Voltammetric and spectral characterization of two flavonols for assay-dependent antioxidant capacity

被引:63
作者
He, Jian-Bo [1 ]
Yuan, Sheng-Jie [1 ]
Du, Jia-Qj [1 ]
Hu, Xin-Ran [1 ]
Wang, Yan [1 ]
机构
[1] Hefei Univ Technol, Sch Chem Engn, MOE ERC Bioproc, Anhui Key Lab Controllable Chem React & Mat Chem, Hefei 230009, Peoples R China
基金
中国国家自然科学基金;
关键词
Antioxidant capacity; ABTS radical; Hydrogen peroxide; UV-Vis spectroelectrochemistry; Flavonol; ELECTROCHEMICAL OXIDATION; CYCLIC VOLTAMMETRY; QUERCETIN; VOLTABSORPTOMETRY; KAEMPFEROL; PHENOLICS; PRODUCTS; RUTIN; MORIN; ACID;
D O I
10.1016/j.bioelechem.2009.02.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Polyphenolic compounds usually showed different antioxidant capacities depending on the assay methods used. To determine the possible chemical cause for this assay-dependence, two flavonols, kaempferol and morin, were selected as the model molecules for the comparative investigation between electrochemical and chemical oxidations. The electro-oxidation of the flavonols was studied using cyclic voltammetry and in situ UV-Vis spectroelectrochemical technique with a long-optical-path thin-layer electrolytic cell. The spectral changes recorded in different potentials were compared with those in the chemical oxidation by H2O2 or ABTS(center dot+) radical in the same thin-layer cell. The 4'-OH group of either sample was first oxidized at lower potentials or induced by H2O2, and in this case kaempferol was somewhat more active than morin. With an additional 2'-OH group, morin underwent the secondary oxidation in moderately higher potentials or by ABTS(center dot+), showing antioxidant capacity about twice of that of kaempferol. This study clarified that the chemical oxidation of a polyphenolic compound by the oxidants with different reactivities, which corresponded to its electro-oxidation in different anodic peaks, had a difference in number of oxidizable OH-groups. leading to the difference in antioxidant capacity. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:110 / 116
页数:7
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