Validation of a quantitative assay for the total content of lipophilic and hydrophilic antioxidants in foods

被引:27
作者
Halvorsen, Bente L. [1 ]
Blomhoff, Rune [1 ]
机构
[1] Univ Oslo, Inst Basic Med Sci, Dept Nutr, N-0316 Oslo, Norway
关键词
Antioxidants; Food; FRAP; Hydrophilic; Lipophilic; Reaction rate curves; Validation; REDUCING/ANTIOXIDANT POWER ASSAY; ABSORBENCY CAPACITY ASSAY; IN-VITRO ASSAYS; PHENOLIC-COMPOUNDS; FLAVONOIDS; BEVERAGES; DISEASE; PLASMA; FRUITS; FRAP;
D O I
10.1016/j.foodchem.2010.12.142
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
One of the main methods used to assess total antioxidant content in foods is the Ferric Reducing Ability of Plasma (FRAP) assay. The FRAP assay has previously not been extensively validated. In the present study, 39 pure compounds, such as different polyphenols, ascorbic acid, tocopherols, tocotrienols and carotenoids dissolved in water/methanol, water/2-propanol and 2-propanol, were tested. Our results demonstrate that the FRAP assay can quantitate satisfactorily most hydrophilic and lipophilic compounds with antioxidant properties. The reaction was followed for 60 min. The most extensive reaction occurred within the first 4 min for most compounds and foods. The lipophilic tocopherols and tocotrienols were easily quantitated and reached endpoint within 4 min while carotenoids were somewhat more demanding due to low solubility and slower reaction kinetics. We conclude that the FRAP assay, with 4 min reaction time, is suitable for high-throughput screening of total antioxidant content of edible items. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:761 / 768
页数:8
相关论文
共 27 条
[1]
[Anonymous], 2003, World Health Organ Tech Rep Ser, V916, pi
[2]
Total antioxidant capacity of teas by the ferric reducing/antioxidant power assay [J].
Benzie, IFF ;
Szeto, YT .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1999, 47 (02) :633-636
[3]
The ferric reducing ability of plasma (FRAP) as a measure of ''antioxidant power'': The FRAP assay [J].
Benzie, IFF ;
Strain, JJ .
ANALYTICAL BIOCHEMISTRY, 1996, 239 (01) :70-76
[4]
AUTOXIDATION OF BIOLOGICAL MOLECULES .1. THE ANTIOXIDANT ACTIVITY OF VITAMIN-E AND RELATED CHAIN-BREAKING PHENOLIC ANTIOXIDANTS INVITRO [J].
BURTON, GW ;
INGOLD, KU .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (21) :6472-6477
[5]
OXYGEN-RADICAL ABSORBENCY CAPACITY ASSAY FOR ANTIOXIDANTS [J].
CAO, GH ;
ALESSIO, HM ;
CUTLER, RG .
FREE RADICAL BIOLOGY AND MEDICINE, 1993, 14 (03) :303-311
[6]
Evaluation of energy and dietary intake estimates from a food frequency questionnaire using independent energy expenditure measurement and weighed food records [J].
Carlsen, Monica H. ;
Lillegaard, Inger T. L. ;
Karlsen, Anette ;
Blomhoff, Rune ;
Drevon, Christian A. ;
Andersen, Lene F. .
NUTRITION JOURNAL, 2010, 9
[7]
Fruit and vegetable consumption and risk of coronary heart disease: A meta-analysis of cohort studies [J].
Dauchet, Luc ;
Amouyel, Philippe ;
Hercberg, Serge ;
Dallongeville, Jean .
JOURNAL OF NUTRITION, 2006, 136 (10) :2588-2593
[8]
PHYCOERYTHRIN FLUORESCENCE-BASED ASSAY FOR PEROXY-RADICALS - A SCREEN FOR BIOLOGICALLY RELEVANT PROTECTIVE AGENTS [J].
DELANGE, RJ ;
GLAZER, AN .
ANALYTICAL BIOCHEMISTRY, 1989, 177 (02) :300-306
[9]
Dragland S, 2003, J NUTR, V133, P1286
[10]
Evaluation of the antioxidant activity of flavonoids by "ferric reducing antioxidant power" assay and cyclic voltammetry [J].
Firuzi, O ;
Lacanna, A ;
Petrucci, R ;
Marrosu, G ;
Saso, L .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2005, 1721 (1-3) :174-184