High-throughput wide dynamic range procedure for the simultaneous quantification of nicotine and cotinine in multiple biological matrices using hydrophilic interaction liquid chromatography-tandem mass spectrometry

dc.contributor.authorPérez Ortuño, Raúl
dc.contributor.authorMartínez Sánchez, José M.
dc.contributor.authorFernández Muñoz, Esteve
dc.contributor.authorPascual, José Antonio
dc.date.accessioned2020-11-12T11:34:05Z
dc.date.available2020-11-12T11:34:05Z
dc.date.issued2015-09-05
dc.date.updated2020-11-12T11:34:06Z
dc.description.abstractA straightforward, high-throughput method was developed and fully validated for the simultaneous determination of the specific tobacco biomarkers nicotine and its main metabolite cotinine in a wide dynamic range and supporting the most common human biological matrices (urine, oral fluid and hair). Sample preparation was performed inside the very HPLC injection vials by pipetting 0.5 mL of the liquid samples, deuterated internal standards in alkaline solution and dichloromethane as extraction solvent. Solid samples (i.e. around 10 mg hair) were first submitted to alkaline digestion in the HPLC vials and processed accordingly. The organic phase (reached through the upper aqueous layer) was directly injected without further treatment. Instrumental analysis was performed using hydrophilic interaction (HILIC) ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Total chromatographic time was 2 min. The method covers a wide dynamic range making it fit-for-purpose for the analysis of samples covering entire populations, irrespective of the level of exposure or tobacco use. Calibration curves (r 2 > 0.995) covered the range 1-2000 ng/mL (or 0.05-100 ng/mg hair) for nicotine and 0.1-2000 ng/mL (or 0.005-100 ng/mg hair) for cotinine. Within-run and between-run precision and accuracy were typically below 10 %, and always below 20 % at the lower limit of quantification. The method was successfully applied to the analysis of samples from different projects involving multiple matrices.
dc.format.extent11 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec656863
dc.identifier.issn1618-2642
dc.identifier.pmid26342312
dc.identifier.urihttps://hdl.handle.net/2445/171983
dc.language.isoeng
dc.publisherSpringer Verlag
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1007/s00216-015-8993-7
dc.relation.ispartofAnalytical and Bioanalytical Chemistry, 2015, vol. 407, p. 8463-8473
dc.relation.urihttps://doi.org/10.1007/s00216-015-8993-7
dc.rights(c) Springer Verlag, 2015
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Ciències Clíniques)
dc.subject.classificationEspectrometria de masses
dc.subject.classificationNicotina
dc.subject.classificationMarcadors bioquímics
dc.subject.otherMass spectrometry
dc.subject.otherNicotine
dc.subject.otherBiochemical markers
dc.titleHigh-throughput wide dynamic range procedure for the simultaneous quantification of nicotine and cotinine in multiple biological matrices using hydrophilic interaction liquid chromatography-tandem mass spectrometry
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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