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Estimation of Tetrabromobisphenol A (TBBPA) percutaneous uptake in humans using the parallelogram method

机译:使用平行四边形方法估算人体中四溴双酚A(TBBPA)的经皮摄取

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摘要

Tetrabromobisphenol A (TBBPA) is currently the world’s highest production volume brominated flame retardant. Humans are frequently exposed to TBBPA by the dermal route. In the present study, a parallelogram approach was used to make predictions of internal dose in exposed humans. Human and rat skin samples received 100 nmol of TBBPA/cm2 skin and absorption and penetrance were determined using a flow-through in vitro system. TBBPA-derived [14C]-radioactivity was determined at 6 hour intervals in the media and at 24 hours post-dosing in the skin. The human skin and media contained an average of 3.4% and 0.2% of the total dose at the terminal time point, respectively, while the rat skin and media contained 9.3% and 3.5%, respectively. In the intact rat, 14% of a dermally-administered dose of ~100 nmol/cm2 remained in the skin at the dosing site, with an additional 8% reaching systemic circulation by 24 hours post-dosing. Relative absorption and penetrance was less (10% total) at 24 hours following dermal administration of a ten-fold higher dose (~1,000 nmol/cm2) to rats. However, by 72 hours, 70% of this dose was either absorbed into the dosing-site skin or had reached systemic circulation. It is clear from these results that TBBPA can be absorbed by the skin and dermal contact with TBBPA may represent a small but important route of exposure. Together, these in vitro data in human and rat skin and in vivo data from rats may be used to predict TBBPA absorption in humans following dermal exposure. Based on this parallelogram calculation, up to 6% of dermally applied TBBPA may be bioavailable to humans exposed to TBBPA.
机译:四溴双酚A(TBBPA)是目前世界上产量最高的溴化阻燃剂。人类经常通过皮肤途径接触TBBPA。在本研究中,使用平行四边形方法来预测暴露人群的内部剂量。人和大鼠皮肤样品接受100 nmol的TBBPA / cm 2 皮肤,并使用流通式体外系统测定吸收和渗透率。在培养基中每隔6小时和给药后24小时测定TBBPA衍生的[ 14 C]放射性。最终时间点,人的皮肤和培养基平均分别占总剂量的3.4%和0.2%,而大鼠的皮肤和培养基分别分别占9.3%和3.5%。在完整大鼠中,约100 nmol / cm 2 的皮肤给药剂量中有14%残留在给药部位的皮肤中,另外8%给药后24小时达到全身循环。对大鼠皮下注射高剂量10倍(〜1,000 nmol / cm 2 )后24小时,相对吸收和渗透率降低(总计10%)。但是,到72小时时,该剂量的70%被吸收到给药部位的皮肤中或已经达到全身循环。从这些结果可以明显看出,TBBPA可以被皮肤吸收,而与TBBPA的皮肤接触可能代表一种小的但重要的接触途径。这些人类和大鼠皮肤的体外数据以及来自大鼠的体内数据一起,可用于预测皮肤接触后人体中的TBBPA吸收。根据此平行四边形计算,暴露于TBBPA的人类可能有高达6%的经皮肤应用的TBBPA生物利用度。

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