Antioxidant-capacity-based models for the prediction of acrylamide reduction by flavonoids

被引:45
作者
Cheng, Jun [1 ,2 ]
Chen, Xinyu [1 ,2 ]
Zhao, Sheng [3 ]
Zhang, Yu [1 ,2 ]
机构
[1] Zhejiang Univ, Zhejiang Key Lab Agrofood Proc, Fuli Inst Food Sci, Zhejiang R&D Ctr Food Technol & Equipment, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Coll Biosyst Engn & Food Sci, Dept Food Sci & Nutr, Hangzhou 310058, Zhejiang, Peoples R China
[3] Zhejiang Univ, Dept Control Sci & Engn, Hangzhou 310027, Zhejiang, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
Acrylamide; Reduction; Flavonoids; Predictive models; Antioxidant capacity; Microwave processing; ARTIFICIAL NEURAL-NETWORK; ASPARAGINE; EXTRACTS; POLYPHENOLS; SYSTEM; POWER; FRAP; FOOD;
D O I
10.1016/j.foodchem.2014.07.008
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The aim of this study was to investigate the applicability of artificial neural network (ANN) and multiple linear regression (MLR) models for the estimation of acrylamide reduction by flavonoids, using multiple antioxidant capacities of Maillard reaction products as variables via a microwave food processing workstation. The addition of selected flavonoids could effectively reduce acrylamide formation, which may be closely related to the number of phenolic hydroxyl groups of flavonoids (R: 0.735-0.951, P < 0.001). The rate of inhibition of acrylamide formation correlated well with the change of trolox equivalent antioxi'dant capacity (Delta TEAC) measured by DPPH (R-2 = 0.833), ABTS (R-2 = 0.860) or FRAP (R-2 = 0.824) assay. Both ANN and MLR models could effectively serve as predictive tools for estimating the reduction of acrylamide affected by flavonoids. The current predictive model study provides a low-cost and easy-to-use approach to the estimation of rates at which acrylamide is degraded, while avoiding tedious sample pretreatment procedures and advanced instrumental analysis. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:90 / 99
页数:10
相关论文
共 42 条
  • [1] The ferric reducing ability of plasma (FRAP) as a measure of ''antioxidant power'': The FRAP assay
    Benzie, IFF
    Strain, JJ
    [J]. ANALYTICAL BIOCHEMISTRY, 1996, 239 (01) : 70 - 76
  • [2] Inhibitory Mechanism of Naringenin against Carcinogenic Acrylamide Formation and Nonenzymatic Browning in Maillard Model Reactions
    Cheng, Ka-Wing
    Zeng, Xiaohui
    Tang, Yun Sang
    Wu, Jia-Jun
    Liu, Zhiwei
    Sze, Kong-Hung
    Chu, Ivan K.
    Chen, Feng
    Wang, Mingfu
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 2009, 22 (08) : 1483 - 1489
  • [3] Ciesarová Z, 2008, J FOOD NUTR RES, V47, P1
  • [4] Inhibition of key aroma compound generated during ultrahigh-temperature processing of bovine milk via epicatechin addition
    Colahan-Sederstrom, PM
    Peterson, DG
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2005, 53 (02) : 398 - 402
  • [5] UV spectrophotometry method for the monitoring of galacto-oligosaccharides production
    Dias, Luis G.
    Veloso, Ana C. A.
    Correia, Daniela M.
    Rocha, Orlando
    Torres, Duarte
    Rocha, Isabel
    Rodrigues, Ligia R.
    Peres, Antonio M.
    [J]. FOOD CHEMISTRY, 2009, 113 (01) : 246 - 252
  • [6] Fernndez S., 2003, Innovations in Food Technology, V18, P24
  • [7] Comparison of ABTS/DPPH assays to measure antioxidant capacity in popular antioxidant-rich US foods
    Floegel, Anna
    Kim, Dae-Ok
    Chung, Sang-Jin
    Koo, Sung I.
    Chun, Ock K.
    [J]. JOURNAL OF FOOD COMPOSITION AND ANALYSIS, 2011, 24 (07) : 1043 - 1048
  • [8] Frankel EN, 2000, J SCI FOOD AGR, V80, P1925, DOI 10.1002/1097-0010(200010)80:13<1925::AID-JSFA714>3.0.CO
  • [9] 2-4
  • [10] Acrylamide formation and antioxidant level in biscuits related to recipe and baking
    Haase, N. U.
    Grothe, K. -H.
    Matthaeus, B.
    Vosmann, K.
    Lindhauer, M. G.
    [J]. FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT, 2012, 29 (08): : 1230 - 1238