LC-MS-Based Global Metabolic Profiles of Alternative Blood Specimens Collected by Microsampling

Blood microsampling (BμS) has recently emerged as an interesting approach in the analysis of endogenous metabolites but also in metabolomics applications. Their non-invasive way of use and the simplified logistics that they offer renders these technologies highly attractive in large-scale studies, especially the novel quantitative microsampling approaches such as VAMs or qDBS. <b>Objectives:</b> Herein, we investigate the potential of BµS devices compared to the conventional plasma samples used in global untargeted mass spectrometry-based metabolomics of blood. <b>Methods:</b> Two novel quantitative devices, namely, Mitra, Capitainer, and the widely used Whatman cards, were selected for comparison with plasma. Venous blood was collected from 10 healthy, overnight-fasted individuals and loaded on the devices; plasma was also collected from the same venous blood. An extraction solvent optimization study was first performed on the three devices before the main study, which compared the global metabolic profiles of the four extracts (three BµS devices and plasma). Analysis was conducted using reverse phase LC-TOF MS in positive mode. <b>Results:</b> BµS devices, especially Mitra and Capitainer, provided equal or even superior information on the metabolic profiling of human blood based on the number and intensity of features and the precision and stability of some annotated metabolites compared to plasma. Despite their rich metabolic profiles, BµS did not capture metabolites associated with biological differentiation of sexes. <b>Conclusions:</b> Overall, our results suggest that a more in-depth investigation of the acquired information is needed for each specific application, as a metabolite-dependent trend was obvious.

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Publication Details

Journal
Metabolites
Published
2025-01-16
DOI
https://doi.org/10.3390/metabo15010062
Citations
10
Primary Topic
Metabolomics and Mass Spectrometry Studies
Type
article
Field-Weighted Citation Impact
8.06

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article

LC-MS-Based Global Metabolic Profiles of Alternative Blood Specimens Collected by Microsampling

Georgios Theodoridis, Vassilis Mougios, Anatoli Petridou, Helen Gika et al.
10 citations
Metabolites
Metabolomics and Mass Spectrometry Studies
8.06
article

LC-MS-Based Global Metabolic Profiles of Alternative Blood Specimens Collected by Microsampling

Georgios Theodoridis, Vassilis Mougios, Anatoli Petridou, Helen Gika, Marlene Thaitumu, Daniel Marques de Sá e Silva, Johannes Rainer, Philippine Louail, Glykeria Avgerinou
article en
10 citations

Abstract

Blood microsampling (BμS) has recently emerged as an interesting approach in the analysis of endogenous metabolites but also in metabolomics applications. Their non-invasive way of use and the simplified logistics that they offer renders these technologies highly attractive in large-scale studies, especially the novel quantitative microsampling approaches such as VAMs or qDBS. <b>Objectives:</b> Herein, we investigate the potential of BµS devices compared to the conventional plasma samples used in global untargeted mass spectrometry-based metabolomics of blood. <b>Methods:</b> Two novel quantitative devices, namely, Mitra, Capitainer, and the widely used Whatman cards, were selected for comparison with plasma. Venous blood was collected from 10 healthy, overnight-fasted individuals and loaded on the devices; plasma was also collected from the same venous blood. An extraction solvent optimization study was first performed on the three devices before the main study, which compared the global metabolic profiles of the four extracts (three BµS devices and plasma). Analysis was conducted using reverse phase LC-TOF MS in positive mode. <b>Results:</b> BµS devices, especially Mitra and Capitainer, provided equal or even superior information on the metabolic profiling of human blood based on the number and intensity of features and the precision and stability of some annotated metabolites compared to plasma. Despite their rich metabolic profiles, BµS did not capture metabolites associated with biological differentiation of sexes. <b>Conclusions:</b> Overall, our results suggest that a more in-depth investigation of the acquired information is needed for each specific application, as a metabolite-dependent trend was obvious.

MetabolitesVol. 15(1)
Eurac Research (IT), Aristotle University of Thessaloniki (GR), Institute for Biomedicine (IT)
European Commission, Aristotle University of Thessaloniki
Openalex Percentile: Top 2%
Metabolomics and Mass Spectrometry Studies
8.06
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