Detection of the potential tumor marker of AFP using surface-enhanced Raman scattering-based immunoassay

被引:39
作者
Wang, Aijing [1 ,2 ]
Ruan, Weidong [1 ]
Song, Wei [1 ]
Chen, Lei [1 ]
Zhao, Bing [1 ]
Jung, Young Mee [2 ]
Wang, Xu [1 ]
机构
[1] Jilin Univ, State Key Lab Supramol Struct & Mat, Changchun 130012, Peoples R China
[2] Kangwon Natl Univ, Dept Chem, Inst Mol Sci & Fus Technol, Chunchon 200701, South Korea
基金
新加坡国家研究基金会;
关键词
surface-enhanced Raman scattering (SERS); -fetoprotein (AFP); gold nanoparticles (AuNPs); immunoassay; sandwich type assay; GOLD NANOPARTICLES; ANTIGEN; SERS; SPECTROSCOPY; RESONANCE; IMMUNOSENSOR; FLUORESCENCE; ANTIBODY; BINDING; DESIGN;
D O I
10.1002/jrs.4391
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The development of rapid, highly sensitive detection methods for -fetoprotein (AFP) is very important. As hepatocellular carcinoma is closely related to the level of AFP in the blood, it is necessary to maintain an AFP concentration below the safety limit. In this paper, we propose a universal, rapid, sensitive, and highly specific immunoassay system utilizing gold nanoparticles (AuNPs) and surface-enhanced Raman scattering (SERS). This new system features a sandwich structure combining mercaptobenzoic acid-labeled immunogold nanoparticles with the antigen and the antibody atop a pre-designed substrate made of a glass slide modified with AuNPs. This SERS-based immunoassay can detect AFP concentrations as low as 100pg/ml, which is a significant improvement on the capabilities of the enzyme-linked immunosorbent assay method. A good linear relationship between the SERS peak intensity and the logarithm of antigen concentrations (from 1ng/ml to 100ng/ml) was observed. This technique provides an effective model for the detection of biomarkers in medical diagnostics, criminal investigation, and other fields. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:1649 / 1653
页数:5
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