Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/105469
Title: DNA Electrochemical Biosensors for In Situ Probing of Pharmaceutical Drug Oxidative DNA Damage
Authors: Chiorcea-Paquim, Ana Maria 
Oliveira-Brett, Ana Maria 
Keywords: DNA electrochemical biosensor; oxidative DNA damage; damage to DNA bases; biomarker of DNA damage; voltammetry; DNA oxidation; 8-oxoguanine (8-oxoG); 8-oxo- 20-deoxyguanosine (8-oxodG); 2,8-dihydroxyadenine (2,8-DHA)
Issue Date: 5-Feb-2021
Publisher: MDPI
Project: UID/EMS/00285/2020 
Serial title, monograph or event: Sensors (Switzerland)
Volume: 21
Issue: 4
Abstract: Deoxyribonucleic acid (DNA) electrochemical biosensors are devices that incorporate immobilized DNA as a molecular recognition element on the electrode surface, and enable probing in situ the oxidative DNA damage. A wide range of DNA electrochemical biosensor analytical and biotechnological applications in pharmacology are foreseen, due to their ability to determine in situ and in real-time the DNA interaction mechanisms with pharmaceutical drugs, as well as with their degradation products, redox reaction products, and metabolites, and due to their capacity to achieve quantitative electroanalytical evaluation of the drugs, with high sensitivity, short time of analysis, and low cost. This review presents the design and applications of label-free DNA electrochemical biosensors that use DNA direct electrochemical oxidation to detect oxidative DNA damage. The DNA electrochemical biosensor development, from the viewpoint of electrochemical and atomic force microscopy (AFM) characterization, and the bottom-up immobilization of DNA nanostructures at the electrode surface, are described. Applications of DNA electrochemical biosensors that enable the label-free detection of DNA interactions with pharmaceutical compounds, such as acridine derivatives, alkaloids, alkylating agents, alkylphosphocholines, antibiotics, antimetabolites, kinase inhibitors, immunomodulatory agents, metal complexes, nucleoside analogs, and phenolic compounds, which can be used in drug analysis and drug discovery, and may lead to future screening systems, are reviewed.
URI: https://hdl.handle.net/10316/105469
ISSN: 1424-8220
DOI: 10.3390/s21041125
Rights: openAccess
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
I&D CEMMPRE - Artigos em Revistas Internacionais

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