A SERS-based immunoassay for the detection of α-fetoprotein using AuNS@Ag@SiO2 core-shell nanostars

被引:35
|
作者
Zhao, Jing [1 ]
Wu, Chen [1 ]
Zhai, Lipeng [2 ]
Shi, Xiaofeng [3 ]
Li, Xin [1 ]
Weng, Guojun [1 ]
Zhu, Jian [1 ]
Li, Jianjun [1 ]
Zhao, Jun-Wu [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Key Lab Biomed Informat Engn, Minist Educ, Xian 710049, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Sci, Dept Phys, Xian 710049, Shaanxi, Peoples R China
[3] Xian Municipal Res Inst Environm Protect, Xian 710049, Shaanxi, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
ENHANCED RAMAN-SCATTERING; HEPATOCELLULAR-CARCINOMA; SILVER NANOPARTICLES; GRAPHENE OXIDE; GOLD NANOSTARS; NANOSTRUCTURE; SENSITIVITY; IMPROVE; GLUCOSE; DESIGN;
D O I
10.1039/c9tc01890e
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A surface-enhanced Raman scattering (SERS)-based sandwich type immunoassay was developed for the detection of alpha-fetoprotein (AFP) with high sensitivity, reproducibility and selectivity. In the immunoassay, an antibody immobilized nitrocellulose (NC) membrane was employed to capture AFP and antibody conjugated silica coated gold/silver core-shell nanostars (AuNS@Ag@SiO2) were used as SERS probes. AuNS@Ag was synthesized by the direct deposition of Ag on the AuNS. The Ag shell grew outward from the center towards the tips and adopted a polyhedral shape. The AuNS@Ag nanoparticles were shown to have higher SERS activity than gold nanostars (AuNSs), and their LSPR wavelengths could be finely tuned across a wide spectrum ranging from visible to near-infrared by simply adjusting the Ag shell thickness. The silica coating improved colloidal stability of the nanostructure and provided functionality for antibody conjugation. By using 4-mercaptobenzoic acid (4-MBA) as a Raman reporter molecule, the proposed SERS sensor is able to detect AFP with a low limit of detection (LOD) of 0.72 pg mL(-1) and a wide and clinically relevant linear detection range from 3 pg mL(-1) to 3 mu g mL(-1). Hence, this SERS-based immunoassay provides a strategy for the detection of trace AFP and has potential to assist in the monitoring of prognosis for hepatocellular carcinoma (HCC) patients.
引用
收藏
页码:8432 / 8441
页数:10
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