Accurate and simple determination of oxcarbazepine in human plasma and urine samples using switchable-hydrophilicity solvent in GC-MS.
Sezin ErarpatSüleyman BodurMerve Fırat AyyıldızÖmer Tahir GünkaraFatih Ahmet ErulaşDotse Selali ChormeyFatma TurakTürkan Börklü BudakSezgin BakırderePublished in: Biomedical chromatography : BMC (2020)
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.
Keyphrases
- solid phase extraction
- ionic liquid
- gas chromatography mass spectrometry
- molecularly imprinted
- liquid chromatography tandem mass spectrometry
- high performance liquid chromatography
- carbon dioxide
- liquid chromatography
- simultaneous determination
- tandem mass spectrometry
- gas chromatography
- mass spectrometry
- ms ms
- solar cells
- gold nanoparticles