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dc.contributor.authorHegstad, Solfrid
dc.contributor.authorHavnen, Hilde
dc.contributor.authorHelland, Arne
dc.contributor.authorFalch, Berit Margrethe Hasle
dc.contributor.authorSpigset, Olav
dc.date.accessioned2018-01-30T09:38:05Z
dc.date.available2018-01-30T09:38:05Z
dc.date.created2017-10-31T15:32:06Z
dc.date.issued2017
dc.identifier.citationJournal of chromatography. B. 2017, 1061-1062 103-109.nb_NO
dc.identifier.issn1570-0232
dc.identifier.urihttp://hdl.handle.net/11250/2480573
dc.description.abstractA method for enantiomeric separation and quantification of R/S-citalopram in serum was developed and validated using ultra-high performance supercritical fluid chromatography-tandem mass spectrometry (UHPSFC-MS/MS). Sample preparation prior to UHPSFC-MS/MS analysis consisted of protein precipitation with acidic acetonitrile and filtration through a phospholipid removal plate. The UHPSFC-MS/MS method used an UPC2 Trefoil CEL2 column with a mobile phase consisting of CO2 and methanol/acetonitrile (70:30, v/v) with 10 mM ammonium acetate. The injection volume was 1 μL and run time was 4 min. MS/MS detection was performed with positive electrospray ionization and two multiple reaction monitoring transitions (m/z 325.1 > 262.0 and m/z 325.1 > 109.0). The calibration range was 5–500 nM for each analyte. The between-assay relative standard deviations were in the range of 3.4–4.5%. Recovery was 81–91% and matrix effects ranged from 96 to 101% (corrected with internal standard). After development and initial testing, the method has been successfully implemented in routine use in our laboratory for both separation and quantification of R/S-citalopram in more than 250 serum samples for therapeutic drug monitoring.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleEnantiomeric separation and quantification of citalopram in serum by ultra-high performance supercritical fluid chromatography-tandem mass spectrometrynb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber103-109nb_NO
dc.source.volume1061-1062nb_NO
dc.source.journalJournal of chromatography. Bnb_NO
dc.identifier.doi10.1016/j.jchromb.2017.07.009
dc.identifier.cristin1509454
dc.description.localcode© 2017. This is the authors’ accepted and refereed manuscript to the article. Locked until 9.7.2019 due to copyright restrictions. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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