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Label-free microfluidic paper-based electrochemical aptasensor for ultrasensitive and simultaneous multiplexed detection of cancer biomarkers.

Authors :
Wang, Yang
Luo, Jinping
Liu, Juntao
Sun, Shuai
Xiong, Ying
Ma, Yuanyuan
Yan, Shi
Yang, Yue
Yin, Huabing
Cai, Xinxia
Source :
Biosensors & Bioelectronics. Jul2019, Vol. 136, p84-90. 7p.
Publication Year :
2019

Abstract

Simultaneous detection of multiple tumor biomarkers in body fluids could facilitate early diagnosis of lung cancer, so as to provide scientific reference for clinical treatment. This paper depicted a multi-parameter paper-based electrochemical aptasensor for simultaneous detection of carcinoembryonic antigen (CEA) and neuron-specific enolase (NSE) in a clinical sample with high sensitivity and specificity. The paper-based device was fabricated through wax printing and screen-printing, which enabled functions of sample filtration and sample auto injection. Amino functional graphene (NG)-Thionin (THI)- gold nanoparticles (AuNPs) and Prussian blue (PB)- poly (3,4- ethylenedioxythiophene) (PEDOT)- AuNPs nanocomposites were synthesized respectively. They were used to modify the working electrodes not only for promoting the electron transfer rate, but also for immobilization of the CEA and NSE aptamers. A label-free electrochemical method was adopted, enabling a rapid simple point-of-care testing. Experimental results showed that the proposed multi-parameter aptasensor exhibited good linearity in ranges of 0.01–500 ng mL−1 for CEA (R2 = 0.989) and 0.05–500 ng mL−1 for NSE (R2 = 0.944), respectively. The limit of detection (LOD) was 2 pg mL−1 for CEA and 10 pg mL−1 for NSE. In addition, the device was evaluated using clinical serum samples and received a good correlation with large electrochemical luminescence (ECL) equipment, which would offer a new platform for early cancer diagnostics, especially in those resource-limit areas. • The aptasensor could enable simultaneous detection of two tumor markers in a single sample with high sensitivity. • The aptasensor had a fast response time as a label-free electrochemical detection method was adopted. • The aptasensor was fabricated by wax printing and screen-printing, which could be mass-produced easily with low cost. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09565663
Volume :
136
Database :
Academic Search Index
Journal :
Biosensors & Bioelectronics
Publication Type :
Academic Journal
Accession number :
136563638
Full Text :
https://doi.org/10.1016/j.bios.2019.04.032