Rodrigues Matos Rebecca, Jennings Elaine K, Kaesler Jan, Reemtsma Thorsten, Koch Boris P, Lechtenfeld Oliver J
Department of Environmental Analytical Chemistry, Helmholtz Centre for Environmental Research - UFZ, Permoserstr. 15, 04318 Leipzig, Germany.
Institute of Analytical Chemistry, University of Leipzig, 04103 Leipzig, Germany.
Analyst. 2024 Jun 10;149(12):3468-3478. doi: 10.1039/d4an00119b.
Ultrahigh resolution mass spectrometry hyphenated with liquid chromatography (LC) is an emerging tool to explore the isomeric composition of dissolved organic matter (DOM). However, matrix effects limit the potential for semi-quantitative comparison of DOM molecule abundances across samples. We introduce a post-column infused internal standard (PCI-IS) for reversed-phase LC-FT-ICR MS measurements of DOM and systematically evaluate matrix effects, detector linearity and the precision of mass peak intensities. Matrix effects for model compounds spiked into freshwater DOM samples ranging from a headwater stream to a major river were reduced by 5-10% for PCI-IS corrected mass peak intensities as compared to raw (, untransformed) intensities. A linear regression of PCI-IS corrected DOM mass peak intensities across a typical DOM concentration range (2-15 mg dissolved organic carbon L) in original, non-extracted freshwater samples demonstrates excellent linearity of the detector response ( > 0.9 for 98% of detected molecular formulas across retention times). Importantly, PCI-IS could compensate for 80% of matrix effects across an environmental gradient of DOM composition from groundwater to surface water. This enabled studying the ionization efficiency of DOM isomers and linking the observed differences to the biogeochemical sources. With PCI-IS original, non-extracted DOM samples can be analysed by LC-FT-ICR MS without carbon load adjustment, and mass peak intensities can be reliably used to semi-quantitatively compare isomer abundances between compositionally similar DOM samples.
液相色谱联用超高分辨率质谱(LC)是一种用于探索溶解有机物(DOM)异构体组成的新兴工具。然而,基质效应限制了跨样品进行DOM分子丰度半定量比较的潜力。我们引入了一种用于反相LC-FT-ICR MS测量DOM的柱后注入内标(PCI-IS),并系统地评估了基质效应、检测器线性以及质量峰强度的精度。与原始(未转换)强度相比,对于添加到从源头溪流到主要河流的淡水DOM样品中的模型化合物,PCI-IS校正后的质量峰强度的基质效应降低了5-10%。在原始的、未萃取的淡水样品中,典型DOM浓度范围(2-15 mg溶解有机碳/L)内PCI-IS校正后的DOM质量峰强度的线性回归表明检测器响应具有出色的线性(在保留时间范围内,98%的检测分子式的R²>0.9)。重要的是,PCI-IS可以补偿从地下水到地表水的DOM组成环境梯度中80%的基质效应。这使得能够研究DOM异构体的电离效率,并将观察到的差异与生物地球化学来源联系起来。使用PCI-IS时,无需进行碳负载调整即可通过LC-FT-ICR MS分析原始的、未萃取的DOM样品,并且质量峰强度可可靠地用于半定量比较组成相似的DOM样品之间的异构体丰度。