Biomonitoring Equivalents for Interpreting Mandelic and Phenylglyoxylic Acid in Urine Resulting From Exposures to Styrene and Ethylbenzene.

IF 3.5 4区 医学 Q1 MEDICINE, LEGAL
Sean M Hays, Ted W Simon, Xichen Chou, Christopher R Kirman
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Abstract

Styrene and ethylbenzene are chemicals used in the plastic and rubber industry and are present in cigarette smoke. Regulatory authorities have developed toxicological reference values to conduct risk assessments for potential exposures. The extent of exposures to ST and ETB can be assessed via biomonitoring of shared metabolites mandelic acid and phenylglyoxylic acid in urine. The metabolism of ST and ETB and the excretion of MA and PGA in urine following controlled inhalation exposures in humans has been studied. In this evaluation, we derive Biomonitoring Equivalents (BEs) for interpretation of general population biomonitoring data. BEs are defined as the concentration or range of concentrations of a chemical or its metabolite in a biological medium (blood, urine, human milk, etc.) that is consistent with existing health-based TRVs such as a reference concentration. The BE values derived in this manuscript are screening values that can help public health officials and regulators interpret biomonitoring data for styrene and ethylbenzene. Examples of interpretating existing biomonitoring data available from the National Health And Nutrition Examination Survey are provided, with additional considerations given to understanding potential sources of confounding associated with body mass index and sex.

暴露于苯乙烯和乙苯后尿液中苯乙醛酸和苯乙醛酸的生物监测等效解释。
苯乙烯和乙苯是塑料和橡胶工业中使用的化学物质,也存在于香烟烟雾中。监管当局制定了毒理学参考值,以便对潜在接触进行风险评估。暴露于ST和ETB的程度可以通过尿液中共同代谢物扁桃酸和苯乙醛酸的生物监测来评估。已经研究了控制吸入暴露后人类尿中ST和ETB的代谢以及MA和PGA的排泄。在本评估中,我们推导了生物监测当量(BEs)来解释一般人群的生物监测数据。生化指标被定义为生物介质(血液、尿液、人乳等)中某种化学品或其代谢物的浓度或浓度范围,该浓度或浓度范围与现有基于健康的trv(如参考浓度)相一致。本文中导出的BE值是筛选值,可以帮助公共卫生官员和监管机构解释苯乙烯和乙苯的生物监测数据。提供了解释国家健康和营养检查调查提供的现有生物监测数据的例子,并考虑到了解与体重指数和性别相关的混淆的潜在来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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