Loading…
Highly sensitive and label-free electrochemical biosensor based on gold nanostructures for studying the interaction of prostate cancer gene sequence with epirubicin anti-cancer drug
[Display omitted] •Graphite screen printed electrodes modified with AuNCs and ds-DNA as a new biosensor.•The prepared biosensor was successfully used as stable device for EPI detection.•Other cancer drugs have no interference to determine the EPI in this biosensor.•Proposed biosensor has simple fabr...
Saved in:
Published in: | Microchemical journal 2021-11, Vol.170, p.106668, Article 106668 |
---|---|
Main Authors: | , , , |
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!
|
Summary: | [Display omitted]
•Graphite screen printed electrodes modified with AuNCs and ds-DNA as a new biosensor.•The prepared biosensor was successfully used as stable device for EPI detection.•Other cancer drugs have no interference to determine the EPI in this biosensor.•Proposed biosensor has simple fabrication, high sensitivity and rapid response.
A label-free electrochemical DNA hybridization biosensor was developed based on gold nanocubes (AuNCs) modified graphite screen-printed electrodes (GSPEs) for investigating the epirubicin (EPI) interaction with the short sequence DNA of prostate cancer gene. The electrochemical behavior of the genosensor was assessed in different steps of construction using cyclic voltammetry and electrochemical impedance spectroscopy methods. The changes in the biosensor responses versus the DNA interactions with the various concentrations of EPI were monitored by the differential pulse voltammetry method. The reduction peak current of EPI linearly increased with the increasing concentration of EPI. Under optimal conditions, two linear ranges were obtained from 0.04 to 0.80 μM and 0.8 to 20.0 μM, respectively with a limit of detection 0.01 μM. The prepared biosensor exhibited a proper selectivity toward the target drugs. The applicability of the sensor was demonstrated by the explored of epirubicin in a human blood serum sample. In addition, the prepared biosensor was used as a reproducible and stable device for EPI determination. |
---|---|
ISSN: | 0026-265X 1095-9149 |
DOI: | 10.1016/j.microc.2021.106668 |