Evaluation of a liquid electron ionization liquid chromatography-mass spectrometry interface

J Chromatogr A. 2019 Apr 26:1591:120-130. doi: 10.1016/j.chroma.2019.01.034. Epub 2019 Jan 11.

Abstract

Liquid Electron Ionization (LEI), is an innovative liquid chromatography-mass spectrometry (LC-MS) interface that converts liquid HPLC eluent to the gas-phase in a mass spectrometer equipped with an electron ionization (EI) source. LEI extends the electronic spectra libraries access to liquid chromatography, providing a powerful tool in the untargeted approacssh. Negligible matrix effects allow accurate quantitative information. The purpose of this research was to evaluate the main aspects concerning the interfacing process. These fundamental studies were necessary to understand the mechanism of LEI in details, and improve the interfacing process, especially regarding robustness and sensitivity. Hardware components were installed to prevent analytes precipitation, reduce thermal decomposition of sensitive compounds, and to stabilize the nano-flow delivery with different mobile-phase compositions. Particular attention was devoted to insulating the heated vaporization area from the LC part of the system. Experiments were performed to optimize the interface inner capillary dimensions, and other operative parameters, including temperature, gas and liquid flow rates. Test compounds of environmental interest were selected based on molecular weight, thermal stability, volatility, and polarity. Robustness was evaluated with a set of replicated injections and calibration experiments using a soil matrix as a test sample. MRM detection limits in the low-picogram range were obtained for five pesticides belonging to different classes in a soil sample. High-quality electron ionization mass spectra of a mixture of pesticides were also obtained.

Keywords: Electron ionization; LC–MS interface; Liquid chromatography; Liquid electron ionization (LEI); Mass spectrometry; Matrix effects.

MeSH terms

  • Chromatography, High Pressure Liquid / methods*
  • Deoxycholic Acid / analysis
  • Electrons*
  • Imatinib Mesylate / analysis
  • Limit of Detection
  • Mass Spectrometry / methods*
  • Reproducibility of Results
  • Signal-To-Noise Ratio
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Deoxycholic Acid
  • Imatinib Mesylate