Wilson Nancy K, Chuang Jane C, Morgan Marsha K, Lordo Robert A, Sheldon Linda S
Battelle Memorial Institute, 100 Capitola Drive, Suite 301, Durham, NC 27713-4411, USA.
Environ Res. 2007 Jan;103(1):9-20. doi: 10.1016/j.envres.2006.04.006. Epub 2006 Jun 5.
The Children's Total Exposure to Persistent Pesticides and Other Persistent Organic Pollutants (CTEPP) study investigated the potential exposures of 257 preschool children, ages 1 1/2-5 yr, and their primary adult caregivers to more than 50 anthropogenic chemicals. Field sampling took place in selected counties in North Carolina (NC) and Ohio (OH) in 2000-2001. Over a 48-h period in each child's daycare center and/or home, food, beverages, indoor air, outdoor air, house dust, soil, participants' hand surfaces and urine were sampled. Additional samples-transferable residues, food preparation surface wipes, and hard floor surface wipes-were collected in the approximately 13% of the homes that had pesticide applications within the 7 days prior to field sampling. Three phenols were among the measured chemicals: pentachlorophenol (PCP), bisphenol-A [2,2-bis(4-hydroxyphenyl)propane], and nonylphenol (4-n-nonylphenol). Nonylphenol (NP) was detected in less than 11% of the samples in any medium. Among samples that were collected at all participants' homes and daycare centers, PCP was detected in >50% of indoor air, outdoor air, house dust, and urine samples; bisphenol-A (BPA) was detected in >50% of indoor air, hand wipe, solid food, and liquid food samples. The concentrations of the phenols in the sampled media were measured, and the children's potential exposures and potential absorbed doses resulting from intake through the inhalation, dietary ingestion, and indirect ingestion routes of exposure were estimated. The children's potential exposures to PCP were predominantly through inhalation: 78% in NC and 90% in OH. In contrast, their potential exposures to BPA were predominantly through dietary ingestion: 99%, for children in both states. The children's estimated exposures to PCP, calculated from the amounts excreted in their urine, exceeded their estimated maximum potential intake, calculated from the multimedia PCP concentrations, by a factor greater than 10. This inconsistency for PCP highlights the need for further research on the environmental pathways and routes of PCP exposure, investigation of possible exposures to other compounds that could be metabolized to PCP, and on the human absorption, metabolism, and excretion of this phenol over time periods longer than 48 h.
儿童对持久性农药和其他持久性有机污染物的总暴露量(CTEPP)研究调查了257名1.5至5岁学龄前儿童及其主要成年照料者对50多种人为化学物质的潜在暴露情况。2000 - 2001年在北卡罗来纳州(NC)和俄亥俄州(OH)的部分县进行了现场采样。在每个孩子的日托中心和/或家中,经过48小时,对食物、饮料、室内空气、室外空气、房屋灰尘、土壤、参与者的手部表面和尿液进行了采样。在现场采样前7天内有农药施用的约13%的家庭中,还采集了额外的样本——可转移残留物、食品制备表面擦拭物和硬地板表面擦拭物。所测化学物质中有三种酚类:五氯酚(PCP)、双酚A [2,2 - 双(4 - 羟基苯基)丙烷]和壬基酚(4 - 正壬基酚)。在任何介质中,壬基酚(NP)在不到11%的样本中被检测到。在所有参与者的家中和日托中心采集的样本中,PCP在超过50%的室内空气、室外空气、房屋灰尘和尿液样本中被检测到;双酚A(BPA)在超过50%的室内空气、手部擦拭物、固体食物和液体食物样本中被检测到。测量了采样介质中酚类的浓度,并估算了儿童通过吸入、饮食摄入和间接摄入暴露途径摄入后产生的潜在暴露量和潜在吸收剂量。儿童对PCP的潜在暴露主要通过吸入:北卡罗来纳州为78%,俄亥俄州为90%。相比之下,他们对BPA的潜在暴露主要通过饮食摄入:两个州的儿童均为99%。根据儿童尿液中排出量计算出的他们对PCP的估计暴露量,比根据多介质PCP浓度计算出的估计最大潜在摄入量高出10倍以上。PCP的这种不一致性凸显了需要进一步研究PCP暴露的环境途径和路线、调查可能接触到的其他可代谢为PCP的化合物,以及研究这种酚类在超过48小时时间段内的人体吸收、代谢和排泄情况。