Antioxidant inhibition of oxygen radicals for measurement of total antioxidant capacity in biological samples

被引:23
作者
Ching, SYL [1 ]
Hall, J
Croft, K
Beilby, J
Rossi, E
Ghisalberti, E
机构
[1] Queen Elizabeth II Med Ctr, PathW Lab Med WA, Nedlands, WA 6009, Australia
[2] Varian Australia Pty Ltd, Belmont, WA, Australia
[3] Univ Western Australia, Sch Med & Pharmacol, Perth, WA 6009, Australia
[4] Univ Western Australia, Sch Biomed Biomol & Chem Sci, Perth, WA 6009, Australia
关键词
total antioxidant capacity; antioxidant inhibition of oxygen radicals; uroporphyrin I; fluorescence; mass spectrometry; reaction kinetic;
D O I
10.1016/j.ab.2006.02.027
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Few methods for assessing total antioxidant capacity (TAC) include both the percentage of inhibition and the length of inhibition in the measurement. Available methods require above ambient constant temperature incubation, reaction preheating. and/or separate assays for testing hydrophilic and hydrophobic samples. We describe a high-throughput method, antioxidant inhibition of oxygen radicals (AIOR). that overcomes these difficulties. AIOR uses peroxyl radicals to trigger a decrease in fluorescence of the indicator molecule. uroporphyrin I, which is delayed by the presence of antioxidants. The area under the curve is measured by a fluorescence spectrophotometer in a 96-well microplate format, and TAC results are expressed as millimole/liter Trolox equivalents. AIOR is performed at ambient temperature and is applicable to samples in either aqueous or common organic solvents. The reaction between uroporphyrin I and the peroxvl radicals generated from 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) was found to be of first-order kinetics with a mean rate constant (k) of 0.0254. Applications to measure antioxidant capacity are demonstrated on individual chemicals and biological samples. The method has good linearity, within- and between-assay precision, and recovery. Crown Copyright (c) 2006 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:257 / 265
页数:9
相关论文
共 14 条
[1]  
Alho H, 1999, METHOD ENZYMOL, V299, P3
[2]  
[Anonymous], FREE RADICALS ANTIOX
[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]  
CAO G, 1995, CLIN CHEM, V41, P1738
[5]  
Cao GH, 1998, CLIN CHEM, V44, P1309
[6]   A FLUORESCENCE-BASED METHOD FOR MEASURING TOTAL PLASMA ANTIOXIDANT CAPABILITY [J].
GHISELLI, A ;
SERAFINI, M ;
MAIANI, G ;
AZZINI, E ;
FERROLUZZI, A .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (01) :29-36
[7]  
GLAZER AN, 1990, METHOD ENZYMOL, V186, P161
[8]   High-throughput assay of oxygen radical absorbance capacity (ORAC) using a multichannel liquid handling system coupled with a microplate flourescence reader in 96-well format [J].
Huang, DJ ;
Ou, BX ;
Hampsch-Woodill, M ;
Flanagan, JA ;
Prior, RL .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2002, 50 (16) :4437-4444
[9]   Development and validation of an improved oxygen radical absorbance capacity assay using fluorescein as the fluorescent probe [J].
Ou, BX ;
Hampsch-Woodill, M ;
Prior, RL .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (10) :4619-4626
[10]  
RICEEVANS C, 1994, METHOD ENZYMOL, V234, P279