Department of Applied Environmental Science (ITM), Stockholm University, 10691 Stockholm, Sweden.
Anal Bioanal Chem. 2011 Jun;400(6):1625-35. doi: 10.1007/s00216-011-4823-8. Epub 2011 Mar 12.
Recent developments, improvements, and trends in the ultra-trace determination of per- and polyfluoroalkyl substances (PFASs) in environmental and human samples are highlighted and the remaining challenges and uncertainties are outlined and discussed. Understanding the analytical implications of such things as adsorption of PFASs to surfaces, effects of differing matrices, varying PFAS isomer response factors, potential bias effects of sampling, sample preparation, and analysis is critical to measuring highly fluorinated compounds at trace levels. These intricate analytical issues and the potential consequences of ignoring to deal with them correctly are discussed and documented with examples. Isomer-specific analysis and the development of robust multi-chemical methods are identified as topical trends in method development for an ever-increasing number of PFASs of environmental and human interest. Ultimately, the state-of-the-art of current analytical method accuracy is discussed on the basis of results from interlaboratory comparison studies.
本文重点介绍了环境和人体样本中痕量至超痕量全氟和多氟烷基物质(PFASs)的最新发展、改进和趋势,并概述和讨论了尚存的挑战和不确定性。了解 PFASs 表面吸附、不同基质的影响、不同 PFAS 异构体响应因子的变化、采样、样品制备和分析过程中的潜在偏倚效应等因素对痕量水平下高度氟化化合物的测量具有重要意义。本文讨论并举例说明了这些复杂的分析问题以及未能正确处理这些问题可能带来的潜在后果。对于环境和人体关注的 PFASs 数量不断增加,异构体特异性分析和稳健的多化学方法的开发被确定为方法开发的热门趋势。最终,根据实验室间比较研究的结果,讨论了当前分析方法准确性的最新进展。