Yayın:
Accurate and simple determination of oxcarbazepine in human plasma and urine samples using switchable-hydrophilicity solvent in GC-MS

dc.contributor.authorErarpat, Sezin
dc.contributor.authorBodur, Suleyman
dc.contributor.authorAyyildiz, Merve Firat
dc.contributor.authorGunkara, Omer Tahir
dc.contributor.authorErulas, Fatih
dc.contributor.authorChormey, Dotse Selali
dc.contributor.authorTurak, Fatma
dc.contributor.authorBudak, Turkan Borklu
dc.contributor.authorBakirdere, Sezgin
dc.date.accessioned2026-06-27T14:29:27Z
dc.date.issued2020
dc.description.abstractThis work presents a sensitive and rapid analytical method for the determination of oxcarbazepine in human plasma and urine samples. A vortex-assisted switchable hydrophilicity solvent-based liquid phase microextraction (VA-SHS-LPME) was used to preconcentrate oxcarbazepine from the samples before the determination by gas chromatography mass spectrometry. The switchable hydrophilicity solvent was synthesized by protonatingN,N-dimethylbenzylamine with carbon dioxide to make it totally miscible with an equivalent volume of water. Parameters of the VA-SHS-LPME method including volume of switchable hydrophilicity solvent, concentration/volume of sodium hydroxide and vortex period were systematically optimized. Under the optimum conditions, good linearity ranging from 27.03 to 353.47 mu g/kg was obtained for the analyte. Limit of detection and quantitation values were found to be 6.2 and 21 mu g/kg (mass base), respectively. The relative standard deviation was calculated as 6.9% for six replicate measurements of the lowest concentration of the calibration plot. Satisfactory recovery results were calculated in the range of 97-100% for human plasma and urine samples spiked at five different concentrations.en
dc.description.sponsorshipYildiz Technical University Scientific Research Project [FBA2019-3530]
dc.description.urihttps://doi.org/10.1002/bmc.4915
dc.identifier.doi10.1002/bmc.4915
dc.identifier.eissn1099-0801
dc.identifier.issn0269-3879
dc.identifier.issue10
dc.identifier.pubmed32529647
dc.identifier.urihttps://hdl.handle.net/20.500.14981/61214
dc.identifier.volume34
dc.identifier.wos000548918900001
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofBIOMEDICAL CHROMATOGRAPHY
dc.subjectgas chromatography-mass spectrometry
dc.subjecthuman plasma
dc.subjectoxcarbazepine
dc.subjectswitchable hydrophilicity solvent
dc.subjecturine
dc.subjectLIQUID-LIQUID MICROEXTRACTION
dc.subject6 ANTIEPILEPTIC DRUGS
dc.subjectPHASE MICROEXTRACTION
dc.subjectSIMULTANEOUS QUANTIFICATION
dc.subjectELECTROSPRAY-IONIZATION
dc.subjectMASS-SPECTROMETRY
dc.subjectHPLC-UV
dc.subjectCARBAMAZEPINE
dc.subjectCHROMATOGRAPHY
dc.subjectMETABOLITES
dc.subjectBiochemistry & Molecular Biology
dc.subjectChemistry
dc.subjectPharmacology & Pharmacy
dc.titleAccurate and simple determination of oxcarbazepine in human plasma and urine samples using switchable-hydrophilicity solvent in GC-MS
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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