Εμφάνιση απλής εγγραφής

dc.creatorPalaiogiannis D., Bekou E., Pazaitou-Panayiotou K., Samanidou V., Tsakalof A.en
dc.date.accessioned2023-01-31T09:41:21Z
dc.date.available2023-01-31T09:41:21Z
dc.date.issued2017
dc.identifier10.1016/j.jchromb.2016.10.006
dc.identifier.issn15700232
dc.identifier.urihttp://hdl.handle.net/11615/77432
dc.description.abstractThe development and approbation of new, automated UHPLC-DAD method for the quantification of 25-hydroxyvitamin D3/D2 (25OH-D3/D2) metabolites in plasma/serum for the evaluation of patient's vitamin D status are presented. The method was developed on the Ultimate 3000 UHPLC dual gradient system supplied with the on-line SPE-concentration column coupled through six port switching valve to analytical column. This configuration and materials selected enable large volume sample injection (500 μL) and on-line sample preconcentration, clean up and subsequent selective metabolites transfer onto the analytical column. The new method abrogates main conventional time consuming and error source off-line steps of analysis and thus simplifies analysis. The large volume injection increases the sensitivity of instrumental analysis by about ten-fold on-line pre-concentration of metabolites. The instrument response is linear (R > 0.99) in the investigated concentration range 10–100 ng mL−1 which covers all the possible vitamin D status from serious deficiency (<12 ng mL−1) to excess. The method detection limits (S/N = 3) are LOD (25OH-D3) = 0.94 ng mL−1 and LOD (25OH-D2) = 2.4 ng mL−1. The method performance was assessed with the use of certified reference samples and perfect agreement between certified and measured values is demonstrated. The method was applied to human samples previously analyzed for total vitamin D by Competitive Protein-binding assay and findings of the two methods are compared. © 2016 Elsevier B.V.en
dc.language.isoenen
dc.sourceJournal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciencesen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85001799503&doi=10.1016%2fj.jchromb.2016.10.006&partnerID=40&md5=7e25f31effb9850a01b0d3b8228e947b
dc.subjectBiochemistryen
dc.subjectBiomoleculesen
dc.subjectMetabolitesen
dc.subjectPhase separationen
dc.subjectInstrumental analysisen
dc.subjectLarge volume injectionen
dc.subjectLarge-volume sample injectionen
dc.subjectMethod detection limitsen
dc.subjectOn-line preconcentrationen
dc.subjectOn-line sample preconcentrationen
dc.subjectOn-line solid phase extractionen
dc.subjectVitamin-Den
dc.subjectVitaminsen
dc.subject25 hydroxyergocalciferolen
dc.subjectcalcifediolen
dc.subjectdrug metaboliteen
dc.subject25 hydroxyergocalciferolen
dc.subjectcalcifediolen
dc.subjectArticleen
dc.subjectassayen
dc.subjectautomationen
dc.subjectcontrolled studyen
dc.subjecthumanen
dc.subjectinjectionen
dc.subjectlimit of detectionen
dc.subjectplasmaen
dc.subjectpriority journalen
dc.subjectprotein bindingen
dc.subjectserumen
dc.subjectsolid phase extractionen
dc.subjectswitching valveen
dc.subjectultra performance liquid chromatographyen
dc.subjectblooden
dc.subjectchemistryen
dc.subjecthigh performance liquid chromatographyen
dc.subjectisolation and purificationen
dc.subjectlimit of detectionen
dc.subjectproceduresen
dc.subjectreproducibilityen
dc.subjectsolid phase extractionen
dc.subjectstatistical modelen
dc.subject25-Hydroxyvitamin D 2en
dc.subjectCalcifediolen
dc.subjectChromatography, High Pressure Liquiden
dc.subjectHumansen
dc.subjectLimit of Detectionen
dc.subjectLinear Modelsen
dc.subjectReproducibility of Resultsen
dc.subjectSolid Phase Extractionen
dc.subjectElsevier B.V.en
dc.titleOn-line SPE sample treatment as a tool for method automatization and detection limits reduction: Quantification of 25-hydroxyvitamin D3/D2en
dc.typejournalArticleen


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