Silva Manori J, Hilton Donald, Furr Johnathan, Gray L Earl, Preau James L, Calafat Antonia M, Ye Xiaoyun
Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA, 30341, USA.
Reproductive Toxicology Branch, Toxicity Assessment Division, National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, NC, 27709, USA.
Arch Toxicol. 2016 Mar;90(3):551-7. doi: 10.1007/s00204-015-1489-6. Epub 2015 Mar 25.
The first withdrawal of certain polybrominated diphenyl ethers flame retardants from the US market occurred in 2004. Since then, use of brominated non-PBDE compounds such as bis(2-ethylhexyl)-2,3,4,5-tetrabromophthalate (BEH-TEBP) and 2-ethylhexyl-2,3,4,5-tetrabromobenzoate (EH-TBB) in commercial formulations has increased. Assessing human exposure to these chemicals requires identifying metabolites that can potentially serve as their biomarkers of exposure. We administered by gavage a dose of 500 mg/Kg bw of Uniplex FRP-45 (>95 % BEH-TEBP) to nine adult female Sprague-Dawley rats. Using authentic standards and mass spectrometry, we positively identified and quantified 2,3,4,5-tetrabromo benzoic acid (TBBA) and 2,3,4,5-tetrabromo phthalic acid (TBPA) in 24-h urine samples collected 1 day after dosing the rats and in serum at necropsy, 2 days post-exposure. Interestingly, TBBA and TBPA concentrations correlated well (R (2) = 0.92). The levels of TBBA, a known metabolite of EH-TBB, were much higher than the levels of TBPA both in urine and serum. Because Uniplex FRP-45 was technical grade and EH-TBB was present in the formulation, TBBA likely resulted from the metabolism of EH-TBB. Taken together, our data suggest that TBBA and TBPA may serve as biomarkers of exposure to non-PBDE brominated flame retardant mixtures. Additional research can provide useful information to better understand the composition and in vivo toxicokinetics of these commercial mixtures.
某些多溴二苯醚阻燃剂于2004年首次从美国市场撤出。自那时以来,商业配方中双(2-乙基己基)-2,3,4,5-四溴邻苯二甲酸酯(BEH-TEBP)和2-乙基己基-2,3,4,5-四溴苯甲酸酯(EH-TBB)等溴化非多溴二苯醚化合物的使用有所增加。评估人体对这些化学物质的接触情况需要识别可能作为其接触生物标志物 的代谢物。我们通过灌胃给9只成年雌性斯普拉格-道利大鼠施用了500 mg/Kg体重的Uniplex FRP-45(>95% BEH-TEBP)。使用标准品和质谱法,我们在给大鼠给药1天后收集的24小时尿液样本以及暴露后2天尸检时采集的血清中,阳性鉴定并定量了2,3,4,5-四溴苯甲酸(TBBA)和2,3,4,5-四溴邻苯二甲酸(TBPA)。有趣的是,TBBA和TBPA浓度相关性良好(R (2) = 0.92)。TBBA是EH-TBB的已知代谢物,其在尿液和血清中的水平均远高于TBPA。由于Uniplex FRP-45是工业级的且配方中存在EH-TBB,TBBA可能是由EH-TBB的代谢产生的。综上所述,我们的数据表明TBBA和TBPA可能作为接触非多溴二苯醚溴化阻燃剂混合物的生物标志物。进一步的研究可以提供有用信息,以更好地了解这些商业混合物的组成和体内毒代动力学。