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SHR Neuro Krebs Kardio Lipid Stoffw Microb
Leis, HJ; Schütz, H; Windischhofer, W.
Quantitative determination of methylphenidate in plasma by gas chromatography negative ion chemical ionisation mass spectrometry using o-(pentafluorobenzyloxycarbonyl)-benzoyl derivatives.
Anal Bioanal Chem. 2011; 400(8):2663-2670
Doi: 10.1007/s00216-011-5048-6
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PubMed
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- Führende Autor*innen der Med Uni Graz
- Leis Hans-Joerg
- Co-Autor*innen der Med Uni Graz
- Windischhofer Werner
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- Abstract:
- The use of a novel electrophoric derivatisation reagent, o-(pentafluorobenzyloxycarbonyl)-benzoyl chloride, for the quantitative determination of methylphenidate in plasma is described. The drug can be quantitatively measured down to 72 pg/mL plasma using only 250 μL of sample due to the extraordinary sensitivity of the derivatives under negative ion chemical ionisation mass spectrometry. Plasma samples were made alkaline with carbonate buffer and treated with extraction solvent n-hexane and reagent solution for 30 min, which, after concentration, was measured by GC-NICI-MS. The method is rapid as extraction and derivatisation occur in one single step. A stable isotope-labelled internal standard was used and its synthesis described. Full validation data are given to demonstrate the usefulness of the assay, including specificity, linearity, accuracy and precision, long-term stability, short-term stability, freeze-thaw stability, stock solution stability, autosampler stability, aliquot analysis, robustness, matrix effect, and prospective analytical batch size accuracy. The method has been successfully applied to pharmacokinetic profiling of the drug after oral application.
- Find related publications in this database (using NLM MeSH Indexing)
- Benzoates - chemical synthesis
- Gas Chromatography-Mass Spectrometry -
- Humans -
- Methylphenidate - blood
- Molecular Structure -
- Stereoisomerism -
- Find related publications in this database (Keywords)
- Methylphenidate
- GC-MS
- Negative ion chemical ionisation
- PBBCl
- Derivatisation