Evidence map›Paper›PMID 31074960›Full record

ArticleAnalytical chemistry2019

A Comprehensive UHPLC Ion Mobility Quadrupole Time-of-Flight Method for Profiling and Quantification of Eicosanoids, Other Oxylipins, and Fatty Acids.

Christine Hinz, Sonia Liggi, Gabriele Mocciaro, Stephanie Jung, Isuru Induruwa, Milton Pereira, Clare E Bryant, Sven W Meckelmann, Valerie B O'Donnell, Richard W Farndale and 2 more

Abstract read
In one paragraph

Article in Analytical chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Oxidised Apolipoprotein Peptidome Characterises Metabolic Dysfunction-Associated Steatotic Liver Disease.Liver international : official journal of the International Association for the Study of the Liver · 2025
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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

12 authors.

Christine HinzDepartment of Biochemistry and Cambridge Systems Biology Centre , University of Cambridge , Cambridge CB2 1GA , United Kingdom.
Sonia LiggiDepartment of Biochemistry and Cambridge Systems Biology Centre , University of Cambridge , Cambridge CB2 1GA , United Kingdom.ORCID 0000-0003-1802-357X
Gabriele MocciaroDepartment of Biochemistry and Cambridge Systems Biology Centre , University of Cambridge , Cambridge CB2 1GA , United Kingdom.
Stephanie JungDepartment of Biochemistry , University of Cambridge , Downing Site, Cambridge CB2 1QW , United Kingdom.
Isuru InduruwaDepartment of Clinical Neurosciences , University of Cambridge , Cambridge CB2 0QQ , United Kingdom.
Milton PereiraDepartment of Veterinary Medicine , University of Cambridge , Cambridge CB3 0ES , United Kingdom.
Clare E BryantDepartment of Veterinary Medicine , University of Cambridge , Cambridge CB3 0ES , United Kingdom.
Sven W MeckelmannFaculty of Chemistry, Applied Analytical Chemistry , University of Duisburg-Essen , 45141 Essen , Germany.
Valerie B O'DonnellSystems Immunity Research Institute , Cardiff University , Cardiff CF14 4XN , United Kingdom.
Richard W FarndaleDepartment of Biochemistry , University of Cambridge , Downing Site, Cambridge CB2 1QW , United Kingdom.
John FjeldstedAgilent Technologies , Santa Clara , California 95051 , United States.
Julian L GriffinDepartment of Biochemistry and Cambridge Systems Biology Centre , University of Cambridge , Cambridge CB2 1GA , United Kingdom.ORCID 0000-0003-1336-7744

Funding

Optimized Metabolite Extraction, Separation, and Identification for MetabolomicsR01ES022186 · NIEHS · PENNSYLVANIA STATE UNIVERSITY, THE · PI PATTERSON, ANDREW · 2012 to 2016
$2.0M
British Heart Foundation PG/10/011/28199British Heart Foundation RG/15/4/31268British Heart Foundation SP/13/7/30575Medical Research Council MR/P011705/1Medical Research Council MR/P01836X/1NIEHS NIH HHS R01 ES022186Wellcome Trust 108045Wellcome Trust 108045/Z/15/Z
6 · The paper itself

Abstract

Analysis of oxylipins by liquid chromatography mass spectrometry (LC/MS) is challenging because of the small mass range occupied by this diverse lipid class, the presence of numerous structural isomers, and their low abundance in biological samples. Although highly sensitive LC/MS/MS methods are commonly used, further separation is achievable by using drift tube ion mobility coupled with high-resolution mass spectrometry (DTIM-MS). Herein, we present a combined analytical and computational method for the identification of oxylipins and fatty acids. We use a reversed-phase LC/DTIM-MS workflow able to profile and quantify (based on chromatographic peak area) the oxylipin and fatty acid content of biological samples while simultaneously acquiring full scan and product ion spectra. The information regarding accurate mass, collision-cross-section values in nitrogen (

Indexed as

AnimalsCells, CulturedChromatography, High Pressure LiquidEicosanoidsFatty AcidsHumansIon Mobility SpectrometryMice, Inbred C57BLOxylipinsTandem Mass SpectrometryEicosanoidsFatty AcidsOxylipins

Identifiers

PMID31074960
PMCPMC7613057

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Registered trials

None linked

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.