Your browser doesn't support javascript.
loading
Accurate and simple determination of oxcarbazepine in human plasma and urine samples using switchable-hydrophilicity solvent in GC-MS.
Erarpat, Sezin; Bodur, Süleyman; Ayyildiz, Merve Firat; Günkara, Ömer Tahir; Erulas, Fatih; Chormey, Dotse Selali; Turak, Fatma; Budak, Türkan Börklü; Bakirdere, Sezgin.
Affiliation
  • Erarpat S; Yildiz Technical University, Faculty of Art and Science, Chemistry Department, Istanbul, Turkey.
  • Bodur S; Yildiz Technical University, Faculty of Art and Science, Chemistry Department, Istanbul, Turkey.
  • Ayyildiz MF; Yildiz Technical University, Faculty of Art and Science, Chemistry Department, Istanbul, Turkey.
  • Günkara ÖT; Yildiz Technical University, Faculty of Art and Science, Chemistry Department, Istanbul, Turkey.
  • Erulas F; Siirt University, Faculty of Education, Department of Science Education, Siirt, Turkey.
  • Chormey DS; Yildiz Technical University, Faculty of Art and Science, Chemistry Department, Istanbul, Turkey.
  • Turak F; Yildiz Technical University, Faculty of Art and Science, Chemistry Department, Istanbul, Turkey.
  • Budak TB; Yildiz Technical University, Faculty of Art and Science, Chemistry Department, Istanbul, Turkey.
  • Bakirdere S; Yildiz Technical University, Faculty of Art and Science, Chemistry Department, Istanbul, Turkey.
Biomed Chromatogr ; 34(10): e4915, 2020 Oct.
Article in En | MEDLINE | ID: mdl-32529647
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 protonating N,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 µg/kg was obtained for the analyte. Limit of detection and quantitation values were found to be 6.2 and 21 µg/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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxcarbazepine / Gas Chromatography-Mass Spectrometry Type of study: Prognostic_studies Limits: Humans Language: En Journal: Biomed Chromatogr Year: 2020 Document type: Article Affiliation country: Turkey

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxcarbazepine / Gas Chromatography-Mass Spectrometry Type of study: Prognostic_studies Limits: Humans Language: En Journal: Biomed Chromatogr Year: 2020 Document type: Article Affiliation country: Turkey