Metabolism and urinary excretion kinetics of di(2-ethylhexyl) terephthalate (DEHTP) in three male volunteers after oral dosage

被引:0
作者
Frederik Lessmann
André Schütze
Tobias Weiss
Angelika Langsch
Rainer Otter
Thomas Brüning
Holger M. Koch
机构
[1] Institute of the Ruhr-Universität Bochum (IPA),Institute for Prevention and Occupational Medicine of the German Social Accident Insurance
[2] BASF SE,undefined
来源
Archives of Toxicology | 2016年 / 90卷
关键词
Di(2-ethylhexyl) terephthalate; DEHTP; Plasticizer; Metabolism; Oral dosage; Human biomonitoring;
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摘要
Di(2-ethylhexyl) terephthalate (DEHTP) is used as a substitute for di(2-ethylhexyl) phthalate (DEHP), an ortho-phthalate-based plasticizer that is classified and labeled due to its toxicity to reproduction. In this study the metabolism and urinary excretion kinetics of DEHTP were investigated by single oral dosage of 50 mg DEHTP to three male volunteers (resulting in individual dosages between 0.55 and 0.59 mg/kg body weight). Separate urine samples were consecutively collected for 48 h. In analogy to DEHP, we quantified specific side-chain-oxidized monoester metabolites of DEHTP (5OH-MEHTP, 5oxo-MEHTP, 5cx-MEPTP and 2cx-MMHTP) by HPLC–MS/MS with online sample clean-up and isotope dilution. All postulated metabolites were detectable in all samples after dosage. The predominant, specific urinary metabolite was 5cx-MEPTP representing about 13.0 % of the applied dose as mean of the three volunteers (range 7.0–20.4 %) in urine, followed by 5OH-MEHTP (mean: 1.8 %; range 1.3–2.4 %) and 5oxo MEHTP (mean: 1.0 %; range 0.6–1.6 %). 2cx-MMHTP was a minor metabolite representing only 0.3 % (range 0.2–0.4 %). In total, about 16.1 % of the dose was recovered in urine as the above investigated specific metabolites within 48 h with the major share (95 %) being excreted within the first 24 h. Investigation of the glucuronidation patterns revealed that the carboxy-metabolites are excreted almost completely in their free form (>90 %), whereas for 5OH-MEHTP and 5oxo-MEHTP, glucuronidation is preferred (>70 %). With this study we provide reliable urinary excretion factors to calculate DEHTP intakes based on metabolite concentrations in environmental and occupational studies.
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页码:1659 / 1667
页数:8
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[1]  
Anderson WAC(2011)A twenty-volunteer study using deuterium labelling to determine the kinetics and fractional axcretion of primary and secondary urinary metabolites of di-2-ethylhexylphthtalate and di-iso-nonylphthalate Food Chem Toxicol 49 2022-2029
[2]  
Castle L(1956)The enzymatic cleavage of aromatic ethers Biochem J 63 634-639
[3]  
Hird S(1995)Subchronic 90-day oral toxicology of di(2-ethylhexyl) terephthalate in the rat Fd Chem Toxic 33 971-978
[4]  
Jeffery J(1994)Hydrolysis, absorption and metabolism of di(2-ethylhexy1) terephthalate in the rat Xenobiotica 24 441-450
[5]  
Scotter MJ(2011)Reproductive and behavioral effects of diisononyl phthalate (DINP) in perinatally exposed rats Reprod Toxicol 31 200-209
[6]  
Axelrod J(2016)Human exposure, hazard and risk of alternative plasticizers to phthalate esters Sci Total Environ 541 451-467
[7]  
Barber ED(2007)Carcinogenicity and chronic toxicity of di-2-ethylheyl terephthalate (DEHT) following a 2-year dietary exposure in Fischer 344 rats Food Chem Toxicol 46 990-1005
[8]  
Topping DC(2005)Opinion of the scientific panel on food additives, flavourings, processing aids and materials in contact with food (AFC) on a request from the Commission related to Bis(2-ethylhexyl)phthalate (DEHP) for use in food contact materials Question No EFSA-Q-2003-191, Adopted on 23 June 2005 by written procedure EFSA J 243 1-20
[9]  
Barber ED(2008)Opinion of the scientific panel on food additives, flavourings, processing aids and materials in contact with food (AFC) on a request related to a 18th list of substances for food contact materials. Question No EFSA-Q-2007-167, EFSA-Q-2006-177, EFSA-Q-2005-152, EFSA-Q-2007-022, EFSA-Q-2007-004, EFSA-Q-2007-024 EFSA J 628–633 1-19
[10]  
Fox JA(2006)Disruption of reproductive development in male rat offspring following in utero exposure to phthalate esters Int J Androl 29 140-147