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儿童在居住环境中接触毒死蜱的情况:在MENTOR/SHEDS-农药模型中应用毒死蜱和TCPy的CPPAES现场测量数据

Children's residential exposure to chlorpyrifos: application of CPPAES field measurements of chlorpyrifos and TCPy within MENTOR/SHEDS-Pesticides model.

作者信息

Hore Paromita, Zartarian Valerie, Xue Jianping, Ozkaynak Halûk, Wang Sheng-Wei, Yang Yu-Ching, Chu Pei-Ling, Sheldon Linda, Robson Mark, Needham Larry, Barr Dana, Freeman Natalie, Georgopoulos Panos, Lioy Paul J

机构信息

Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, NJ 08855, USA.

出版信息

Sci Total Environ. 2006 Aug 1;366(2-3):525-37. doi: 10.1016/j.scitotenv.2005.10.012. Epub 2005 Dec 19.

Abstract

The comprehensive individual field-measurements on non-dietary exposure collected in the Children's-Post-Pesticide-Application-Exposure-Study (CPPAES) were used within MENTOR/SHEDS-Pesticides, a physically based stochastic human exposure and dose model. In this application, however, the model was run deterministically. The MENTOR/SHEDS-Pesticides employed the CPPAES as input variables to simulate the exposure and the dose profiles for seven children over a 2-week post-application period following a routine residential and professional indoor crack-and-crevice chlorpyrifos application. The input variables were obtained from a personal activity diary, microenvironmental measurements and personal biomonitoring data obtained from CPPAES samples collected from the individual children and in their homes. Simulation results were compared with CPPAES field measured values obtained from the children's homes to assess the utility of the different microenvironmental data collected in CPPAES, i.e. indicator toys and wipe samplers to estimate aggregate exposures that can be result from one or more exposure pathways and routes. The final analyses of the database involved comparisons of the actual data obtained from the individual biomarker samples of a urinary metabolite of chlorpyrifos (TCPy) and the values predicted by MENTOR/SHEDS-Pesticides using the CPPAES-derived variables. Because duplicate diet samples were not part of the CPPAES study design, SHEDs-Pesticides simulated dose profiles did not account for the dietary route. The research provided more confidence in the types of data that can be used in the inhalation and dermal contact modules of MENTOR/SHEDS-Pesticides to predict the pesticide dose received by a child. It was determined that we still need additional understanding about: (1) the types of activities and durations of activities that result in non-dietary ingestion of pesticides and (2) the influence of dietary exposures on the levels of TCPy found in the urine.

摘要

儿童农药施用后暴露研究(CPPAES)中收集的非饮食暴露综合个体现场测量数据,被用于基于物理的随机人体暴露和剂量模型MENTOR/SHEDS - 农药模型中。然而,在此次应用中,该模型是确定性运行的。MENTOR/SHEDS - 农药模型将CPPAES作为输入变量,以模拟7名儿童在常规住宅和专业室内缝隙施用毒死蜱后2周内的暴露和剂量分布情况。输入变量来自个人活动日记、微环境测量以及从个体儿童及其家中采集的CPPAES样本获得的个人生物监测数据。将模拟结果与从儿童家中获得的CPPAES现场测量值进行比较,以评估CPPAES中收集的不同微环境数据的效用,即指示玩具和擦拭采样器,用于估计由一种或多种暴露途径和路线可能导致的总暴露量。数据库的最终分析涉及比较从毒死蜱尿代谢物(TCPy)的个体生物标志物样本获得的实际数据以及MENTOR/SHEDS - 农药模型使用CPPAES衍生变量预测的值。由于重复饮食样本不是CPPAES研究设计的一部分,SHEDs - 农药模型模拟剂量分布未考虑饮食途径。该研究为MENTOR/SHEDS - 农药模型的吸入和皮肤接触模块中可用于预测儿童农药剂量的数据类型提供了更多信心。研究确定,我们仍需要进一步了解:(1)导致非饮食摄入农药的活动类型和活动持续时间,以及(2)饮食暴露对尿液中TCPy水平的影响。

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