Abstract

Simplification and miniaturisation of analytical methods for the direct detection of DNA damage is a challenging area of research and screen-printed electrodes are a promising alternative approach to analytically/electroanalytically monitor the species involved. In this work we demonstrate that screen-printed graphite macroelectrodes (SPEs) provide useful electrochemical signatures to study the behaviour of 8-oxoguanine (8-oxoGua), which is the most frequent and important marker of oxidative DNA damage and it is widely considered as a biomarker, via differential pulse voltammetry (DPV). Under the optimum experimental conditions, the proposed electrochemical sensing protocol towards 8-oxoGua using SPEs is demonstrated to be possible over the concentration range of 0.1–12μM. The response of the SPEs is superior over routinely utilised glassy carbon electrodes in terms of sensitivity with a limit of detection (3σ) found to correspond to 0.33μM. Reproducibility and repeatability of the proposed methodology at low and high concentrations were also demonstrated. Quantification of 8-oxoGua in the presence of other nucleobases and different compounds of interest which are present in biological fluids was successfully accomplished. Furthermore, proof-of-concept demonstrating the potential use of the developed SPE based methodology for the detection of 8-oxoGua in real complex samples as demonstrated in simulated biological samples (human semen).

Full Text
Paper version not known

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 call

Disclaimer: 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.