Effect of thermal processing on the flavonols rutin and quercetin

被引:357
作者
Buchner, Nadja
Krumbein, Angelika
Rohn, Sascha
Kroh, Lothar W.
机构
[1] Tech Univ Berlin, Inst Food Technol & Food Chem, Dept Food Anal, D-13355 Berlin, Germany
[2] Grossbeeren EV, Inst Vegetable & Ornamental Crops, D-14979 Grosshansdorf, Germany
关键词
D O I
10.1002/rcm.2720
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The current research involves the study of the thermal treatment of quercetin and rutin in an aqueous model system (cooking). These substances were heated and their degradation was followed by high-performance liquid chromatography/diode-array detection (HPLC/DAD). The influence of pH and the involvement of oxygen in the degradation were studied. HPLC/electrospray ionization multi-stage mass spectrometry (ESI-MSn) was used for the structural characterization of the compounds produced. The influence of the degradation of the phenolic compounds on their antioxidant properties was elucidated by a electron spin resonance (ESR) spectrometry study of the reaction samples mixed with the stabilized radical, Fremy's salt. Strong degradation of the model substances took place under weak basic and oxidative conditions. Quercetin showed the most intense degradation. Protocatechuic acid could be identified as a cleavage reaction product by analyzing its retention time and molar mass during the degradation of quercetin. The structure of a second cleavage product could be identified on the basis of ESI-MSn fragmentation data. Also, several structures for reaction products of oxidized quercetin are suggested. The ESR analysis showed a decrease in the antioxidant activity of the reaction samples after heat treatment in aqueous solution. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:3229 / 3235
页数:7
相关论文
共 19 条
[1]
Brown JE, 1998, BIOCHEM J, V330, P1173
[2]
Antioxidant and prooxidant behavior of flavonoids: Structure-activity relationships [J].
Cao, GH ;
Sofic, E ;
Prior, RL .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (05) :749-760
[3]
Quantitative analysis of the flavonoid content of commercial tomatoes, onions, lettuce, and celery [J].
Crozier, A ;
Lean, MEJ ;
McDonald, MS ;
Black, C .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (03) :590-595
[4]
Chemistry, biochemistry, and dietary role of potato polyphenols. A review [J].
Friedman, M .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (05) :1523-1540
[5]
Study of the reaction products of flavonols with 2,2-diphenyl-1-picrylhydrazyl using liquid chromatography coupled with negative electrospray ionization tandem mass spectrometry [J].
Hvattum, E ;
Stenstrom, Y ;
Ekeberg, D .
JOURNAL OF MASS SPECTROMETRY, 2004, 39 (12) :1570-1581
[6]
2,5,7,3',4'-PENTAHYDROXYFLAVAN-3,4-DIONE AS AN INTERMEDIATE PRODUCT IN THE ENZYME-CATALYZED OXIDATION OF QUERCETIN [J].
IGARASHI, K ;
KOMATSU, C ;
SHIMADA, T .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1991, 55 (03) :855-857
[7]
Flavonoid intake and risk of chronic diseases [J].
Knekt, P ;
Kumpulainen, J ;
Järvinen, R ;
Rissanen, H ;
Heliövaara, M ;
Reunanen, A ;
Hakulinen, T ;
Aromaa, A .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2002, 76 (03) :560-568
[8]
In vitro flavon-3-ol oxidation mediated by a B ring hydroxylation pattern [J].
Krishnamachari, V ;
Levine, LH ;
Zhou, C ;
Paré, PW .
CHEMICAL RESEARCH IN TOXICOLOGY, 2004, 17 (06) :795-804
[9]
Flavonoid oxidation by the radical generator AIBN:: A unified mechanism for quercetin radical scavenging [J].
Krishnamachari, V ;
Levine, LH ;
Paré, PW .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2002, 50 (15) :4357-4363
[10]
Antioxidant capacity and phenolic content in leaf extracts of tree spinach (Cnidoscolus spp.) [J].
Kuti, JO ;
Konuru, HB .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (01) :117-121