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Bounding uncertainties in intrinsic human elimination half-lives and intake of polybrominated diphenyl ethers in the North American population

机译:北美人口中人类固有的消除半衰期和摄入多溴联苯醚的不确定性

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摘要

We examine the balance between intake, intrinsic elimination half-lives and human body burdens measured in biomonitoring for polybrominated diphenyl ethers (PBDEs) in the North American population using the population-level pharmacokinetic model developed by Ritter et al. (2011). Empirical data are collected from two studies that made total intake estimates for the North American population for the years 2004 and 2005, and eight biomonitoring studies for the years 1992 to 2009. We assume intake of PBDEs increased exponentially to a peak in 2004, and has since exponentially declined. The model is fitted to the empirical PBDE intake and biomonitoring data on PBDE body burden using a least-square optimization method by adjusting the intake in 2004 and 2038, and the intrinsic elimination rate constants, which can be expressed as equivalent half-lives. We fit the model in two types of scenarios using different combinations of PBDE intake estimates and biomonitoring data. Our modeling results indicate that there is an inconsistency between the PBDE intake estimates and the biomonitoring data, and that the inconsistency is likely due to underestimation of population-level intake. More efforts are needed to better characterize intake rates and identify potentially-unrecognized exposure pathways. Additional age-stratified biomonitoring data, and time trends of PBDE intakes would better constrain the model and provide an improved estimation of the intrinsic elimination half-lives.
机译:我们使用Ritter等人开发的人群水平药代动力学模型,检查了北美人群中多溴联苯醚(PBDEs)的生物监测中所测量的摄入量,固有消除半衰期和人体负担之间的平衡。 (2011)。从两项对2004年和2005年北美人口的总摄入量进行估算的研究以及从1992年至2009年的八项生物监测研究中收集的经验数据。我们假设PBDEs的摄入量呈指数增长,在2004年达到峰值,并且自从呈指数下降以来。通过最小二乘法优化方法,通过调整2004年和2038年的摄入量以及固有消除率常数,将该模型拟合为PBDE的经验摄入量和有关PBDE体负荷的生物监测数据,以及固有的消除率常数(可以表示为等效半衰期)。我们使用PBDE摄入量估算值和生物监测数据的不同组合将模型拟合为两种类型的情景。我们的模型结果表明,多溴二苯醚的摄入量估计数与生物监测数据之间存在不一致,并且这种不一致可能是由于对人口水平摄入量的低估所致。需要做出更大的努力来更好地表征摄入率并确定潜在的未被认可的接触途径。其他按年龄分层的生物监测数据以及多溴二苯醚摄入的时间趋势将更好地约束该模型,并提供对固有消除半衰期的改进估算。

著录项

  • 来源
    《Environment international》 |2013年第9期|168-174|共7页
  • 作者单位

    Department of Applied Environmental Science, Stockholm University, Svante Arrhenius vaeg 8, SE-10691, Stockholm, Sweden;

    Department of Applied Environmental Science, Stockholm University, Svante Arrhenius vaeg 8, SE-10691, Stockholm, Sweden;

    Department of Applied Environmental Science, Stockholm University, Svante Arrhenius vaeg 8, SE-10691, Stockholm, Sweden;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    PBDE; Exposure; Intake; Biomonitoring; Intrinsic elimination half-lives; Pharmacokinetic modeling;

    机译:PBDE;接触;录取;生物监测;本征消除半衰期;药代动力学模型;

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