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dc.contributor.authorSkogvold, Hanne Bendiksen
dc.contributor.authorSandås, Elise Mørk
dc.contributor.authorØsteby, Anja
dc.contributor.authorLøkken, Camilla
dc.contributor.authorRootwelt, Helge
dc.contributor.authorRønning, Per Ola
dc.contributor.authorWilson, Steven Ray Haakon
dc.contributor.authorElgstøen, Katja Benedikte Prestø
dc.date.accessioned2021-10-12T07:29:10Z
dc.date.available2021-10-12T07:29:10Z
dc.date.created2021-08-23T12:56:07Z
dc.date.issued2021
dc.identifier.citationJournal of Proteome Research. 2021, 20 (8), 4010-4021.en_US
dc.identifier.issn1535-3893
dc.identifier.urihttps://hdl.handle.net/11250/2789130
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.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectMetabolomicsen_US
dc.subjectDried blood spotsen_US
dc.subjectLiquid chromatography-mass spectrometryen_US
dc.titleBridging the polar and hydrophobicmMetabolome in single-run untargeted liquid chromatography-mass spectrometry dried blood spot metabolomics for clinical purposesen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1021/acs.jproteome.1c00326
dc.identifier.cristin1928022
dc.source.journalJournal of Proteome Researchen_US
dc.source.volume20en_US
dc.source.issue8en_US
dc.source.pagenumber4010-4021en_US


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