-based PEC biosensing strategy in bioanalysis. The sensitive analytical performance of the designed route implies a promising potential of the PEC sensing in clinical diagnosis. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:496 / 500
页数:5
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