Kinetic evaluation of the reactivity of flavonoids as radical scavengers

被引:31
作者
Fujisawa, S
Ishihara, M
Kadoma, Y
机构
[1] Meikai Univ, Sch Dent, Dept Oral Diag, Sakado, Saitama 3500283, Japan
[2] Meikai Univ, Sch Dent, Dept Chem, Sakado, Saitama 3500283, Japan
[3] Tokyo Med & Dent Univ, Div Biofunct Mol, Inst Biomat & Bioengn, Tokyo 1010062, Japan
关键词
flavonoids; radical scavenging activity; stoichiometric factors; induction period; inhibition rate constants; frontier orbital theory;
D O I
10.1080/1062936021000020071
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(T)he reactivity of flavonoids as radical scavengers was investigated under kinetic considerations using radical polymerization of methyl methacrylates initiated by benzoyl peroxide. The number of radicals which are trapped by each molecule of phenol (the stoichiometric factors, n values) decreased in the order of epigallocatechin-3-O-gallate (ECG) (5.5) > catechin (3.5) > resveratrol (2.4) > quercetin (1.9) > n-propylgallate (1.5) > hesperetin (1.0). The inhibition rate constants (k(inh)) (I - 3 X 10(3)1/(mol s)) for the flavonoids were not different from each other, and, therefore, the radical scavenging activity depend on n values. The n values of the fully oxidized flavonoids were estimated from the frontier orbital theory, using PM3 semiempirical molecular orbital calculation. The experimental n values were consistent with the calculated values.
引用
收藏
页码:617 / 627
页数:11
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