Evidence map›Paper›PMID 39523922›Full record

ArticleElectrophoresis2025

A Micro-Flow Liquid Chromatography-Mass Spectrometry Method for the Quantification of Oxylipins in Volume-Limited Human Plasma.

Bingshu He, Rawi Ramautar, Marian Beekman, P Eline Slagboom, Amy Harms, Thomas Hankemeier

Abstract read
In one paragraph

Article in Electrophoresis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Bingshu HeMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, The Netherlands.ORCID 0000-0003-1223-4640
Rawi RamautarMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, The Netherlands.ORCID 0000-0002-1673-4848
Marian BeekmanDepartment of Molecular Epidemiology, Leiden University Medical Centre, Leiden, The Netherlands.
P Eline SlagboomDepartment of Molecular Epidemiology, Leiden University Medical Centre, Leiden, The Netherlands.
Amy HarmsDepartment of Molecular Epidemiology, Leiden University Medical Centre, Leiden, The Netherlands.ORCID 0000-0002-2931-4295
Thomas HankemeierMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, The Netherlands.

Funding

China Scholarship Council 201906390032European Union's Seventh Framework Programme 259679Netherlands Consortium for Healthy Ageing 050-060-810Netherlands X-omics Initiative NWO 184.034.019Seventh Framework Programme 259679Vidi grant scheme of the Dutch Research Council (NWO Vidi) 723.016.003ZonMw 457001001
6 · The paper itself

Abstract

Oxylipins are well-known lipid mediators in various inflammatory conditions. Their endogenous concentrations range from low picomolar to nanomolar, and there are growing demands to determine their concentrations in low-volume matrices for pathological studies, including blood, cerebrospinal fluids from animal disease models, infants, and microsampling devices. Most of the published quantification methods for comprehensive profiling of oxylipins still require more than 50 µL plasma as a starting volume to detect these low levels. The aim of our study is to develop a sensitive and reliable method for the quantification of oxylipins in volume-limited human plasma samples. We established and validated a micro-liquid chromatography (LC)-mass spectrometry (MS)/MS method that requires only 5 µL of human plasma for the determination of 66 oxylipins. The optimized micro-LC-MS/MS method utilized a flow rate of 4 µL/min with a 0.3-mm inner diameter column. With an injection volume of 3 µL, our method provides limits of detection in the range from 0.1 to 91.9 pM, and limits of quantification range from 0.3 to 306.2 pM. The sensitivity enhancement compared to conventional flow ranged from 1.4 to 180.7 times for 51 compounds depending on their physical-chemical properties. After validation, the method was applied to analyze 40 plasma samples from a healthy aging study to demonstrate robustness and sensitivity.

Indexed as

OxylipinsTandem Mass SpectrometryChromatography, LiquidHumansLimit of DetectionLinear ModelsLiquid Chromatography-Mass SpectrometryReproducibility of ResultsOxylipinsmicro–liquid chromatography (LC)–mass spectrometry (MS)oxylipinssensitivity enhancementvolume‐limited plasma

Identifiers

PMID39523922
PMCPMC11952279

What Socratic holds

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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 Socratic graph.