Nassazzi Winnie, Lai Foon Yin, Ahrens Lutz
Department of Aquatic Sciences and Assessment, Swedish University Agricultural Sciences (SLU), Box 7050, SE-750 07 Uppsala, Sweden.
Department of Aquatic Sciences and Assessment, Swedish University Agricultural Sciences (SLU), Box 7050, SE-750 07 Uppsala, Sweden.
J Chromatogr B Analyt Technol Biomed Life Sci. 2022 Dec 1;1212:123514. doi: 10.1016/j.jchromb.2022.123514. Epub 2022 Oct 22.
Per- and polyfluoroalkyl substances (PFAS) are chemicals of concern due to their persistence, bioaccumulation, and toxic properties. PFAS accumulation in plants poses a risk of human and animal exposure due to consumption of the affected plants, but also allows plants to be used in remediation of PFAS-contaminated soils and groundwater. Therefore, effective extraction, cleanup, and analytical methods for measuring PFAS concentrations in plants are fundamental for research on animal and environmental health. PFAS analysis in plant matrices is complex, due to high matrix interference, and scarcity of methods for analyzing different classes of PFAS. In this study, a simple sample preparation method for PFAS analysis in various plant tissues (leaves, needles, twigs, stems, roots from 10 different species) was developed and validated. Instrumental analysis was performed using liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). The method was optimized considering six different extraction conditions and three different cleanup techniques. Methanol as extraction solvent, combined with 1 g ENVI carb cartridges, showed best performance among all extraction conditions and cleanup techniques tested. Method validation showed good recovery (90-120%), high within-day and between-day precision (<20% relative standard deviation), and low method detection limit (0.04-4.8 ng g dry weight (dw)) for different plant matrices. In tests of the method on soil and different plant tissues of silver birch (Betula pendula) and Norway spruce (Picea abies) at a PFAS-contaminated site, 16 of 24 target PFAS were detected in plants and 17 in soil. ƩPFAS concentration in soil was 43 ng g dw. PFAS distribution in silver birch tissues ranged from 7.1 ng g dw in roots to 64 ng g dw in leaves, and in Norway spruce from 14 ng g dw in roots to 16 ng g dw in needles. This novel method for PFAS analysis in plants can be valuable in future monitoring, process understanding, remediation, and risk assessments.
全氟和多氟烷基物质(PFAS)因其持久性、生物累积性和毒性而备受关注。PFAS在植物中的积累不仅会因食用受影响的植物而对人类和动物构成暴露风险,还使得植物可用于修复受PFAS污染的土壤和地下水。因此,用于测量植物中PFAS浓度的有效提取、净化和分析方法是动物和环境健康研究的基础。由于基质干扰大以及分析不同类别PFAS的方法稀缺,植物基质中的PFAS分析较为复杂。在本研究中,开发并验证了一种用于分析各种植物组织(来自10个不同物种的叶子、针叶、嫩枝、茎、根)中PFAS的简单样品制备方法。使用液相色谱-串联质谱联用仪(LC-MS/MS)进行仪器分析。该方法针对六种不同的提取条件和三种不同的净化技术进行了优化。在所有测试的提取条件和净化技术中,甲醇作为提取溶剂并结合1 g ENVI碳柱表现出最佳性能。方法验证表明,对于不同的植物基质,回收率良好(90 - 120%),日内和日间精密度高(相对标准偏差<20%),方法检测限低(0.04 - 4.8 ng g干重(dw))。在一个受PFAS污染场地对土壤以及白桦(Betula pendula)和挪威云杉(Picea abies)的不同植物组织进行该方法测试时,在植物中检测到24种目标PFAS中的16种,在土壤中检测到17种。土壤中总PFAS浓度为43 ng g dw。PFAS在白桦组织中的分布范围从根部的7.1 ng g dw到叶子的64 ng g dw,在挪威云杉中从根部的14 ng g dw到针叶的16 ng g dw。这种用于植物中PFAS分析的新方法在未来的监测、过程理解、修复和风险评估中可能具有重要价值。