Knudsen Gabriel A, Hughes Michael F, Sanders J Michael, Hall Samantha M, Birnbaum Linda S
NCI Laboratory of Toxicology and Toxicokinetics, 111 T W Alexander Dr., Research Triangle Park, NC, USA.
Integrated Systems Toxicology Division, National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, NC 27711, USA.
Toxicol Appl Pharmacol. 2016 Nov 15;311:117-127. doi: 10.1016/j.taap.2016.10.005. Epub 2016 Oct 11.
2-Ethylhexyl-2,3,4,5-tetrabromobenzoate (EH-TBB) and bis(2-ethylhexyl)tetrabromophthalate (BEH-TEBP) are novel brominated flame retardants used in consumer products. A parallelogram approach was used to predict human dermal absorption and flux for EH-TBB and BEH-TEBP. [C]-EH-TBB or [C]-BEH-TEBP was applied to human or rat skin at 100nmol/cm using a flow-through system. Intact rats received analogous dermal doses. Treated skin was washed and tape-stripped to remove "unabsorbed" [C]-radioactivity after continuous exposure (24h). "Absorbed" was quantified using dermally retained [C]-radioactivity; "penetrated" was calculated based on [C]-radioactivity in media (in vitro) or excreta+tissues (in vivo). Human skin absorbed EH-TBB (24±1%) while 0.2±0.1% penetrated skin. Rat skin absorbed more (51±10%) and was more permeable (2±0.5%) to EH-TBB in vitro; maximal EH-TBB flux was 11±7 and 102±24pmol-eq/cm/h for human and rat skin, respectively. In vivo, 27±5% was absorbed and 13% reached systemic circulation after 24h (maximum flux was 464±65pmol-eq/cm/h). BEH-TEBP in vitro penetrance was minimal (<0.01%) for rat or human skin. BEH-TEBP absorption was 12±11% for human skin and 41±3% for rat skin. In vivo, total absorption was 27±9%; 1.2% reached systemic circulation. In vitro maximal BEH-TEBP flux was 0.3±0.2 and 1±0.3pmol-eq/cm/h for human and rat skin; in vivo maximum flux for rat skin was 16±7pmol-eq/cm/h. EH-TBB was metabolized in rat and human skin to tetrabromobenzoic acid. BEH-TEBP-derived [C]-radioactivity in the perfusion media could not be characterized. <1% of the dose of EH-TBB and BEH-TEHP is estimated to reach the systemic circulation following human dermal exposure under the conditions tested.
2-Ethylhexyl 2,3,4,5-tetrabromobenzoate (PubChem CID: 71316600; CAS No. 183658-27-7 FW: 549.92g/mol logP: 7.73-8.75 (12)) Abdallah et al., 2015a. Other published abbreviations for 2-ethylhexyl-2,3,4,5-tetrabromobenzoate are TBB EHTeBB or EHTBB Abdallah and Harrad, 2011. bis(2-ethylhexyl) tetrabromophthalate (PubChem CID: 117291; CAS No. 26040-51-7 FW: 706.14g/mol logP: 9.48-11.95 (12)). Other published abbreviations for bis(2-ethylhexyl)tetrabromophthalate are TeBrDEPH TBPH or BEHTBP.
2-乙基己基-2,3,4,5-四溴苯甲酸酯(EH-TBB)和双(2-乙基己基)四溴邻苯二甲酸酯(BEH-TEBP)是用于消费品中的新型溴化阻燃剂。采用平行四边形方法预测EH-TBB和BEH-TEBP的人体皮肤吸收和通量。使用流通系统将[C]-EH-TBB或[C]-BEH-TEBP以100nmol/cm²的剂量施用于人体或大鼠皮肤。完整的大鼠接受类似的皮肤剂量。连续暴露(24小时)后,对处理过的皮肤进行清洗并胶带剥离以去除“未吸收的”[C]-放射性。通过皮肤保留的[C]-放射性对“吸收量”进行定量;“渗透量”根据培养基(体外)或排泄物+组织(体内)中的[C]-放射性计算得出。人体皮肤吸收了EH-TBB(24±1%),而0.2±0.1%渗透过皮肤。大鼠皮肤在体外吸收更多(51±10%)且对EH-TBB的渗透性更强(2±0.5%);人体和大鼠皮肤的最大EH-TBB通量分别为11±7和102±24pmol-eq/cm²/h。在体内,24小时后27±5%被吸收,13%进入体循环(最大通量为464±65pmol-eq/cm²/h)。对于大鼠或人体皮肤,BEH-TEBP在体外的渗透率极低(<0.01%)。人体皮肤对BEH-TEBP的吸收为12±11%,大鼠皮肤为41±3%。在体内,总吸收量为27±9%;1.2%进入体循环。人体和大鼠皮肤的体外最大BEH-TEBP通量分别为0.3±0.2和1±0.3pmol-eq/cm²/h;大鼠皮肤在体内的最大通量为16±7pmol-eq/cm²/h。EH-TBB在大鼠和人体皮肤中代谢为四溴苯甲酸。灌注培养基中源自BEH-TEBP的[C]-放射性无法进行表征测定。在测试条件下,估计人体皮肤暴露后,EH-TBB和BEH-TEHP剂量的<1%会进入体循环。
2-乙基己基2,3,4,5-四溴苯甲酸酯(PubChem CID:71316600;CAS编号:183658-27-7;分子量:549.92g/mol;logP:7.73 - 8.75(12))Abdallah等人,2015a。2-乙基己基-2,3,4,5-四溴苯甲酸酯的其他已发表缩写为TBB EHTeBB或EHTBB Abdallah和Harrad,2011。双(2-乙基己基)四溴邻苯二甲酸酯(PubChem CID:117291;CAS编号:26040-51-7;分子量:706.14g/mol;logP:9.48 - 11.95(12))。双(2-乙基己基)四溴邻苯二甲酸酯的其他已发表缩写为TeBrDEPH、TBPH或BEHTBP。