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Dermal uptake of chemicals

机译:皮肤吸收化学物质

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Biomonitoring has revealed the signatures of hundreds of chemicals in human blood and excreta. Prevention of exposures, which is central to environmental health policy and practice, requires that relevant routes and pathways be understood. Some existing studies that encompass both environmental and biological monitoring provide the opportunity to test aggregate exposure models. A frequent outcome is a shortfall between predicted dose based on environmental measurements and apparent dose estimated from biomarker data. One possible explanation for under-prediction of dermal dose is direct use of results of batch absorption experiments expressed as fractional availability. Because fractional availabilities obtained in this manner are routinely less than those observed via inhalation or ingestion, dermal exposure has often been discounted. However, low apparent availabilities may be an artifact of poorly designed or interpreted experiments. Even low rates of chemical uptake via the skin can account for a non-negligible fraction of a biomonitoring-based dose estimate if exposure is chronic and involves substantial skin area. Regulatory initiatives such as REACH have fostered demand for methods for systematic evaluation of human exposures to commercial chemicals, including many found in consumer products applied directly to the skin. Given prior experience, reconsideration of traditional approaches to assessment of dermal exposure is necessary. Dermal absorption is described as gradient driven transport through a membrane. Observed shortfalls in specific aggregate exposure case studies provide a basis for evaluating physical constants needed to characterize dermal dose. Overall mass transfer coefficients reflecting total resistance to transport from the environment to clothing, from clothing to skin, and from the skin surface to systemic circulation can be generated from these studies and compared to estimates derived from understanding of component processes. Once adequate cases have been developed, chemical screening capability will be improved.
机译:生物监测揭示了人类血液和排泄物中数百种化学物质的特征。预防接触是环境卫生政策和实践的核心,需要了解相关的途径和途径。现有的一些涵盖环境和生物监测的研究提供了测试总体暴露模型的机会。常见的结果是基于环境测量的预测剂量与根据生物标志物数据估算的表观剂量之间的差值。皮肤剂量预测不足的一种可能解释是直接使用表示为可用分数的批次吸收实验结果。由于以这种方式获得的部分利用率通常比通过吸入或摄入所观察到的利用率低,因此皮肤暴露通常被打折。但是,表观可用性低可能是设计或解释不当的实验的产物。如果暴露是长期的并且涉及大量皮肤区域,那么即使是通过皮肤的化学吸收率低,也可以解释基于生物监测的剂量估计中不可忽略的部分。诸如REACH之类的监管举措已经促使人们对系统评估人体暴露于商业化学品的方法的需求,其中包括直接应用于皮肤的消费品中发现的许多方法。根据先前的经验,有必要重新考虑评估皮肤接触的传统方法。皮肤吸收被描述为通过膜的梯度驱动的转运。在具体的总体暴露案例研究中观察到的不足为评估表征皮肤剂量所需的物理常数提供了基础。可以从这些研究中得出反映从环境到衣服,从衣服到皮肤,从皮肤表面到系统循环的总阻力的总体传质系数,并将其与从对组成过程的理解中得出的估计值进行比较。一旦确定了足够的病例,化学筛查能力将得到提高。

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