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Simultaneous determination of fluoxetine, venlafaxine, vortioxetine and their active metabolites in human plasma by LC-MS/MS using one-step sample preparation procedure.
Kertys, Martin; Krivosova, Michaela; Ondrejka, Igor; Hrtanek, Igor; Tonhajzerova, Ingrid; Mokry, Juraj.
Affiliation
  • Kertys M; Department of Pharmacology, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia; Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia. Electronic address: martin.kertys@uniba.sk.
  • Krivosova M; Department of Pharmacology, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia.
  • Ondrejka I; Clinic of Psychiatry, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia.
  • Hrtanek I; Clinic of Psychiatry, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia.
  • Tonhajzerova I; Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia; Department of Physiology, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia.
  • Mokry J; Department of Pharmacology, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia; Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia.
J Pharm Biomed Anal ; 181: 113098, 2020 Mar 20.
Article in En | MEDLINE | ID: mdl-31978643
ABSTRACT
The aim of antidepressant therapy is to induce remission and prevent relapses of major depressive disorder with minimum adverse effects during the treatment. Due to high variability in metabolism, therapeutic drug monitoring is recommended as a useful tool for individualisation of the therapy. For this purpose, we have developed simple and sensitive ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method for quantification of fluoxetine (FLX), venlafaxine (VEN), vortioxetine (VTX) and their active metabolites norfluoxetine (NFLX) and O-desmethylvenlafaxine (ODV). After one-step extraction procedure using OSTRO plate, analytes were separated by gradient elution on Acquity UPLC BEH C18 (50 × 2.1 mm, 1.7 µm) column with runtime 4.2 min. The detection was done on a triple quadrupole tandem mass spectrometer by multiple reaction monitoring (MRM) mode with transitions at m/z 310.23 → 148.20 for FLX, m/z 296.23 → 134.20 for NFLX, m/z 278.31 → 121.13 for VEN, m/z 264.31 → 107.14 for ODV and m/z 299.19 → 150.05 for VTX using a positive electrospray ionisation interface. The method was successfully validated according to the European Medicine Agency guideline for the selectivity, linearity and lower limit of detection, precision and accuracy, matrix effect, extraction recovery, carryover, dilution integrity and stability over a concentration range of 1-300 ng/mL for FLX, NFLX, VEN, ODV and 0.2-100 ng/mL VTX. Extraction recovery for each analyte was > 80 %, and no significant matrix effects were observed. The developed method was employed for quantification of antidepressants in clinical samples from patients treated with either FLX, VEN, or VTX.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Fluoxetine / Liquid-Liquid Extraction / Venlafaxine Hydrochloride / Vortioxetine Type of study: Guideline Limits: Adolescent / Adult / Aged / Child / Humans / Middle aged Language: En Journal: J Pharm Biomed Anal Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Fluoxetine / Liquid-Liquid Extraction / Venlafaxine Hydrochloride / Vortioxetine Type of study: Guideline Limits: Adolescent / Adult / Aged / Child / Humans / Middle aged Language: En Journal: J Pharm Biomed Anal Year: 2020 Document type: Article