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dc.contributor.authorAndreassen, Trine Naalsund
dc.contributor.authorHavnen, Hilde
dc.contributor.authorSpigset, Olav
dc.contributor.authorFalch, Berit Margrethe Hasle
dc.contributor.authorSkråstad, Ragnhild Bergene
dc.date.accessioned2018-01-23T11:50:00Z
dc.date.available2018-01-23T11:50:00Z
dc.date.created2018-01-03T11:36:56Z
dc.date.issued2017
dc.identifier.issn0146-4760
dc.identifier.urihttp://hdl.handle.net/11250/2479034
dc.description.abstractPhosphatidylethanol (PEth) is an alcohol biomarker formed in the presence of ethanol in the body. Both due to its specificity and because it has a detection window of up to several weeks after alcohol intake, its application potential is broader than for other ethanol biomarkers. The aim of this study was to develop and validate a robust method for PEth in whole blood with fast and efficient sample extraction and a short analytical runtime, suitable for high throughput routine purposes. A validated ultra-performance liquid chromatography tandem mass spectrometry (UPLC®-MSMS) method for quantification of PEth 16:0/18:1 in the range 0.05–4.00 μM (R2 ≥ 0.999) is presented. PEth 16:0/18:1 and the internal standard (IS) PEth-d5 (0.55 μM), were extracted from whole blood (150 μL) by simple protein precipitation with 2-propanol (450 μL). Chromatography was achieved using a BEH-phenyl (2.1 × 30 mm, 1.7 μm) column and a gradient elution combining ammonium formate (5 mM, pH 10.1) and acetonitrile at a flow rate of 0.5 mL/min. Runtime was 2.3 min. The mass spectrometer was monitored in negative mode with multiple reaction monitoring (MRM). The m/z 701.7 > 255.2 and 701.7 > 281.3 transitions were monitored for PEth 16:0/18:1 and the m/z 706.7 > 255.3 for PEth-d5. Limit of quantification was 0.03 μM (coefficient of variation, CV = 6.7%, accuracy = 99.3%). Within-assay and between-assay imprecision were 0.4–3.3% (CV ≤ 7.1%). Recoveries were 95–102% (CV ≤ 4.9%). Matrix effects after IS correction ranged from 107% to 112%. PEth 16:0/18:1 in patient samples were stable for several days at 30°C. Repeated freezing (−80°C) and thawing did not affect the concentration. After thawing and analysis patient samples were stable at 4–8°C for at least 4 weeks. Results from a proficiency test program, showing |Z| values ≤1.2, confirm the validity of the method. Analysis of the first 3,169 samples sent to our laboratory for routine use has demonstrated its properties as a robust method suitable for high throughput purposes.nb_NO
dc.language.isoengnb_NO
dc.publisherOxford University Press (OUP)nb_NO
dc.titleHight throughput UHPC-MSMS method for the analysis of phosphatidylethanol (PEth) 16:0/18:1, a specific biomarker for alcohol consumption, in whole bloodnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.journalJournal of Analytical Toxicologynb_NO
dc.identifier.doi10.1093/jat/bkx075
dc.identifier.cristin1534611
dc.description.localcodePostprint: This is a pre-copyedited, author-produced version of an article accepted for publication in [Journal of Analytical Toxicology following peer review. The version of record [insert complete citation information here] is available online at: [https://academic.oup.com/jat/advance-article/doi/10.1093/jat/bkx075/4103340]. Locked until 4.9.2018 due to copyright restrictions.nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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