Isoherranen N, Roeder M, Soback S, Yagen B, Schurig V, Bialer M
Department of Pharmaceutics, The Hebrew University of Jerusalem, Israel.
J Chromatogr B Biomed Sci Appl. 2000 Aug 18;745(2):325-32. doi: 10.1016/s0378-4347(00)00293-0.
A gas chromatographic-mass spectrometric method was developed for the enantioselective analysis of levetiracetam and its enantiomer (R)-alpha-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 microM 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)-alpha-ethyl-2-oxo-pyrrolidine acetamide in a dog.
建立了一种气相色谱 - 质谱法,用于对犬血浆和尿液中左乙拉西坦及其对映体(R)-α-乙基-2-氧代吡咯烷乙酰胺进行对映体选择性分析。采用固相萃取程序,然后在手性环糊精毛细管柱上对映体进行气相色谱分离,并使用离子阱质谱进行检测。使用串联质谱进一步研究了对映体的碎裂模式。为进行定量分析,从对映体中选择了三个单离子,以便在检测中进行选择离子监测。血浆样品的校准曲线在1 microM至2 mM范围内呈线性,尿液样品的校准曲线在0.5 mM至38 mM范围内呈线性。在血浆和尿液样品中,以相对标准偏差表示的日间精密度在所有浓度下均约为10%。选择离子监测质谱法适用于生物样品中宽浓度范围的左乙拉西坦及其对映体的定量分析。该方法已成功应用于犬体内左乙拉西坦和(R)-α-乙基-2-氧代吡咯烷乙酰胺的药代动力学研究。