Loading…

Ultrasensitive electrochemical biosensing platform based on spherical silicon dioxide/molybdenum selenide nanohybrids and triggered Hybridization Chain Reaction

An ultrasensitive sandwich-type electrochemical biosensor for DNA detection is developed based on spherical silicon dioxide/molybdenum selenide (SiO2@MoSe2) and graphene oxide–gold nanoparticles (GO–AuNPs) hybrids as carrier triggered Hybridization Chain Reaction (HCR) coupling with multi-signal amp...

Full description

Saved in:
Bibliographic Details
Published in:Biosensors & bioelectronics 2017-08, Vol.94, p.616-625
Main Authors: Shuai, Hong-Lei, Wu, Xu, Huang, Ke-Jing, Zhai, Zi-Bo
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:An ultrasensitive sandwich-type electrochemical biosensor for DNA detection is developed based on spherical silicon dioxide/molybdenum selenide (SiO2@MoSe2) and graphene oxide–gold nanoparticles (GO–AuNPs) hybrids as carrier triggered Hybridization Chain Reaction (HCR) coupling with multi-signal amplification. The proposed sensoring assay utilizes a spherical SiO2@MoSe2/AuNPs as sensing platform and GO–AuNPs hybrids as carriers to supply vast binding sites. H2O2+HQ system is used for DNA detection and HCR as the signal and selectivity enhancer. The sensor is designed in sandwich type to increase the specificity. As a result, the present biosensor exhibits a good dynamic range from 0.1fM to 100pM with a low detection limit of 0.068fM (S/N=3). This work shows a considerable potential for quantitative detection of DNA in early clinical diagnostics. •SiO2@MoSe2 was prepared with large specific surface area and good electro-conductivity.•SiO2@MoSe2 was used as sensing platform and GO–AuNPs hybrids as signal carriers.•H2O2+HQ system is used for DNA detecting with signal amplification.•The biosensor shows a detection limit of 0.068 fM and high specificity towards target DNA.
ISSN:0956-5663
1873-4235
DOI:10.1016/j.bios.2017.03.058