4.7 Article

Performance of free-flow field-step electrophoresis as cleanup step for the non-target analysis of environmental water samples

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 414, 期 6, 页码 2189-2204

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03856-w

关键词

Solid-phase extraction; Evaporative concentration; Hydrophilic interaction liquid chromatography; Non-target screening

资金

  1. Projekt DEAL
  2. German Research Foundation (DFG) [SFB 1253/1 2017]

向作者/读者索取更多资源

Efficient sample enrichment and cleanup techniques are crucial for the analysis of low concentrations of micropollutants in environmental water samples. In this study, field-step electrophoresis (FSE) was developed as a cleanup technique for ionizable micropollutants. The FSE/RPLC-MS method exhibited high precision and selectivity for anionic compounds.
For the analysis of low concentrations of micropollutants in environmental water samples, efficient sample enrichment and cleanup are necessary to reduce matrix effects and to reach low detection limits. For analytes of low and medium polarity, solid-phase extraction is used, but robust methods for the preconcentration of highly polar or ionizable analytes are scarce. In this work, field-step electrophoresis (FSE) was developed as an environmental sample cleanup technique for ionizable micropollutants and ionic transformation products. The FSE electrolyte system preconcentrated 15 acidic model analytes (pK(a) from -2.2 to 9.1) present in aqueous samples in two fractions by factors of 5-10. Simultaneously, highly mobile matrix compounds were removed including inorganic ions such as sulfate and chloride. The fractions were either directly injected for downstream analysis by reversed-phase liquid chromatography (RPLC) or further processed by evaporative preconcentration with subsequent reconstitution in an organic solvent suitable for separation methods like hydrophilic interaction chromatography. The FSE/RPLC-MS method exhibited high quantitative precision with RSDs of 3-6%. The method was successfully applied to a spiked river water sample and its performance compared with common solid-phase extraction and evaporative concentration, demonstrating a high analyte coverage. FSE combined with non-target screening by RPLC-MS revealed a strong reduction in matrix load especially at low retention times. Seventeen compounds were identified in the FSE fractions sampled at the field step boundary by retention time, accurate mass, and mass fragments. Suspect screening by FSE/RPLC-MS was facilitated by FSE's selectivity for anionic compounds.

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