Automated and ultrasensitive detection of methyl-3-quinoxaline-2-carboxylic acid by using gold nanoparticles probes SIA-rt-PCR

被引:32
作者
Chen, Wei [2 ]
Jiang, Yuan [3 ]
Ji, Baoqing [2 ]
Zhu, Changqin [3 ]
Liu, Liqiang [2 ]
Peng, Chifang [2 ]
Jin, M. Kim [2 ]
Qiao, Ruirui [4 ]
Jin, Zhengyu [2 ]
Wang, Libing [2 ]
Zhu, Shuifang [1 ]
Xu, Chuanlai [2 ]
机构
[1] Chinese Acad Inspect & Quarantine, Beijing 10008, Peoples R China
[2] Jiangnan Univ, Sch Food Sci & Technol, Wuxi 214122, Jiangsu, Peoples R China
[3] Jiangsu Import & Export Inspect & Quarantine Bur, Food Lab, Nanjing 210000, Jiangsu, Peoples R China
[4] Chinese Acad Sci, Inst Chem, Beijing 10008, Peoples R China
基金
中国国家自然科学基金;
关键词
MQCA; Gold; Superparamagnetic nanoparticles; Sequential injection analysis; rt-PCR; SENSITIVE ANTIGEN-DETECTION; SEQUENTIAL INJECTION; IMMUNO-PCR; DNA; QUANTIFICATION; ASSAY; NANOSTRUCTURES;
D O I
10.1016/j.bios.2009.02.015
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
An ultrasensitive and rapid sequential injection analysis (SIA) based on real-time PCR (SIA-rt-PCR) assay was developed by using different nanoparticles for the detection of small molecule chemicals residues. Gold (Au) nanoparticle, conjugated with goat anti-rabbit IgG and duplex strand DNA (dsDNA), was used as a substitute for chemiluminescent probes in an SIA system. By indirect competitive immunoreactions in the SIA system, the gold nanoparticles were attached to antigens which were immobilized by superparamagnetic nanoparticles (SMNPs). The dsDNA on the gold nanoparticles was dehybridized and then the single-stranded DNA (ssDNA) was collected and quantified with rt-PCR, which showed a rather low linearity range from 2.5 atto mol L-1 (aM) to 250 femto mol L-1 (fM) and the LOD was 1.4 aM. This method, which is rapid, automated and capable of high-throughput, was used to detect methyl-3-quinoxaline-2-carboxylic acid (MQCA) residues in real samples. The analytical results had a coefficient of variation of less than 15% and the recovery was 89-108%. Crown Copyright (C) 2009 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2858 / 2863
页数:6
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