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dc.contributor.authorUzunboy, Seda
dc.contributor.authorEksin, Ece
dc.contributor.authorErdem, Arzum
dc.contributor.authorApak, Resat
dc.contributor.authorCekic, Sema Demirci
dc.date.accessioned2021-03-05T15:19:33Z
dc.date.available2021-03-05T15:19:33Z
dc.identifier.citationUzunboy S., Cekic S. D. , Eksin E., Erdem A., Apak R., "CUPRAC colorimetric and electroanalytical methods determining antioxidant activity based on prevention of oxidative DNA damage", ANALYTICAL BIOCHEMISTRY, cilt.518, ss.69-77, 2017
dc.identifier.issn0003-2697
dc.identifier.otherav_bb5bb443-cc79-4895-a219-77334509cf08
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/124565
dc.identifier.urihttps://doi.org/10.1016/j.ab.2016.10.028
dc.description.abstractAn unbalanced excess of oxygen/nitrogen species (ROS/RNS) can give oxidative hazard to DNA and other biomacromolecules under oxidative stress conditions. While the 'comet' assay for measuring DNA damage is neither specific nor practical, monitoring oxidative changes on individual DNA bases and other oxidation products needs highly specialized equipment and operators. Thus, we developed a modified CUPRAC (cupric ion reducing antioxidant capacity) colorimetric method to determine the average total damage on DNA produced by Fenton oxidation, taking advantage of the fact that the degradation products of DNA but not the original macromolecule is CUPRAC responsive. The DNA protective effects of water-soluble antioxidants were used to devise a novel antioxidant activity assay, considered to be physiologically more realistic than those using artificial probes. Our method, based on the measurement of DNA oxidative products with CUPRAC colorimetry proved to be 2 orders-of-magnitude more sensitive than the widely used TBARS (thiobarbituric acid-reactive substances) colorimetric assay used as reference. Additionally, the DNA damage was electrochemically investigated using pencil graphite electrodes (PGEs) as DNA sensor platform in combination with differential pulse voltammetry (DPV). The interaction of the radical species with DNA in the absence/presence of antioxidants was detected according to the changes in guanine oxidation signal. (C) 2016 Elsevier Inc. All rights reserved.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectKimya
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectAnalitik Kimya
dc.subjectTemel Bilimler
dc.subjectBİYOKİMYASAL ARAŞTIRMA YÖNTEMLERİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectKİMYA, ANALİTİK
dc.subjectTemel Bilimler (SCI)
dc.titleCUPRAC colorimetric and electroanalytical methods determining antioxidant activity based on prevention of oxidative DNA damage
dc.typeMakale
dc.relation.journalANALYTICAL BIOCHEMISTRY
dc.contributor.departmentEge Üniversitesi , ,
dc.identifier.volume518
dc.identifier.startpage69
dc.identifier.endpage77
dc.contributor.firstauthorID11476


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