Evaluation of reduced toxicity of zearalenone by extrusion processing as measured by the MTT cell proliferation assay

被引:45
作者
Cetin, Y [1 ]
Bullerman, LB [1 ]
机构
[1] Univ Nebraska, Dept Food Sci & Technol, Lincoln, NE 68583 USA
关键词
zearalenone; extrusion processing; detoxification; MTT bioassay; MCF-7 cell line;
D O I
10.1021/jf051120z
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The objective of this study was to determine loss of toxicity of zearalenone in extruded cereal-based products by the MTT (tetrazolium salt) cell proliferation assay using a sensitive MCF-7 human breast cancer cell line and to compare the results to chemical (high-performance liquid chromatography, HPLC) and biochemical (enzyme-linked immunosorbent assay, ELISA) methods of analysis, A split-split plot design was used for the extrusion process experiments at temperatures of 150, 175, and 200 degrees C and screw speeds of 70 and 140 rpm. The initial zearalenone concentration in the artificially contaminated corn grits with Fusarium graminearum was found at a mean concentration of 37.88 mu g/g as measured by HPLC. The percent reductions of zearalenone in the contaminated corn grits upon extrusion processing were in the ranges of 67-81, 60-72, and 66-78% as measured by HPLC, ELISA, and the MTT cell proliferation assay, respectively. The MTT cell proliferation assay results were more closely correlated with HPLC results (r = 0.96) than ELISA results (r = 0,83). The MTT cell proliferation assay was demonstrated to be a useful method for quantification of zearalenone as well as a potential toxicity screening method for contaminated extruded cereal-based products.
引用
收藏
页码:6558 / 6563
页数:6
相关论文
共 45 条
[1]   CYTOTOXICITY OF FUSARIUM SPECIES MYCOTOXINS AND CULTURE FILTRATES OF FUSARIUM SPECIES ISOLATED FROM THE MEDICINAL PLANT TRIBULUS-TERRESTRIS TO MAMMALIAN-CELLS [J].
ABEYWICKRAMA, K ;
BEAN, GA .
MYCOPATHOLOGIA, 1992, 120 (03) :189-193
[2]  
Ahamed S, 2001, MOL CARCINOGEN, V30, P88, DOI 10.1002/1098-2744(200102)30:2&lt
[3]  
88::AID-MC1017&gt
[4]  
3.0.CO
[5]  
2-E
[6]  
Aziz NH, 1997, NAHRUNG, V41, P34, DOI 10.1002/food.19970410109
[7]   Quantification of deoxynivalenol in wheat using an immunoaffinity column and liquid chromatography [J].
Cahill, LM ;
Kruger, SC ;
McAlice, BT ;
Ramsey, CS ;
Prioli, R ;
Kohn, B .
JOURNAL OF CHROMATOGRAPHY A, 1999, 859 (01) :23-28
[8]   Fate of mycotoxins in cereals during extrusion cooking:: A review [J].
Castells, M ;
Marín, S ;
Sanchis, V ;
Ramos, AJ .
FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT, 2005, 22 (02) :150-157
[9]  
Cazzaniga D, 2001, LETT APPL MICROBIOL, V33, P144, DOI 10.1046/j.1472-765X.2001.00968.x
[10]   Cytotoxicity of Fusarium mycotoxins to mammalian cell cultures as determined by the MTT bioassay [J].
Cetin, Y ;
Bullerman, LB .
FOOD AND CHEMICAL TOXICOLOGY, 2005, 43 (05) :755-764