An enzyme-mediated competitive colorimetric sensor based on Au@Ag bimetallic nanoparticles for highly sensitive detection of disease biomarkers

被引:44
作者
Yin, Binfeng [1 ,2 ,3 ]
Zheng, Wenshu [1 ,2 ,4 ]
Dong, Mingling [1 ,2 ]
Yu, Wenbo [1 ,2 ]
Chen, Yiping [1 ,2 ]
Joo, Sang Woo [3 ]
Jiang, Xingyu [1 ,2 ,4 ]
机构
[1] Natl Ctr NanoSci & Technol, CAS Ctr Excellence Nanosci, Beijing Engn Res Ctr BioNanotechnol, Beijing 100190, Peoples R China
[2] Natl Ctr NanoSci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Biol Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
[3] Yeungnam Univ, Sch Mech Engn, Gyongsan 712749, South Korea
[4] Univ Chinese Acad Sci, 19 A Yuquan Rd, Beijing 100049, Peoples R China
基金
新加坡国家研究基金会; 美国国家科学基金会;
关键词
FUNCTIONALIZED GOLD NANOPARTICLES; NANOMOLAR LEVEL; NAKED EYE; ASSAY; NANOMATERIALS; IMMUNOASSAY; CATALASE; STRATEGY; ACETYLCHOLINESTERASE; DIAGNOSTICS;
D O I
10.1039/c7an00779e
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We developed a competitive colorimetric nanosensor based on Au@Ag bimetallic nanoparticles for the detection of interleukin-6 (IL-6) in clinical samples. Antibody-conjugated magnetic nanoparticles (MNPs) and polystyrene (PS) microparticles conjugated with both catalase and a secondary antibody can form sandwich structures that enable one-step target enrichment and separation. The catalase on the surface of the PS can catalyze the hydrolysis of hydrogen peroxide (H2O2) to regulate the deposition of Ag+ on the surface of gold nanoparticles (AuNPs), and forms different sizes and amounts of Au@Ag bimetallic nanoparticles (Au@AgNPs) which produce a distinct color signal for readout with the naked eye. Our sensor features high sensitivity, selectivity, reproducibility and anti-interference property as a result of comprehensive parameter optimization. The limit of detection of IL-6 can reach 11 pg mL(-1) with the naked eye and 1.2 pg mL(-1) by quantitative instrumental analysis. The whole analysis can be finished within 1 h. More importantly, we successfully apply our platform or the detection of IL-6 in clinical samples with better accuracy than conventional enzyme-linked immunosorbent assay (ELISA).
引用
收藏
页码:2954 / 2960
页数:7
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