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Development and application of simple pharmacokinetic models to study human exposure to di-n-butyl phthalate (DnBP) and diisobutyl phthalate (DiBP)

机译:研究人体暴露于邻苯二甲酸二正丁酯(DnBP)和邻苯二甲酸二异丁酯(DiBP)的简单药代动力学模型的开发和应用

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摘要

In a published controlled dosing experiment, a single individual consumed 5 mg each of labeled di-n-butyl phthalate (DnBP) and diisobutyl phthalate (DiBP) on separate occasions and tracked metabolites in his blood and urine over 48 h. Data from this study were used to structure and calibrate simple pharmacokinetic (PK) models for these two phthalates, which predict urine and blood metabolite concentrations with a given phthalate intake scenario (times and quantities). The calibrated models were applied to a second published experiment in which 5 individuals fasted over the course of a 48-h weekend (bottled water only), and their full urine voids were captured and measured for DnBP and DiBP metabolites. One goal of this model application was to confirm the validity of the calibrated models - their validity would be demonstrated if a profile of intakes could be found which adequately duplicated the metabolite concentrations measured in the urine. A second goal was to study patterns of exposure for this group. It was found that all metabolites could be duplicated very well with individual-specific "best-fit" intake scenarios, with one exception. It appears that the model predicted much lower concentrations of the metabolite, 3carboxy-mono-propylphthalate (MCPP), than were observed in all individuals. Modeled as a metabolite of DnBP, this suggests that DnBP was not the major source of MCPP in the urine. For all 5 individuals, the reconstructed dose profiles of the two phthalates were similar: about 6 small bolus doses per day and an intake of about 0.5 μg/kg-day. The intakes did not appear to be associated with diary-reported activities (personal hygiene and medication) of the participants. The modeled frequent intakes suggested one (or both) of two possibilities: ongoing exposures such as an inhalation exposure, or no exposure but rather an ongoing release of body stores of the phthalate metabolites from past exposures.
机译:在已公布的受控剂量实验中,一个人在单独的场合分别消耗了5 mg标记的邻苯二甲酸二正丁酯(DnBP)和邻苯二甲酸二异丁酯(DiBP),并在48小时内追踪了他的血液和尿液中的代谢产物。这项研究的数据用于构建和校准这两种邻苯二甲酸酯的简单药代动力学(PK)模型,该模型可预测在给定邻苯二甲酸酯摄入情况(时间和数量)下尿液和血液代谢产物的浓度。校准后的模型用于第二次公开发表的实验,其中5个人在一个48小时的周末禁食(仅瓶装水),并捕获其全部尿液并测量DnBP和DiBP代谢产物。该模型应用程序的一个目标是确认校准模型的有效性-如果可以找到能充分复制尿液中测得的代谢物浓度的摄入量数据,便可以证明其有效性。第二个目标是研究该人群的接触方式。研究发现,除个别例外,所有代谢物都可以与特定于个体的“最适合”摄入情况很好地复制。似乎该模型预测的代谢物,即3-羧基-单-丙基邻苯二甲酸酯(MCPP)的浓度比在所有个体中观察到的浓度低得多。建模为DnBP的代谢产物,这表明DnBP不是尿中MCPP的主要来源。对于所有5个人,两种邻苯二甲酸酯的重构剂量曲线相似:每天约6次小剂量推注,每天摄入约0.5μg/ kg。摄入量似乎与参与者的日记报告的活动(个人卫生和药物治疗)无关。建模的频繁摄入建议了两种可能性中的一种(或两种):持续暴露,例如吸入暴露,或没有暴露,而是从过去的暴露中不断释放邻苯二甲酸酯代谢物的体内储存。

著录项

  • 来源
    《Environment international》 |2013年第9期|469-477|共9页
  • 作者

    Matthew Lorber; Holger M. Koch;

  • 作者单位

    Office of Research and Development, United States Environmental Protection Agency, 1200 Pennsylvania Ave, NW, Washington, DC 20460, United States;

    Institute for Prevention and Occupational Medicine of the German Social Accident Insurance - Institute of the Ruhr-Universitat Bochum (IPA), Buerkle-de-la-Camp Platz 1, 44789 Bochum, Germany;

  • 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

    Phthalates; DnBP; DiBP; PK modeling; Exposure modeling;

    机译:邻苯二甲酸盐;DnBP;DiBP;PK建模;曝光建模;

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