Fast, general-purpose metabolome analysis by mixed-mode liquid chromatography–mass spectrometry

Comprehensive metabolomics requires robust and efficient analytical techniques capable of addressing the chemical diversity, complexity, and high sample throughput demands characteristic of large-scale studies. We introduce a rapid, mixed-mode liquid chromatography method that uniquely integrates anion exchange and hydrophobic interactions within a single stationary phase. Employing an optimized ternary gradient, our method achieves comprehensive separation of diverse metabolite classes over a wide range of polarities within only 4 minutes per run. The performance was tested with standards for <i>ca.</i> 1000 metabolites. For two-thirds of 94 isomeric sets, we could achieve a separation of 2 or more seconds, which is sufficient for correct identification. We demonstrate robustness over 500 consecutive injections of bacterial extracts and with the analysis of complex matrices like plasma, cecum extracts, and urine. Throughout, retention time drifts were <1 s. Our mixed-mode LC-MS approach offers a routine throughput of 360 samples per day per instrument and is ideally suited for studies that require rapid and comprehensive metabolic profiling.

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Publication Details

Journal
The Analyst
Published
2025-01-01
DOI
https://doi.org/10.1039/d5an00641d
Citations
2
Primary Topic
Metabolomics and Mass Spectrometry Studies
Type
article
Field-Weighted Citation Impact
1.61
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article

Fast, general-purpose metabolome analysis by mixed-mode liquid chromatography–mass spectrometry

Mário S. P. Correia, Alaa Othman, Nicola Zamboni
2 citations
The Analyst
Metabolomics and Mass Spectrometry Studies
1.61
article

Fast, general-purpose metabolome analysis by mixed-mode liquid chromatography–mass spectrometry

Mário S. P. Correia, Alaa Othman, Nicola Zamboni
article en
2 citations

Abstract

Comprehensive metabolomics requires robust and efficient analytical techniques capable of addressing the chemical diversity, complexity, and high sample throughput demands characteristic of large-scale studies. We introduce a rapid, mixed-mode liquid chromatography method that uniquely integrates anion exchange and hydrophobic interactions within a single stationary phase. Employing an optimized ternary gradient, our method achieves comprehensive separation of diverse metabolite classes over a wide range of polarities within only 4 minutes per run. The performance was tested with standards for <i>ca.</i> 1000 metabolites. For two-thirds of 94 isomeric sets, we could achieve a separation of 2 or more seconds, which is sufficient for correct identification. We demonstrate robustness over 500 consecutive injections of bacterial extracts and with the analysis of complex matrices like plasma, cecum extracts, and urine. Throughout, retention time drifts were <1 s. Our mixed-mode LC-MS approach offers a routine throughput of 360 samples per day per instrument and is ideally suited for studies that require rapid and comprehensive metabolic profiling.

The AnalystVol. 150(22)
ETH Zurich (CH), SwissLitho (Switzerland) (CH)
Openalex Percentile: Top 15%
Metabolomics and Mass Spectrometry Studies
1.61
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