• Title of article

    Fast quantification of ten psychotropic drugs and metabolites in human plasma by ultra-high performance liquid chromatography tandem mass spectrometry for therapeutic drug monitoring

  • Author/Authors

    Ansermot، نويسنده , , Nicolas and Brawand-Amey، نويسنده , , Marlyse and Kottelat، نويسنده , , Astrid and Eap، نويسنده , , Chin B. Eap، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2013
  • Pages
    13
  • From page
    160
  • To page
    172
  • Abstract
    A sensitive and selective ultra-high performance liquid chromatography (UHPLC) tandem mass spectrometry (MS/MS) method was developed for the fast quantification of ten psychotropic drugs and metabolites in human plasma for the needs of our laboratory (amisulpride, asenapine, desmethyl-mirtazapine, iloperidone, mirtazapine, norquetiapine, olanzapine, paliperidone, quetiapine and risperidone). Stable isotope-labeled internal standards were used for all analytes, to compensate for the global method variability, including extraction and ionization variations. Sample preparation was performed by generic protein precipitation with acetonitrile. Chromatographic separation was achieved in less than 3.0 min on an Acquity UPLC BEH Shield RP18 column (2.1 mm × 50 mm; 1.7 μm), using a gradient elution of 10 mM ammonium formate buffer pH 3.0 and acetonitrile at a flow rate of 0.4 ml/min. The compounds were quantified on a tandem quadrupole mass spectrometer operating in positive electrospray ionization mode, using multiple reaction monitoring. The method was fully validated according to the latest recommendations of international guidelines. Eight point calibration curves were used to cover a large concentration range 0.5–200 ng/ml for asenapine, desmethyl-mirtazapine, iloperidone, mirtazapine, olanzapine, paliperidone and risperidone, and 1–1500 ng/ml for amisulpride, norquetiapine and quetiapine. Good quantitative performances were achieved in terms of trueness (93.1–111.2%), repeatability (1.3–8.6%) and intermediate precision (1.8–11.5%). Internal standard-normalized matrix effects ranged between 95 and 105%, with a variability never exceeding 6%. The accuracy profiles (total error) were included in the acceptance limits of ±30% for biological samples. This method is therefore suitable for both therapeutic drug monitoring and pharmacokinetic studies.
  • Keywords
    Antidepressants , Protein precipitation , UHPLC–MS/MS , Method validation , therapeutic drug monitoring , Antipsychotics
  • Journal title
    Journal of Chromatography A
  • Serial Year
    2013
  • Journal title
    Journal of Chromatography A
  • Record number

    1518346