Evidence map›Paper›PMID 40790337›Full record

ArticleJournal of proteome research2025

Evaluating Novel Direct Injection Liquid Chromatography-Mass Spectrometry Method and Extraction-Based Workflows for Untargeted Lipidomics of Extracellular Vesicles.

Michał Młynarczyk, Felicja Gajdowska, Jorge Matinha-Cardoso, Paulo Oliveira, Paula Tamagnini, Mariusz Belka, Jagoda Mantej, Danuta Gutowska-Owsiak, Weronika Hewelt-Belka

Abstract read
In one paragraph

Article in Journal of proteome research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Michał MłynarczykDepartment of Analytical Chemistry, Faculty of Chemistry, Gdańsk University of Technology, Gdańsk 80-233, Poland.ORCID 0000-0003-3609-4910
Felicja GajdowskaLaboratory of Experimental and Translational Allergology and Pneumology, Medical University of Gdańsk, Gdańsk 80-214, Poland.
Jorge Matinha-CardosoMCbiology Doctoral Program, ICBAS-School of Medicine and Biomedical Sciences Abel Salazar, University of Porto, Porto 4050-313, Portugal.ORCID 0000-0003-4012-0069
Paulo OliveiraCIIMAR-Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Matosinhos 4450-208, Portugal.ORCID 0000-0002-0938-152X
Paula TamagniniI3S-Instituto de Investigação e Inovação em Saúde, University of Porto, Porto 4200-135, Portugal.ORCID 0000-0003-4396-2122
Mariusz BelkaDepartment of Pharmaceutical Chemistry, Medical University of Gdańsk, Gdańsk 80-416, Poland.ORCID 0000-0003-4413-1080
Jagoda MantejLaboratory of Experimental and Translational Allergology and Pneumology, Medical University of Gdańsk, Gdańsk 80-214, Poland.
Danuta Gutowska-OwsiakLaboratory of Experimental and Translational Immunology, Intercollegiate Faculty of Biotechnology of University of Gdańsk and Medical University of Gdańsk, University of Gdańsk, Gdańsk 80-307, Poland.
Weronika Hewelt-BelkaDepartment of Analytical Chemistry, Faculty of Chemistry, Gdańsk University of Technology, Gdańsk 80-233, Poland.ORCID 0000-0002-1990-2130

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipids of extracellular vesicles (EVs) are attracting attention due to their crucial biological functions and potential roles in processes such as carcinogenesis. This study compares three commonly used lipid extraction techniques, i.e., liquid-liquid extraction, single-phase extraction, and solid-phase extraction, with a novel direct injection liquid chromatography-mass spectrometry (DI-LC-MS) workflow tailored to EV lipidomics. In the DI-LC-MS approach, EVs are disrupted and released directly in the chromatographic system, enabling the analysis of lipids without a prior extraction step. The applicability of the DI-LC-MS workflow was demonstrated by profiling lipids in mammalian and bacterial EVs. The lipidome coverage and high precision of the DI-LC-MS method (coefficient of variation of peak area lower than 20% for all the identified lipids) enabled identification of differences in lipid profiles of EV samples. The column used in the DI-LC-MS method exhibited a sufficient lifespan and stability for comparative lipidomic studies. Lipidome coverage, lipid species distribution, and precision varied across the studied workflows; our findings highlight the strengths and limitations of these methods. The DI-LC-MS emerges as a sustainable alternative for EV lipidomic studies by eliminating the need for sample preparation and reducing analysis time, solvent use, and chemical noise while requiring less than 1 μL of sample.

Indexed as

Extracellular VesiclesLipidomicsLipidsMass SpectrometryAnimalsChromatography, LiquidHumansLiquid Chromatography-Mass SpectrometryLiquid-Liquid ExtractionSolid Phase ExtractionWorkflowLipidsextracellular vesiclesLC-MSlipid extractionlipidomicsliquid–liquid extractionsolid-phase extraction

Identifiers

PMID40790337
PMCPMC12604029

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.