首页> 外文会议>Annual conference of the International Society of Exposure Science >Development and Application of Simple Pharmacokinetic Models to Study Human Exposure to Di-n-butyl phthalate (DnBP) and diisobutyl phthalate (DiBP)
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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:简单药代动力学模型研究人体暴露于邻苯二甲酸二丁酯(DNBP)和邻苯二甲酸二异丁酯(DIBP)的开发和应用

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In a 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 hours. Published data from this study was used to structure and calibrate simple pharmacokinetic (PK) models for these 2 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 experiment in which 5 individuals fasted over the course of a 48-hr 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 cohort. It was found that all metabolites could be duplicated very well with individual-specific "best-fit" intake scenarios. 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 medicine) of the participants. All reconstructed intakes of DnBP and DiBP occurred at exactly the same times, suggesting similar (if not the exact same) sources of exposure for these two phthalates. 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:在受控给药实验中,单独使用5mg的单个个体在单独的场合和邻苯二甲酸二异丁酯(DIBP)中标记的二丁酯(DNBP)和二异丁基二丁酯(DIBP),在48小时内跟踪代谢物和尿液。本研究的已发表的数据用于结构和校准这两个邻苯二甲酸盐的简单药代动力学(PK)模型,其预测尿液和血液代谢物浓度,所述邻苯二甲酸盐的摄入场景(时间和数量)。将校准模型应用于第二种实验,其中5个在48小时周末(仅限瓶装水)的过程中捕获的5个体,并捕获并测量DNBP和DIBP代谢物的完全尿液。该模型应用程序的一个目标是确认校准模型的有效性 - 如果可以发现进口的轮廓,则会证明它们的有效性将对尿液中测量的代谢物浓度充分复制。第二个目标是研究这种队列的暴露模式。发现所有代谢物都可以与个体特定的“最合适”的摄入场景非常复制。对于所有5个个体,两个邻苯二甲酸盐的重建剂量曲线类似:每天约6个小推注剂量,摄入约0.5μg/ kg。摄入量似乎没有与参与者的日记报告的活动(个人卫生和药物)有关。所有重建的DNBP和DIBP的摄入量完全相同,表明这两个邻苯二甲酸酯的暴露源相似(如果不是完全相同的)。建模的频繁摄入量建议两种可能性:持续暴露,例如吸入暴露,或者没有暴露,而是从过去的曝光中邻近邻苯二甲酸酯代谢物的身体储存的持续释放。

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