TY - JOUR
T1 - Enantioselective analysis of levetiracetam and its enantiomer R-α- ethyl-2-oxo-pyrrolidine acetamide using gas chromatography and ion trap mass spectrometric detection
AU - Isoherranen, Nina
AU - Roeder, Michael
AU - Soback, Stefan
AU - Yagen, Boris
AU - Schurig, Volker
AU - Bialer, Meir
PY - 2000/8/18
Y1 - 2000/8/18
N2 - 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.
AB - 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.
KW - Enantiomer separation
KW - Levetiracetam
KW - R-(α)-ethyl-2-oxo-pyrrolidine acetamide
UR - http://www.scopus.com/inward/record.url?scp=0034683005&partnerID=8YFLogxK
U2 - 10.1016/S0378-4347(00)00293-0
DO - 10.1016/S0378-4347(00)00293-0
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C2 - 11043751
AN - SCOPUS:0034683005
SN - 1387-2273
VL - 745
SP - 325
EP - 332
JO - Journal of Chromatography B: Biomedical Sciences and Applications
JF - Journal of Chromatography B: Biomedical Sciences and Applications
IS - 2
ER -