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Disposition of the emerging brominated flame retardant bis(2-ethylhexyl) tetrabromophthalate in female Sprague Dawley rats: effects of dose route and repeated administration

机译:在雌性Sprague Dawley大鼠中处置新兴的溴化阻燃剂双(2-乙基己基)四溴邻苯二甲酸酯:剂量途径和重复给药的影响

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class="enumerated" style="list-style-type:decimal" id="L1">Bis(2-ethylhexyl)-tetrabromophthalate (BEH-TEBP; CAS No. 26040-51-7; PubChem CID: 117291; MW 706.15 g/mol, elsewhere: TeBrDEPH, TBPH, or BEHTBP) is used as an additive brominated flame retardant in consumer products.Female Sprague Dawley rats eliminated 92–98% of [14C]-BEH-TEBP unchanged in feces after oral administration (0.1 or 10 μmol/kg). A minor amount of each dose (0.8–1%) was found in urine over 72 h. Disposition of orally administered BEH-TEBP in male B6C3F1/Tac mice was similar to female rats.Bioaccumulation of [14C]-radioactivity was observed in liver and adrenals following 10 daily oral administrations (0.1 μmol/kg/day). These tissues contained 5- and 10-fold higher concentrations of [14C]-radioactivity, respectively, versus a single dose.IV-administered [14C]-BEH-TEBP (0.1 μmol/kg) was slowly eliminated in feces, with >15% retained in tissues after 72 h. Bile and fecal extracts from these rats contained the metabolite mono-ethylhexyl tetrabromophthalate (TBMEHP).BEH-TEBP was poorly absorbed, minimally metabolized, and eliminated mostly by the fecal route after oral administration. Repeated exposure to BEH-TEBP led to accumulation in some tissues. The toxicological significance of this effect remains to be determined. This work was supported by the Intramural Research Program of the National Cancer Institute at the National Institutes of Health (Project ZIA BC 011476).
机译:class =“ enumerated” style =“ list-style-type:decimal” id =“ L1”> <!-list-behavior =枚举前缀word = mark-type = decimal max-label-size = 0- -> li(双(2-乙基己基)-四溴邻苯二甲酸酯(BEH-TEBP; CAS No.26040-51-7; PubChem CID:117291; MW 706.15 g / mol,其他:TeBrDEPH,TBPH或BEHTBP)消费品中的一种添加剂溴化阻燃剂。 Sprague Dawley雌性大鼠口服后排泄的粪便中92.98%的[ 14 C] -BEH-TEBP保持不变(0.1或0.1 10μmol/ kg)。在72小时内尿液中发现了少量的每种剂量(0.8–1%)。雄性B6C3F1 / Tac小鼠口服BEH-TEBP的处置与雌性大鼠相似。 观察每天10次肝脏和肾上腺中[ 14 C]放射性的生物蓄积口服(0.1μmol/ kg /天)。与单剂量相比,这些组织的[ 14 C]放射性浓度分别高5到10倍。 IV施用的[ 14 C] -BEH-TEBP(0.1μmol/ kg)在粪便中缓慢清除,72小时后保留在组织中的比例> 15%。这些大鼠的胆汁和粪便提取物含有四溴邻苯二甲酸单乙基己基酯(TBMEHP)代谢物。 BEH-TEBP吸收不良,代谢极少,并且在口服后大部分通过粪便途径被清除。反复暴露于BEH-TEBP会导致某些组织中积累。这种作用的毒理学意义尚待确定。这项工作得到了美国国立卫生研究院国家癌症研究所的壁内研究计划的支持(ZIA BC 011476项目)。

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