Highly sensitive detection of clenbuterol using competitive surface-enhanced Raman scattering immunoassay

被引:92
作者
Zhu, Guichi
Hu, Yongjun [1 ]
Gao, Jiao
Zhong, Liang
机构
[1] S China Normal Univ, Coll Biophoton, MOE Key Lab Laser Life Sci, Guangzhou 510631, Guangdong, Peoples R China
关键词
Clenbuterol; Surface-enhanced Raman scattering; Competitive; Label; Immunoassay; SPECTROSCOPIC DETECTION; LIQUID-CHROMATOGRAPHY; MASS-SPECTROMETRY; NANOPARTICLES; MOLECULES; PLATFORM; TISSUES; LABELS; URINE; FILMS;
D O I
10.1016/j.aca.2011.04.031
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this report, we present a novel approach to detect clenbuterol based on competitive surface-enhanced Raman scattering (SERS) immunoassay. Herein, a SERS nanoprobe that relies on gold nanoparticle (GNP) is labeled by 4,4'-dipyridyl (DP) and clenbuterol antibody, respectively. The detection of clenbuterol is carried out by competitive binding between free clenbuterol and clenbuterol-BSA fastened on the substrate with their antibody labeled on SERS nanoprobes. The present method allows us to detect clenbuterol over a much wider concentration range (0.1-100 pg mL(-1)) with a lower limit of detection (ca. 0.1 pg mL(-1)) than the conventional methods. Furthermore, by the use of this new competitive SERS immunoassay, the clenbuterol-BSA (antigen) is chosen to fasten on the substrate instead of the clenbuterol antibody, which could reduce the cost of the assay. Results demonstrate that the proposed method has the wide potential applications in food safety and agonist control. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 66
页数:6
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