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dc.date.accessioned2021-10-14T15:32:13Z
dc.date.available2021-10-14T15:32:13Z
dc.date.created2021-08-23T12:56:07Z
dc.date.issued2021
dc.identifier.citationSkogvold, Hanne Bendiksen Sandås, Elise Mørk Østeby, Anja Løkken, Camilla Rootwelt, Helge Rønning, Per Ola Wilson, Steven Ray Haakon Elgstøen, Katja Benedikte Prestø . Bridging the Polar and Hydrophobic Metabolome in Single-Run Untargeted Liquid Chromatography-Mass Spectrometry Dried Blood Spot Metabolomics for Clinical Purposes. Journal of Proteome Research. 2021, 20(8), 4010-4021
dc.identifier.urihttp://hdl.handle.net/10852/88931
dc.description.abstractDried blood spot (DBS) metabolite analysis is a central tool for the clinic, e.g., newborn screening. Instead of applying multiple analytical methods, a single liquid chromatography-mass spectrometry (LC–MS) method was developed for metabolites spanning from highly polar glucose to hydrophobic long-chain acylcarnitines. For liquid chromatography, a diphenyl column and a multi-linear solvent gradient operated at elevated flow rates allowed for an even-spread resolution of diverse metabolites. Injecting moderate volumes of DBS organic extracts directly, in contrast to evaporation and reconstitution, provided substantial increases in analyte recovery. Q Exactive MS settings were also tailored for sensitivity increases, and the method allowed for analyte retention time and peak area repeatabilities of 0.1–0.4 and 2–10%, respectively, for a wide polarity range of metabolites (log P −4.4 to 8.8). The method’s performance was suited for both untargeted analysis and targeted approaches evaluated in clinically relevant experiments.
dc.languageEN
dc.publisherACS Publications
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleBridging the Polar and Hydrophobic Metabolome in Single-Run Untargeted Liquid Chromatography-Mass Spectrometry Dried Blood Spot Metabolomics for Clinical Purposes
dc.typeJournal article
dc.creator.authorSkogvold, Hanne Bendiksen
dc.creator.authorSandås, Elise Mørk
dc.creator.authorØsteby, Anja
dc.creator.authorLøkken, Camilla
dc.creator.authorRootwelt, Helge
dc.creator.authorRønning, Per Ola
dc.creator.authorWilson, Steven Ray Haakon
dc.creator.authorElgstøen, Katja Benedikte Prestø
cristin.unitcode185,15,12,63
cristin.unitnameSeksjon for kjemisk livsvitenskap - biomolekyler, bio-inspirerte materialer og bioanalytisk kjemi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1928022
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal of Proteome Research&rft.volume=20&rft.spage=4010&rft.date=2021
dc.identifier.jtitleJournal of Proteome Research
dc.identifier.volume20
dc.identifier.issue8
dc.identifier.startpage4010
dc.identifier.endpage4021
dc.identifier.doihttps://doi.org/10.1021/acs.jproteome.1c00326
dc.identifier.urnURN:NBN:no-91545
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1535-3893
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/88931/2/acs.jproteome.1c00326.pdf
dc.type.versionPublishedVersion


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