A sandwich-type electrochemical immunosensor based on in situ silver deposition for determination of serum level of HER2 in breast cancer patients

被引:103
作者
Shamsipur, Mojtaba [1 ]
Emami, Mandi [2 ]
Farzin, Leila [3 ]
Saber, Reza [4 ]
机构
[1] Razi Univ, Dept Chem, Kermanshah, Iran
[2] Univ Tehran, Univ Coll Sci, Sch Chem, Tehran, Iran
[3] Nucl Sci & Technol Res Inst, Radiat Applicat Res Sch, Tehran, Iran
[4] Univ Tehran Med Sci, Sch Adv Technol Med, Dept Nanotechnol, Tehran, Iran
关键词
Breast cancer biomarker; Electrochemical immunosensor; Signal amplification; Silver differential pulse voltammetric stripping signal; GOLD NANOPARTICLES; IMMUNOASSAY; ELECTRODE; SIGNAL; ENHANCEMENT; MATRIX; ACID;
D O I
10.1016/j.bios.2017.12.022
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The sensitive quantification of Human Epidermal growth factor Receptor 2 (HER2), as a key prognostic tumor marker, plays a critical role in screening, early diagnosis and management of breast cancer. This paper describes a sandwich-type immunoassay with silver signal enhancement strategy for highly sensitive detection of HER2. For this purpose, the target capturing step was designed by functionalization of 3-aminopropyltrimethoxysilane coated magnetite nanoparticles with antibody (antiHER2/APTMS-Fe3O4), as a platform bioconjugate (PB), and immobilized at a bare GCE. Then, in the presence of label-free immunosensor, the PB was covered by magnetic gold nanoparticles self-assembled with thiolated antibodies (antiHER2/Hyd@AuNPs-APTMS-Fe3O4) containing chemically reduced silver ions, as a label bioconjugate (LB). Under optimum conditions, a linear relationship between the differential pulse voltammetric (DPV) stripping signal of silver and the logarithm of HER2 concentrations was obtained in the range of 5.0 x 10(-4)-50.0 ng mL(-1) (R-2 = 0.9906) with a detection limit of 2.0 x 10(-5) ng mL(-1). The effectiveness of this protocol was evaluated experimentally through employing of designed immunosensor for detection of the serum level of tumor marker. The good consistency of the results with those obtained by the enzyme-linked immunosorbent assay (ELISA) conventional method (p-value of < 0.05) showed that this immunosensor can be applied for the testing of HER2 in clinical samples of breast cancer patients.
引用
收藏
页码:54 / 61
页数:8
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