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用于改进全氟和多氟烷基物质液相色谱/质谱定量分析的色谱技术

Chromatographic Techniques for Improving the LC/MS Quantification of PFAS.

作者信息

Buckenmaier Stephan, Riemenschneider Christina, Schächtele Alexander, Sölter Susanne

机构信息

Agilent Technologies Deutschland GmbH, Waldbronn, Germany.

State Institute for Chemical and Veterinary Analysis Freiburg, Freiburg, Germany.

出版信息

J Sep Sci. 2025 May;48(5):e70155. doi: 10.1002/jssc.70155.

Abstract

The liquid chromatography / mass spectrometry (LC/MS) quantification of per- and polyfluoroalkyl substances (PFAS) in complex matrices presents challenges. Despite advanced sample preparation techniques to isolate analytes, residual matrix components can still interfere with MS detection. Additionally, extracts often contain high levels of organic solvents limiting the volume that can be injected when using reversed-phase HPLC. Yet, increasing the injection volume could be a simple path to lower detection limits. Feeding PFAS samples, dissolved in pure acetonitrile, at controlled speed into the stream of mobile phase resulted in an analyte focusing effect on the column. By using this approach, the injection volume could be increased 10 times compared to the conventional injection mode, as did the detection sensitivity. Feed injection was coupled to two-dimensional liquid chromatography (2D-LC) in a configuration in which the same triple quadrupole MS could be used for detection in both separation dimensions. The improved separation markedly reduced ion suppression effects and allowed to distinguish the critical PFAS compound perfluorobutanoic acid (PFBA) from isomeric matrix components within tomato extracts interfering with its quantification when only LC/MS was used. This 2D-LC/MS approach therefore fulfilled recommendations that PFBA should be analyzed using a secondary LC approach, without adding a marked amount of time to the analysis.

摘要

在复杂基质中对全氟和多氟烷基物质(PFAS)进行液相色谱/质谱(LC/MS)定量分析存在挑战。尽管采用了先进的样品制备技术来分离分析物,但残留的基质成分仍可能干扰质谱检测。此外,提取物中通常含有高浓度的有机溶剂,这限制了在使用反相高效液相色谱时的进样体积。然而,增加进样体积可能是降低检测限的一条简单途径。将溶解在纯乙腈中的PFAS样品以可控速度注入流动相流中,会在色谱柱上产生分析物聚焦效应。通过使用这种方法,与传统进样模式相比,进样体积可以增加10倍,检测灵敏度也随之提高。进样注入与二维液相色谱(2D-LC)联用,在这种配置中,同一个三重四极杆质谱可用于两个分离维度的检测。改进后的分离显著降低了离子抑制效应,并能够将关键的PFAS化合物全氟丁酸(PFBA)与番茄提取物中的同分异构基质成分区分开来,而仅使用LC/MS时,这些基质成分会干扰PFBA的定量分析。因此,这种二维液相色谱/质谱方法满足了关于应使用二级液相色谱方法分析PFBA的建议,且没有显著增加分析时间。

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