An enzyme-induced Au@Ag core-shell nanoStructure used for an ultrasensitive surface-enhanced Raman scattering immunoassay of cancer biomarkers

被引:64
作者
Yang, Lin [1 ]
Gao, Ming Xuan [2 ]
Zhan, Lei [1 ]
Gong, Min [3 ]
Zhen, Shu Jun [2 ]
Huang, Cheng Zhi [1 ]
机构
[1] Southwest Univ, Key Lab Luminescence & Real Time Analyt Chem, Minist Educ, Coll Pharmaceut Sci, Chongqing 400715, Peoples R China
[2] Southwest Univ, Chongqing Key Lab Biomed Anal, Chongqing Sci & Technol Commiss, Coll Chem & Chem Engn, Chongqing 400715, Peoples R China
[3] Inst Surg Res, Daping Hosp, Dept Pathol, Chongqing 400042, Peoples R China
基金
中国国家自然科学基金;
关键词
SIGNAL AMPLIFICATION STRATEGY; ALPHA-FETOPROTEIN; LUNG-CANCER; SERS; NANOPARTICLES; SPECTROSCOPY; FABRICATION; MARKERS; ARRAY; DOTS;
D O I
10.1039/c6nr07979b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Early detection of cancer is helpful for the control and prevention of diseases. Due to the low content of cancer biomarkers in the early disease phases, however, an ultrasensitive and selective method is critical. In this contribution, an ultrasensitive surface-enhanced Raman scattering (SERS) immunoassay is newly developed with the principle of introducing a common enzyme-induced deposition (EID) reaction to coat a silver layer on the surface of gold nanoparticles and to form a core-shell nanostructure of Au@Ag. By using alkaline phosphatase (ALP) to dephosphorylate its substrate, 2-phospho-L-ascorbic acid trisodium salt (AAP), to form vitamin C, silver ions could be reduced into silver atoms and coated on the surface of the AuNPs; a greatly enhanced SERS signal was then obtained. As a proof of concept, alpha-fetoprotein (AFP) was detected as a target, which is a biomarker of liver cancer. Excellent analytical performance of the SERS immunoassay could be achieved in the range from 0.5 to 100 pg mL(-1) with a limit of detection of 0.081 pg mL(-1) (3 sigma). Identical results could be obtained by using the newly proposed SERS immunoassay for the clinical detection of AFP in serum samples of patients to those clinically obtained by chemiluminescence immunoassays, demonstrating the potential applications of the developed method in clinical diagnosis.
引用
收藏
页码:2640 / 2645
页数:6
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