Abstract
In this study, we developed a highly sensitive and selective electrochemical biosensor for the detection of the specific-sequence target DNA. It was fabricated based on a “sandwich-type” detection strategy, which involved capture probe immobilized on the surface of the gold nanorods (Au NRs) decorated reduced graphene oxide (rGO) sheets, and reporter probe labeled gold nanoparticle (Au NPs) that flank the target DNA. Adriamycin was used as an electrochemical indicator because it could be electrostatically bonded to the anionic phosphate of DNA strands. Differential pulse voltammetry (DPV) was used to investigate the hybridization event by the measurements of peak current of adriamycin changed before and after hybridization. The incorporation of Au NPs and Au NRs decorated rGO sheets in this sensor design significantly enhanced the sensing performance. Under optimal conditions, the peak currents of adriamycin in DPV were linear with the logarithm of target DNA concentration in the range of 1.0×10−16 to 1.0×10−9M with a detection limit of 3.5×10−17M (signal/noise ratio of 3). In addition, this DNA sensor exhibited good selectivity, even for single-base mismatched target DNA detection.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
