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建立和应用简单药代动力学模型研究人体对邻苯二甲酸二丁酯(DnBP)和邻苯二甲酸二异丁酯(DiBP)的暴露情况。

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

机构信息

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

出版信息

Environ Int. 2013 Sep;59:469-77. doi: 10.1016/j.envint.2013.07.010. Epub 2013 Aug 15.

Abstract

In a published controlled dosing experiment, a single individual consumed 5mg each of labeled di-n-butyl phthalate (DnBP) and diisobutyl phthalate (DiBP) on separate occasions and tracked metabolites in his blood and urine over 48h. 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 0.5μg/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.

摘要

在一项已发表的受控剂量实验中,一名个体在不同时间分别摄入了 5mg 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 小时内跟踪其血液和尿液中的代谢物。这项研究的数据被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,这些模型可以预测在给定的邻苯二甲酸酯摄入情况下(时间和数量)尿液和血液代谢物的浓度。校准后的模型被应用于第二项已发表的实验中,该实验中 5 名个体在为期 48 小时的周末期间禁食(只饮用瓶装水),并收集和测量他们的全部尿液以检测 DnBP 和 DiBP 的代谢物。该模型应用的一个目标是验证校准模型的有效性——如果可以找到一种能够充分复制尿液中测量到的代谢物浓度的摄入量情况,那么模型的有效性就可以得到证明。另一个目标是研究该组的暴露模式。研究发现,所有代谢物都可以通过个体特定的“最佳拟合”摄入情况很好地复制,只有一个例外。模型预测的代谢物 3-羧基-单丙基邻苯二甲酸酯(MCPP)的浓度明显低于所有个体的观察值。作为 DnBP 的代谢物,这表明 DnBP 不是尿液中 MCPP 的主要来源。对于所有 5 名个体,两种邻苯二甲酸酯的重建剂量谱相似:每天约 6 个小剂量,摄入量约为 0.5μg/kg-day。这些摄入量似乎与参与者日记中报告的活动(个人卫生和药物使用)无关。模型频繁摄入表明存在以下两种可能性之一:持续暴露,如吸入暴露,或没有暴露,但过去暴露导致的体内邻苯二甲酸酯代谢物持续释放。

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