Antioxidant capacity of reaction products limits the applicability of the Trolox Equivalent Antioxidant Capacity (TEAC) assay

被引:233
作者
Arts, MJTJ [1 ]
Haenen, GRMM [1 ]
Voss, HP [1 ]
Bast, A [1 ]
机构
[1] Maastricht Univ, Fac Med, Dept Pharmacol & Toxicol, NL-6200 MD Maastricht, Netherlands
关键词
TEAC; ABTS radical; flavonoids; antioxidant; chrysin;
D O I
10.1016/j.fct.2003.08.004
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The Trolox Equivalent Antioxidant Capacity (TEAC) assay is based on the scavenging of the 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical (ABTS(.)) converting it into a colorless product. The degree of decolorization induced by a compound is related to that induced by trolox, giving the TEAC value. The assay is frequently used for constructing structure activity relationships (SARs). HPLC analysis of the reaction mixture, obtained after scavenging of ABTS(.) by the flavonoid chrysin, shows that a product is formed that also reacts with ABTS(.). The product has a higher antioxidant capacity and reacts faster with ABTS(.) than the parent compound, chrysin. In contrast to the reaction product of chrysin, the reaction product of trolox, which is formed during scavenging of ABTS(.), i.e. trolox quinone, does not react with ABTS(.). The experiments show that the TEAC is the antioxidant capacity of the parent compound plus the potential antioxidant capacity of the reaction product(s). This means that the TEAC assay does not necessarily reflect the antioxidant effect of only one structure. This hampers the applicability of the assay for the construction of SARs and for ranking antioxidants. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:45 / 49
页数:5
相关论文
共 20 条
[1]  
Aliaga C, 1998, INT J CHEM KINET, V30, P565, DOI 10.1002/(SICI)1097-4601(1998)30:8<565::AID-KIN5>3.0.CO
[2]  
2-Q
[3]   Masking of antioxidant capacity by the interaction of flavonoids with protein [J].
Arts, MJTJ ;
Haenen, GRMM ;
Voss, HP ;
Bast, A .
FOOD AND CHEMICAL TOXICOLOGY, 2001, 39 (08) :787-791
[4]   AIR OXIDATION OF HYDROCARBONS .2. THE STOICHIOMETRY AND FATE OF INHIBITORS IN BENZENE AND CHLOROBENZENE [J].
BOOZER, CE ;
HAMMOND, GS ;
HAMILTON, CE ;
SEN, JN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (12) :3233-3237
[5]  
Campos AM, 1997, INT J CHEM KINET, V29, P219
[6]   One-electron oxidation of quercetin and quercetin derivatives in protic and non protic media [J].
Dangles, O ;
Fargeix, G ;
Dufour, C .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1999, (07) :1387-1395
[7]  
DANGLES O, 2000, J CHEM SOC P2, V8, P1653
[8]  
Halliwell B, 1996, ANNU REV NUTR, V16, P33, DOI 10.1146/annurev.nu.16.070196.000341
[9]   Peroxynitrite scavenging of flavonoids: structure activity relationship [J].
Heijnen, CGM ;
Haenen, GRMM ;
Vekemans, JAJM ;
Bast, A .
ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2001, 10 (04) :199-206
[10]   Scavenging mechanisms of (-)-epigallocatechin gallate and (-)-epicatechin gallate on peroxyl radicals and formation of superoxide during the inhibitory action [J].
Kondo, K ;
Kurihara, M ;
Miyata, N ;
Suzuki, T ;
Toyoda, M .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (7-8) :855-863