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作为 HBM4EU 质量保证计划的一部分,用于血清中全氟烷基物质 (PFAS) 人体生物监测的实验室间比较研究 (ICIs) 和外部质量保证计划 (EQUASs)。

Interlaboratory Comparison Investigations (ICIs) and External Quality Assurance Schemes (EQUASs) for human biomonitoring of perfluoroalkyl substances (PFASs) in serum as part of the quality assurance programme under HBM4EU.

机构信息

Friedrich-Alexander Universität Erlangen-Nürnberg, Institute and Outpatient Clinic of Occupational, Social and Environmental Medicine, Henkestraße 9-11, 91054 Erlangen, Germany.

National Center for Environmental Health, Instituto de Salud Carlos III, Ctra. Majadahonda a Pozuelo km2,2, 28220 Madrid, Spain.

出版信息

Sci Total Environ. 2022 Nov 15;847:157481. doi: 10.1016/j.scitotenv.2022.157481. Epub 2022 Jul 20.

DOI:10.1016/j.scitotenv.2022.157481
PMID:35868372
Abstract

Perfluoroalkyl substances (PFASs) are of very high concern due to their persistence and accumulative behaviour as well as their manifold adverse health effects. Human biomonitoring (HBM) based on the determination of PFASs in serum samples is an adequate and established strategy for exposure and risk assessment of the population. The suspected health risks associated with exposure levels in the general population call for reliable HBM data verified by Quality Assurance and Quality Control (QA/QC) measures. PFASs were among the chemicals selected as priority substances in HBM4EU, a pan-European project to harmonize and advance HBM within 30 European countries. For this purpose, the analytical comparability and accuracy of PFASs-analysing laboratories was assessed in a QA/QC programme comprising Interlaboratory Comparison Investigations (ICIs) and External Quality Assurance Schemes (EQUASs). This paper presents the evaluation process and discusses the results of four ICI/EQUAS rounds for the determination of eight perfluoroalkyl carboxylic acids and four perfluoroalkyl sulfonic acids (PFBS, PFHxS, PFHpS, PFOS) in serum. All 21 participating laboratories achieved satisfactory results for at least six of these biomarkers, although low limits of quantification (of about 0.1 μg/L) were required to quantify serum PFAS levels at general population exposure levels. The mean relative standard deviation of the participants' results (study RSD) significantly improved from 22 % to 13 % over all PFAS biomarkers in the course of the four rounds. This QA/QC programme succeeded in establishing a network of laboratories with high analytical comparability and accuracy for the analysis of PFASs across 12 European countries.

摘要

全氟烷基物质(PFAS)因其持久性和累积性以及多种不良健康影响而备受关注。基于血清样本中 PFAS 测定的人体生物监测(HBM)是评估人群暴露和风险的一种充分且已建立的策略。由于一般人群接触水平与健康风险之间存在关联,因此需要通过质量保证和质量控制(QA/QC)措施来验证可靠的 HBM 数据。PFAS 是 HBM4EU 作为优先物质选定的化学物质之一,HBM4EU 是一个泛欧项目,旨在协调和推进 30 个欧洲国家的 HBM。为此,在一项包含实验室间对比研究(ICIs)和外部质量保证计划(EQUAS)的 QA/QC 方案中,评估了分析 PFAS 实验室的分析可比性和准确性。本文介绍了评估过程,并讨论了四次 ICI/EQUAS 轮次用于血清中八种全氟烷基羧酸和四种全氟烷基磺酸(PFBS、PFHxS、PFHpS、PFOS)测定的结果。尽管需要低至约 0.1 μg/L 的定量下限才能在一般人群暴露水平下量化血清 PFAS 水平,但所有 21 家参与实验室均至少对其中六种生物标志物取得了令人满意的结果。在四轮研究中,参与者结果的平均相对标准偏差(研究 RSD)显著从 22%提高到所有 PFAS 生物标志物的 13%。该 QA/QC 方案成功建立了一个网络,其中包含 12 个欧洲国家的分析实验室,它们在分析 PFAS 方面具有高度的分析可比性和准确性。

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