Dual-signal amplified electrochemiluminescence immunoassay for salbutamol based on quantum dots and gold nanoparticle-labeled horseradish peroxidase

被引:20
作者
Cai, Fudong [1 ,2 ]
Wang, Nan [1 ,2 ]
Dong, Tiantian [1 ,2 ]
Deng, Anping [1 ,2 ]
Li, Jianguo [1 ,2 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[2] Key Lab Hlth Chem & Mol Diag Suzhou, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
COUPLING ENZYMATIC AMPLIFICATION; ULTRASENSITIVE DETECTION; ELECTROGENERATED CHEMILUMINESCENCE; MASS-SPECTROMETRY; IMMUNOSENSOR; CHROMATOGRAPHY; CLENBUTEROL; FABRICATION; URINE;
D O I
10.1039/c5an00999e
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This study describes a novel electrochemical immunosensor to amplify the electrochemiluminescence (ECL) signal for the ultrasensitive detection of salbutamol (SAL) using quantum dots (QDs) and gold nano-particle (AuNP) conjugated horseradish peroxidase (HRP). The electrochemical detection was based on the HRP catalyzed consumption of self-produced H2O2, which has been extensively used as a co-reactant of QDs, by o-phenylenediamine (OPD). The enzymatic reaction rate is proportional to the amount of HRP bound to the electrode. In the presence of a SAL standard solution, the immobilized SAL coating antigens competed with the SAL solution for the Ab-AuNPs-HRP complexes. With an increase in the SAL concentration, the amount of immobilized HRP decreases, which leads to an increase in the ECL intensity. Under optimized conditions, the ECL intensity changes linearly with the logarithm of the SAL concentration in the range of 0.05-500 ng mL(-1) with a detection limit of 0.017 ng mL(-1) (S/N = 3). The ECL immunosensor possesses high sensitivity, satisfactory reproducibility and selectivity, and may provide a feasible route for practical application.
引用
收藏
页码:5885 / 5890
页数:6
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