Natural occurrence of bisphenol F in mustard

被引:50
作者
Zoller, Otmar [1 ]
Brueschweiler, Beat J. [1 ]
Magnin, Roxane [1 ]
Reinhard, Hans [1 ]
Rhyn, Peter [1 ]
Rupp, Heinz [1 ]
Zeltner, Silvia [1 ]
Felleisen, Richard [1 ]
机构
[1] Fed Food Safety & Vet Off FSVO, Risk Assessment Div, Bern, Switzerland
来源
FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT | 2016年 / 33卷 / 01期
关键词
Bisphenol F; bisphenols; endocrine disruptor; mustard; Sinapis alba; glucosinalbin; 4-hydroxybenzyl alcohol; 2; 4-bis(4-hydroxybenzyl)-phenol; bamboo shoots; taxiphyllin; IN-VIVO; PRODUCTS; ANALOGS; QUANTIFICATION; CHROMATOGRAPHY; ALTERNATIVES; CONSTITUENTS; FOODSTUFFS; SINALBIN; FOOD;
D O I
10.1080/19440049.2015.1110623
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Bisphenol F (BPF) was found in mustard up to a concentration of around 8mgkg(-1). Contamination of the raw products or caused by the packaging could be ruled out. Also, the fact that only the 4,4'-isomer of BPF was detected spoke against contamination from epoxy resin or other sources where technical BPF is used. Only mild mustard made of the seeds of Sinapis alba contained BPF. In all probability BPF is a reaction product from the breakdown of the glucosinolate glucosinalbin with 4-hydroxybenzyl alcohol as an important intermediate. Hot mustard made only from brown mustard seeds (Brassica juncea) or black mustard seeds (Brassica nigra) contained no BPF. BPF is structurally very similar to bisphenol A and has a similar weak estrogenic activity. The consumption of a portion of 20g of mustard can lead to an intake of 100-200 mu g of BPF. According to a preliminary risk assessment, the risk of BPF in mustard for the health of consumers is considered to be low, but available toxicological data are insufficient for a conclusive evaluation. It is a new and surprising finding that BPF is a natural food ingredient and that this is the main uptake route. This insight sheds new light on the risk linked to the family of bisphenols.
引用
收藏
页码:137 / 146
页数:10
相关论文
共 32 条
[1]   Sinapis phylogeny and evolution of glucosinolates and specific nitrile degrading enzymes [J].
Agerbirk, Niels ;
Warwick, Suzanne I. ;
Hansen, Paul R. ;
Olsen, Carl E. .
PHYTOCHEMISTRY, 2008, 69 (17) :2937-2949
[2]   Supercritical fluid chromatography as a method of analysis for the determination of 4-hydroxybenzylglucosinolate degradation products [J].
Buskov, S ;
Hasselstrom, J ;
Olsen, CE ;
Sorensen, H ;
Sorensen, JC ;
Sorensen, S .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2000, 43 (1-3) :157-174
[3]   Cytostatic and antiestrogenic effects of 2-(indol-3-ylmethyl)-3,3′-diindolylmethane, a major in vivo product of dietary indole-3-carbinol [J].
Chang, YC ;
Riby, J ;
Chang, GHF ;
Peng, BC ;
Firestone, G ;
Bjeldanes, LF .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (05) :825-834
[4]   Update on glucosinolate metabolism and transport [J].
Chen, S ;
Andreasson, E .
PLANT PHYSIOLOGY AND BIOCHEMISTRY, 2001, 39 (09) :743-758
[5]  
CVUA Stuttgart, 2015, BISPH F MUST DOES TH
[6]   STRUCTURE ELUCIDATION OF ACID REACTION-PRODUCTS OF INDOLE-3-CARBINOL - DETECTION INVIVO AND ENZYME-INDUCTION INVITRO [J].
DEKRUIF, CA ;
MARSMAN, JW ;
VENEKAMP, JC ;
FALKE, HE ;
NOORDHOEK, J ;
BLAAUBOER, BJ ;
WORTELBOER, HM .
CHEMICO-BIOLOGICAL INTERACTIONS, 1991, 80 (03) :303-315
[7]  
DODDS E. C, 1936, NATURE [LONDON], V137, P996, DOI 10.1038/137996a0
[8]  
Ebermann R, 2008, LEHRBUCH LEBENSMITTE
[10]   A new chapter in the bisphenol A story: bisphenol S and bisphenol F are not safe alternatives to this compound [J].
Eladak, Soria ;
Grisin, Tiphany ;
Moison, Delphine ;
Guerquin, Marie-Justine ;
N'Tumba-Byn, Thierry ;
Pozzi-Gaudin, Stephanie ;
Benachi, Alexandra ;
Livera, Gabriel ;
Rouiller-Fabre, Virginie ;
Habert, Rene .
FERTILITY AND STERILITY, 2015, 103 (01) :11-21