Electrochemical detection of DNA damage induced by clenbuterol at a reduced graphene oxide-Nafion modified glassy carbon electrode. Issue 7 (3rd February 2017)

• Record Type: Journal Article
• Authors: Lin, Xiaoyun; Ni, Yongnian; Pei, Xueying; Kokot, Serge
• Is Part Of: Analytical methods. Volume 9:Issue 7(2017)
• Page Start: 1105
• Page End: 1111
• Publication Date: 2017-02-03
• Subjects: Chemistry, Analytic -- Periodicals; Analytical biochemistry -- Periodicals; Chemical laboratories -- Standards -- Periodicals; 543.1905
• DOI: 10.1039/c6ay03022j
• Languages: English
• ISSNs: 1759-9660

Abstract

Abstract : An electrochemical biosensor (dsDNA/RGO-Nafion/GCE) was developed for direct detection of DNA damage induced by clenbuterol and analysis of clenbuterol indirectly. Abstract : An electrochemical biosensor capable of direct detection of DNA damage induced by clenbuterol (CLB) has been developed. A glassy carbon electrode (GCE) was modified using reduced graphene oxide-Nafion and dsDNA to produce a dsDNA/RGO-Nafion/GCE sensor. The modified electrode was characterized by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV), and the results at each stage of the electrode construction were interpreted. They indicated that the electrochemical oxidation peak currents of guanine and adenine at the electrode (dsDNA/RGO-Nafion/GCE) significantly increased as compared with those at the untreated electrode (dsDNA/GCE). Based on this, the sensor was used to measure the change of the oxidation peak currents for guanine and adenine between the intact and damaged dsDNA in the sensor films, and the DNA damage was successfully detected. Furthermore, the plot of peak current decline for the guanine and adenine versus the concentration of CLB was linear in the range of 5.0 × 10 −7 to 4.0 × 10 −6 mol L −1, with a limit of detection (LOD) of 3.2 × 10 −7 mol L −1, which provided a good method to determine CLB indirectly.