Issue 4, 2017

An electrochemical cytosensor for ultrasensitive detection of cancer cells using modified graphene–gold nanostructures

Abstract

The ultrasensitive detection of human prostate metastatic cancer cells (Du-145) was investigated through a novel electrochemical cytosensor. The proposed biosensor was simultaneously developed via two approaches: multivalent identification and signal amplification. Herein, anti-CD166 monoclonal antibody-modified gold electrode was applied to capture and recognize target cells (Du-145). Also, a graphene (G)/gold nanoparticle (GNP)/horseradish peroxidase (HRP)-conjugated trastuzumab antibody (G/GNP/Ab-HRP) hybrid nanostructure was designed as a nanoprobe for accurate recognition of target cells and efficient amplification of enzymatic signals simultaneously. The performance of the cytosensor could be significantly improved by utilizing this novel signal-amplification strategy. The cytosensor described here exhibited an appropriate cell-capture ability, broad range of detection, and exceptional sensitivity with a low limit of detection (20 cells). The fabricated cytosensor showed high sensitivity and selectivity for detection of Du-145 cancer cells while keeping an extended linear range from 102 to 106 cells per ml, and a conveniently low limit of detection of 20 cells per ml. The extraordinary analytical performance of this cytosensor indicates that it has a great potential for the detection of cancer cells and cancer stem cells.

Graphical abstract: An electrochemical cytosensor for ultrasensitive detection of cancer cells using modified graphene–gold nanostructures

Supplementary files

Article information

Article type
Paper
Submitted
27 Oct 2016
Accepted
28 Nov 2016
First published
05 Dec 2016
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 2365-2372

An electrochemical cytosensor for ultrasensitive detection of cancer cells using modified graphene–gold nanostructures

A. Yadegari, M. Omidi, F. Yazdian, H. Zali and L. Tayebi, RSC Adv., 2017, 7, 2365 DOI: 10.1039/C6RA25938C

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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