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Formic acid pre-treatment enhances untargeted serum and plasma metabolomics

Abstract:

Untargeted metabolic profiling of plasma and serum by liquid chromatography-mass spectrometry (LCMS) is becoming increasingly important in clinical and translational research; however, sample preparation protocols can have a significant impact on study outcomes and there is currently a lack of standardised approaches.

In this study we demonstrate that pre-treatment of serum and plasma samples with 1% formic acid (FA, v/ v) prior to acetonitrile (MeCN)-induced protein precipitation, significantly enhances analytical performance in untargeted metabolomics using reversed-phase liquid chromatography (RPLC)-MS. We show an increase in sample preparation reproducibility and signal intensity across both positive and negative ionisation modes. In two independent serum cohorts (OPTIMA and VITACOG), FA-based extraction improved multivariate modelling (orthogonal partial least squares discriminant analysis, OPLSDA), with consistently higher classification accuracy, sensitivity, and specificity, alongside reduced variability and increased fold-changes in discriminatory compound-features. We investigated factors potentially involved in the enhanced performance and observed outcomes consistent with the disruption of non-covalent protein–metabolite interactions and the stabilisation of labile species. We found no correlation with either protein depletion or differential adduct formation. The results were also not attributable to pH lowering after metabolite extraction.

In this study, we demonstrate that FA pre-treatment of plasma and serum prior to protein precipitation significantly improves sample reproducibility and detection sensitivity in untargeted RPLC-MS metabolomics. This optimised sample preparation strategy offers clear advantages for clinical and translational metabolomics, with strong potential to enhance biomarker discovery and metabolic phenotyping.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1021/acs.analchem.5c03725

Authors


More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Oxford college:
Somerville College
Role:
Author
ORCID:
0000-0002-9477-0182
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author


Publisher:
American Chemical Society
Journal:
Analytical Chemistry More from this journal
Publication date:
2025-10-07
Acceptance date:
2025-09-29
DOI:
EISSN:
1520-6882
ISSN:
0003-2700


Language:
English
Keywords:
Pubs id:
2297057
Local pid:
pubs:2297057
Deposit date:
2025-10-03

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