Electrocatalytic evaluation of DNA damage by superoxide radical for antioxidant capacity assessment

► First antioxidant biosensor measuring O 2 - radical induced DNA-damage. ► NADH catalyst arisen from electrooxidation of intact adenines allowed detection. ► The lower the damage, the higher the catalyst amount and electrocatalytic NADH current. ► O 2 - and OH damaging power compared in the presenc...

Full description

Saved in:
Bibliographic Details
Published inJournal of electroanalytical chemistry (Lausanne, Switzerland) Vol. 659; no. 1; pp. 43 - 49
Main Authors Barroso, M.F., de-los-Santos-Álvarez, N., Lobo-Castañón, M.J., Miranda-Ordieres, A.J., Delerue-Matos, C., Oliveira, M.B.P.P., Tuñón-Blanco, P.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier B.V 01.08.2011
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:► First antioxidant biosensor measuring O 2 - radical induced DNA-damage. ► NADH catalyst arisen from electrooxidation of intact adenines allowed detection. ► The lower the damage, the higher the catalyst amount and electrocatalytic NADH current. ► O 2 - and OH damaging power compared in the presence of various antioxidants. ► CV experiments indicated that O 2 - and OH caused different lesions on DNA. The integrity of DNA purine bases was herein used to evaluate the antioxidant capacity. Unlike other DNA-based antioxidant sensors reported so far, the damaging agent chosen was the O 2 - radical enzymatically generated by the xanthine/xanthine oxidase system. An adenine-rich oligonucleotide was adsorbed on carbon paste electrodes and subjected to radical damage in the presence/absence of several antioxidant compounds. As a result, partial damage on DNA was observed. A minor product of the radical oxidation was identified by cyclic voltammetry as a diimine adenine derivative also formed during the electrochemical oxidation of adenine/guanine bases. The protective efficiency of several antioxidant compounds was evaluated after electrochemical oxidation of the remaining unoxidized adenine bases, by measuring the electrocatalytic current of NADH mediated by the adsorbed catalyst species generated. A comparison between O 2 - and OH radicals as a source of DNA lesions and the scavenging efficiency of various antioxidant compounds against both of them is discussed. Finally, the antioxidant capacity of beverages was evaluated and compared with the results obtained with an optical method.
Bibliography:http://dx.doi.org/10.1016/j.jelechem.2011.04.022
ISSN:1572-6657
1873-2569
DOI:10.1016/j.jelechem.2011.04.022