Yayın: Accurate and simple determination of oxcarbazepine in human plasma and urine samples using switchable-hydrophilicity solvent in GC-MS
| dc.contributor.author | Erarpat, Sezin | |
| dc.contributor.author | Bodur, Suleyman | |
| dc.contributor.author | Ayyildiz, Merve Firat | |
| dc.contributor.author | Gunkara, Omer Tahir | |
| dc.contributor.author | Erulas, Fatih | |
| dc.contributor.author | Chormey, Dotse Selali | |
| dc.contributor.author | Turak, Fatma | |
| dc.contributor.author | Budak, Turkan Borklu | |
| dc.contributor.author | Bakirdere, Sezgin | |
| dc.date.accessioned | 2026-06-27T14:29:27Z | |
| dc.date.issued | 2020 | |
| dc.description.abstract | This 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.sponsorship | Yildiz Technical University Scientific Research Project [FBA2019-3530] | |
| dc.description.uri | https://doi.org/10.1002/bmc.4915 | |
| dc.identifier.doi | 10.1002/bmc.4915 | |
| dc.identifier.eissn | 1099-0801 | |
| dc.identifier.issn | 0269-3879 | |
| dc.identifier.issue | 10 | |
| dc.identifier.pubmed | 32529647 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14981/61214 | |
| dc.identifier.volume | 34 | |
| dc.identifier.wos | 000548918900001 | |
| dc.language.iso | eng | |
| dc.publisher | WILEY | |
| dc.relation.ispartof | BIOMEDICAL CHROMATOGRAPHY | |
| dc.subject | gas chromatography-mass spectrometry | |
| dc.subject | human plasma | |
| dc.subject | oxcarbazepine | |
| dc.subject | switchable hydrophilicity solvent | |
| dc.subject | urine | |
| dc.subject | LIQUID-LIQUID MICROEXTRACTION | |
| dc.subject | 6 ANTIEPILEPTIC DRUGS | |
| dc.subject | PHASE MICROEXTRACTION | |
| dc.subject | SIMULTANEOUS QUANTIFICATION | |
| dc.subject | ELECTROSPRAY-IONIZATION | |
| dc.subject | MASS-SPECTROMETRY | |
| dc.subject | HPLC-UV | |
| dc.subject | CARBAMAZEPINE | |
| dc.subject | CHROMATOGRAPHY | |
| dc.subject | METABOLITES | |
| dc.subject | Biochemistry & Molecular Biology | |
| dc.subject | Chemistry | |
| dc.subject | Pharmacology & Pharmacy | |
| dc.title | Accurate and simple determination of oxcarbazepine in human plasma and urine samples using switchable-hydrophilicity solvent in GC-MS | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.import.source | WOS |