Zhang Hongna, Wen Bei, Wen Wen, Ma Yibing, Hu Xiaoyu, Wu Yali, Luo Lei, Zhang Shuzhen
State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Jan 1;1072:25-33. doi: 10.1016/j.jchromb.2017.09.036. Epub 2017 Nov 6.
Isomer-specific analysis of perfluoroalkyl acids (PFAAs) is important to accurately assess their environmental source, fate, and human risks. In this study, a method was developed for the determination of perfluorooctanoic acid (PFOA), perfluorooctane sulfonate (PFOS), and perfluorohexane sulfonate (PFHxS) isomers in biosolids, biosolids-amended soils and plants using ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). The separation efficiencies of two chromatographic columns and extraction capacities of different methods were tested. Compared with the C18 column (ACQUITY UPLC BEH Shield RP18 column), the column with an alkyl perfluorinated C8 stationary phase (Epic FO LB column), in combination with the distinct MS/MS transitions of analytes, allowed better separation of most isomers. The ion-pair extraction method showed more effective matrix separation than that of the alkaline digestion method, with recoveries ranging from 79.6-105% for biosolids, 80.4-116% for soils, and 68.0-114% for plant tissues. The method detection limits ranged from 10 to 55, 3-13, and 8-58pg/g dry weight for biosolids, soil, and plants, respectively. This method was applied successfully to quantify individual isomers in biosolids, biosolids-amended soils and plants. Six PFOA, eight PFOS, and two PFHxS isomers were found in the samples, with linear isomers being the dominant species. Further analysis revealed that the translocation potentials of branched isomers within plants were higher than those of linear isomers.
全氟烷基酸(PFAA)的异构体特异性分析对于准确评估其环境来源、归宿和人类风险至关重要。在本研究中,开发了一种使用超高效液相色谱-串联质谱(UHPLC-MS/MS)测定生物固体、生物固体改良土壤和植物中全氟辛酸(PFOA)、全氟辛烷磺酸(PFOS)和全氟己烷磺酸(PFHxS)异构体的方法。测试了两种色谱柱的分离效率和不同方法的萃取能力。与C18柱(ACQUITY UPLC BEH Shield RP18柱)相比,具有全氟烷基C8固定相的柱(Epic FO LB柱),结合分析物独特的MS/MS跃迁,能更好地分离大多数异构体。离子对萃取法比碱性消化法显示出更有效的基质分离效果,生物固体的回收率为79.6-105%,土壤为80.4-116%,植物组织为68.0-114%。生物固体、土壤和植物的方法检测限分别为10至55、3至13和8至58pg/g干重。该方法成功应用于定量生物固体、生物固体改良土壤和植物中的单个异构体。在样品中发现了六种PFOA、八种PFOS和两种PFHxS异构体,其中线性异构体为主要种类。进一步分析表明,植物内支链异构体的转运潜力高于线性异构体。