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dc.contributor.authorApak, Resat
dc.contributor.authorBeker, Bilge Yildogan
dc.contributor.authorBakir, Temelkan
dc.contributor.authorSÖNMEZOĞLU, İnci
dc.contributor.authorImer, Filiz
dc.date.accessioned2021-03-03T19:39:13Z
dc.date.available2021-03-03T19:39:13Z
dc.date.issued2011
dc.identifier.citationBeker B. Y. , Bakir T., SÖNMEZOĞLU İ., Imer F., Apak R., "Antioxidant protective effect of flavonoids on linoleic acid peroxidation induced by copper(II)/ascorbic acid system", CHEMISTRY AND PHYSICS OF LIPIDS, cilt.164, sa.8, ss.732-739, 2011
dc.identifier.issn0009-3084
dc.identifier.otherav_55c1107f-d6b2-4a86-9b5a-cd0a8802090a
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/60567
dc.identifier.urihttps://doi.org/10.1016/j.chemphyslip.2011.09.001
dc.description.abstractAntioxidants are compounds that can delay or inhibit lipid oxidation. The peroxidation of linoleic acid (LA) in the absence and presence of Cu(II) ion-ascorbate combinations was investigated in aerated and incubated emulsions at 37 degrees C and pH 7. LA peroxidation induced by copper(II)-ascorbic acid system followed first order kinetics with respect to hydroperoxides concentration. The extent of copper-initiated peroxide production in a LA system assayed by ferric thiocyanate method was used to determine possible antioxidant and prooxidant activities of the added flavonoids. The effects of three different flavonoids of similar structure, i.e. quercetin (QR), morin (MR) and catechin (CT), as potential antioxidant protectors were studied in the selected peroxidation system. The inhibitive order of flavonoids in the protection of LA peroxidation was: morin > catechin >= quercetin, i.e. agreeing with that of formal reduction potentials versus NHE at pH 7, i.e. 0.60, 0.57 and 0.33 V for MR, CT, and QR. respectively. Morin showed antioxidant effect at all concentrations whereas catechin and quercetin showed both antioxidant and prooxidant effects depending on their concentrations. The structural requirements for antioxidant activity in flavonoids interestingly coincide with those for Cu(II)-induced prooxidant activity, because as the reducing power of a flavonoid increases, Cu(II)-Cu(I) reduction is facilitated that may end up with the production of reactive species. The findings of this study were evaluated in the light of structure-activity relationships of flavonoids, and the results are believed to be useful to better understand the actual conditions where flavonoids may act as prooxidants in the preservation of heterogeneous food samples containing traces of transition metal ions. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
dc.language.isoeng
dc.subjectSitogenetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectBİYOFİZİK
dc.subjectBiyoloji ve Biyokimya
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyofizik
dc.subjectBiyokimya
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.titleAntioxidant protective effect of flavonoids on linoleic acid peroxidation induced by copper(II)/ascorbic acid system
dc.typeMakale
dc.relation.journalCHEMISTRY AND PHYSICS OF LIPIDS
dc.contributor.departmentYıldız Teknik Üniversitesi , ,
dc.identifier.volume164
dc.identifier.issue8
dc.identifier.startpage732
dc.identifier.endpage739
dc.contributor.firstauthorID202246


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