Enantioselective analysis of levetiracetam and its enantiomer R-α- ethyl-2-oxo-pyrrolidine acetamide using gas chromatography and ion trap mass spectrometric detection

Nina Isoherranen, Michael Roeder, Stefan Soback, Boris Yagen, Volker Schurig, Meir Bialer*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

56 Scopus citations

Abstract

A gas chromatographic-mass spectrometric method was developed for the enantioselective analysis of levetiracetam and its enantiomer (R)-α-ethyl-2- oxo-pyrrolidine acetamide in dog plasma and urine. A solid-phase extraction procedure was followed by gas chromatographic separation of the enantiomers on a chiral cyclodextrin capillary column and detection using ion trap mass spectrometry. The fragmentation pattern of the enantiomers was further investigated using tandem mass spectrometry. For quantitative analysis three single ions were selected from the enantiomers, enabling selected ion monitoring in detection. The calibration curves were linear from 1 μM to 2 mM for plasma samples and from 0.5 mM to 38 mM for urine samples. In plasma and urine samples the inter-day precision, expressed as relative standard deviation was around 10% in all concentrations. Selected ion monitoring mass spectrometry is suitable for quantitative analysis of a wide concentration range of levetiracetam and its enantiomer in biological samples. The method was successfully applied to a pharmacokinetic study of levetiracetam and (R)- α-ethyl-2-oxo-pyrrolidine acetamide in a dog. (C) 2000 Elsevier Science B.V.

Original languageEnglish
Pages (from-to)325-332
Number of pages8
JournalJournal of Chromatography B: Biomedical Sciences and Applications
Volume745
Issue number2
DOIs
StatePublished - 18 Aug 2000

Keywords

  • Enantiomer separation
  • Levetiracetam
  • R-(α)-ethyl-2-oxo-pyrrolidine acetamide

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