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dc.date.accessioned2022-03-19T18:18:19Z
dc.date.available2022-03-19T18:18:19Z
dc.date.created2021-08-26T15:20:56Z
dc.date.issued2021
dc.identifier.citationAmbaw, Yohannes Abere Dahl, Sandra Rinne Chen, Yan Greibrokk, Tyge Lundanes, Elsa Lazraq, Issam Shinde, Sudhirkumar Selvalatchmanan, Jayashree Wenk, Markus R. Sellergren, Börje Torta, Federico . Tailored polymer-based selective extraction of lipid mediators from biological samples. Metabolites. 2021, 11(8), 1-14
dc.identifier.urihttp://hdl.handle.net/10852/92655
dc.description.abstractLipid mediators, small molecules involved in regulating inflammation and its resolution, are a class of lipids of wide interest as their levels in blood and tissues may be used to monitor health and disease states or the effect of new treatments. These molecules are present at low levels in biological samples, and an enrichment step is often needed for their detection. We describe a rapid and selective method that uses new low-cost molecularly imprinted (MIP) and non-imprinted (NIP) polymeric sorbents for the extraction of lipid mediators from plasma and tissue samples. The extraction process was carried out in solid-phase extraction (SPE) cartridges, manually packed with the sorbents. After extraction, lipid mediators were quantified by liquid chromatography–tandem mass spectrometry (LC–MSMS). Various parameters affecting the extraction efficiency were evaluated to achieve optimal recovery and to reduce non-specific interactions. Preliminary tests showed that MIPs, designed using the prostaglandin biosynthetic precursor arachidonic acid, could effectively enrich prostaglandins and structurally related molecules. However, for other lipid mediators, MIP and NIP displayed comparable recoveries. Under optimized conditions, the recoveries of synthetic standards ranged from 62% to 100%. This new extraction method was applied to the determination of the lipid mediators concentration in human plasma and mouse tissues and compared to other methods based on commercially available cartridges. In general, the methods showed comparable performances. In terms of structural specificity, our newly synthesized materials accomplished better retention of prostaglandins (PGs), hydroxydocosahexaenoic acid (HDoHE), HEPE, hydroxyeicosatetraenoic acids (HETE), hydroxyeicosatrienoic acid (HETrE), and polyunsaturated fatty acid (PUFA) compounds, while the commercially available Strata-X showed a higher recovery for dihydroxyeicosatetraenoic acid (diHETrEs). In summary, our results suggest that this new material can be successfully implemented for the extraction of lipid mediators from biological samples.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleTailored polymer-based selective extraction of lipid mediators from biological samples
dc.typeJournal article
dc.creator.authorAmbaw, Yohannes Abere
dc.creator.authorDahl, Sandra Rinne
dc.creator.authorChen, Yan
dc.creator.authorGreibrokk, Tyge
dc.creator.authorLundanes, Elsa
dc.creator.authorLazraq, Issam
dc.creator.authorShinde, Sudhirkumar
dc.creator.authorSelvalatchmanan, Jayashree
dc.creator.authorWenk, Markus R.
dc.creator.authorSellergren, Börje
dc.creator.authorTorta, Federico
cristin.unitcode185,15,12,0
cristin.unitnameKjemisk institutt
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1929041
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Metabolites&rft.volume=11&rft.spage=1&rft.date=2021
dc.identifier.jtitleMetabolites
dc.identifier.volume11
dc.identifier.issue8
dc.identifier.doihttps://doi.org/10.3390/metabo11080539
dc.identifier.urnURN:NBN:no-95229
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2218-1989
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/92655/1/metabolites-11-00539-v2.pdf
dc.type.versionPublishedVersion
cristin.articleid539


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