Risks for human health related to the presence of 3- and 2-monochloropropanediol (MCPD), and their fatty acid esters, and glycidyl fatty acid esters in food

被引:225
作者
Alexander, Jan
Contam, Efsa Panel Contaminants Food Chain
Barregard, Lars
Bignami, Margherita
Ceccatelli, Sandra
Cottrill, Bruce
Dinovi, Michael
Edler, Lutz
Grasl-Kraupp, Bettina
Hogstrand, Christer
Hoogenboom, Laurentius
Knutsen, Helle Katrine
Nebbia, Carlo Stefano
Oswald, Isabelle
Petersen, Annette
Rogiers, Vera Maria
Rose, Martin
Roudot, Alain-Claude
Schwerdtle, Tanja
Vleminckx, Christiane
Vollmer, Gunter
Wallace, Heather
机构
关键词
MCPD; glycidol; glycidyl fatty acid esters; process contaminant; refined oil fat;
D O I
10.2903/j.efsa.2016.4426
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
EFSA was asked to deliver a scientific opinion on free and esterified 3- and 2-monochloropropane-1, 2-diol (MCPD) and glycidyl esters in food. Esters of 3- and 2-MCPD and glycidol are contaminants of processed vegetable oils; free MCPDs are formed in some processed foods. The Panel on Contaminants in the Food Chain (CONTAM Panel) evaluated 7,175 occurrence data. Esters of 3-and 2-MCPD and glycidyl esters were found at the highest levels in palm oil/fat, but most vegetable oil/fats contain substantial quantities. Mean middle bound (MB) dietary exposure values to total 3-MCPD, 2-MCPD and glycidol, respectively, across surveys and age groups in mu g/kg body weight (bw) per day were 0.2-1.5, 0.1-0.7 and 0.1-0.9; high exposure (P95) values were 0.3-2.6, 0.2-1.2 and 0.2-2.1. Animal studies show extensive hydrolysis of esterified 3-MCPD and glycidol following oral administration; esterified and free forms were assumed to contribute equally to internal exposures. Nephrotoxicity was consistently observed in rats treated with 3-MCPD. Data on 2-MCPD toxicity were insufficient for dose-response assessments. Chronic treatment with glycidol increased the incidence of tumours in several tissues of rats and mice, likely via a genotoxic mode of action. The Panel selected a BMDL10 value for 3-MCPD of 0.077 mg/kg bw per day for induction of renal tubular hyperplasia in rats and derived a tolerable daily intake (TDI) of 0.8 mu g/kg bw per day. The mean exposure to 3-MCPD was above the TDI for 'Infants', 'Toddlers' and 'Other children'. For glycidol, the Panel selected a T25 value of 10.2 mg/kg bw per day for neoplastic effects in rats. The margins of exposure (MoEs) were 11,300-102,000 and 4,900-51,000 across surveys and age groups at mean and P95 exposures, respectively. An exposure scenario for infants receiving formula only resulted in MoEs of 5,500 (mean) and 2,100 (P95). MoEs of 25,000 or higher were considered of low health concern. (C) 2016 European Food Safety Authority. EFSA Journal published by John Wiley and Sons Ltd on behalf of European Food Safety Authority.
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页数:159
相关论文
共 274 条
[1]   Relative oral bioavailability of 3-MCPD from 3-MCPD fatty acid esters in rats [J].
Abraham, Klaus ;
Appel, Klaus E. ;
Berger-Preiss, Edith ;
Apel, Elisabeth ;
Gerling, Susanne ;
Mielke, Hans ;
Creutzenberg, Otto ;
Lampen, Alfonso .
ARCHIVES OF TOXICOLOGY, 2013, 87 (04) :649-659
[2]   Rapid and simple determination of chloropropanols (3-MCPD and 1,3-DCP) in food products using isotope dilution GC-MS [J].
Abu-El-Haj, Sameer ;
Bogusz, Maciej J. ;
Ibrahim, Zuhoor ;
Hassan, Huda ;
Al Tufail, Mohammed .
FOOD CONTROL, 2007, 18 (01) :81-90
[3]   Gene expression profile of brain regions reflecting aberrations in nervous system development targeting the process of neurite extension of rat offspring exposed developmentally to glycidol [J].
Akane, Hirotoshi ;
Saito, Fumiyo ;
Shiraki, Ayako ;
Imatanaka, Nobuya ;
Akahori, Yumi ;
Itahashi, Megu ;
Wang, Liyun ;
Shibutani, Makoto .
JOURNAL OF APPLIED TOXICOLOGY, 2014, 34 (12) :1389-1399
[4]   Downregulation of immediate-early genes linking to suppression of neuronal plasticity in rats after 28-day exposure to glycidol [J].
Akane, Hirotoshi ;
Saito, Fumiyo ;
Shiraki, Ayako ;
Takeyoshi, Masahiro ;
Imatanaka, Nobuya ;
Itahashi, Megu ;
Murakami, Tomoaki ;
Shibutani, Makoto .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2014, 279 (02) :150-162
[5]   Glycidol induces axonopathy and aberrations of hippocampal neurogenesis affecting late-stage differentiation by exposure to rats in a framework of 28-day toxicity study [J].
Akane, Hirotoshi ;
Shiraki, Ayako ;
Imatanaka, Nobuya ;
Akahori, Yumi ;
Itahashi, Megu ;
Abe, Hajime ;
Shibutani, Makoto .
TOXICOLOGY LETTERS, 2014, 224 (03) :424-432
[6]   Glycidol Induces Axonopathy by Adult-Stage Exposure and Aberration of Hippocampal Neurogenesis Affecting Late-Stage Differentiation by Developmental Exposure in Rats [J].
Akane, Hirotoshi ;
Shiraki, Ayako ;
Imatanaka, Nobuya ;
Akahori, Yumi ;
Itahashi, Megu ;
Ohishi, Takumi ;
Mitsumori, Kunitoshi ;
Shibutani, Makoto .
TOXICOLOGICAL SCIENCES, 2013, 134 (01) :140-154
[7]  
ALDEN C L, 1991, P315
[8]  
AMADOR A, 1985, J ANDROL, V6, P61
[9]   Toxicology, occurrence and risk characterisation of the chloropropanols in food: 2-Monochloro-1,3-propanediol, 1,3-dichloro-2-propanol and 2,3-dichloro-1-propanol [J].
Andres, Susanne ;
Appel, Klaus E. ;
Lampen, Alfonso .
FOOD AND CHEMICAL TOXICOLOGY, 2013, 58 :467-478
[10]   Human biomonitoring: State of the art [J].
Angerer, Juergen ;
Ewers, Ulrich ;
Wilhelm, Michael .
INTERNATIONAL JOURNAL OF HYGIENE AND ENVIRONMENTAL HEALTH, 2007, 210 (3-4) :201-228