Nirogi Ramakrishna, Bhyrapuneni Gopinadh, Kandikere Vishwottam, Mudigonda Koteshwara, Ajjala Devender, Mukkanti K
Pharmacokinetics and Drug Metabolism, Drug Discovery, Suven Life Sciences Ltd, Serene Chambers, Road 5, Avenue 7, Banjara Hills, Hyderabad 500034, India.
Biomed Chromatogr. 2008 Oct;22(10):1043-55. doi: 10.1002/bmc.1012.
A sensitive high-performance liquid chromatography-tandem mass spectrometry method was developed and validated for the quantification of quetiapine in rat plasma. Following liquid-liquid extraction, the analyte was separated using a gradient mobile phase on a reverse-phase column and analyzed by MS/MS in the multiple reaction monitoring mode using the respective [M + H]+ ions, m/z 384 to m/z 221 for quetiapine and m/z 327 to m/z 270 for the internal standard. The assay exhibited a linear dynamic range of 0.25-500 ng/mL for quetiapine in rat plasma. The lower limit of quantification was 0.25 ng/mL with a relative standard deviation of less than 7%. Acceptable precision and accuracy were obtained for concentrations over the standard curve range. The validated method was successfully used to analyze rat plasma samples for application in pre-clinical pharmacokinetic studies. This method in rodent plasma could be adapted for quetiapine assay in human plasma.
建立了一种灵敏的高效液相色谱 - 串联质谱法,并对其进行验证,用于定量大鼠血浆中的喹硫平。液 - 液萃取后,在反相柱上使用梯度流动相分离分析物,并在多反应监测模式下通过MS/MS使用各自的[M + H]+离子进行分析,喹硫平的m/z为384至m/z 221,内标的m/z为327至m/z 270。该测定法在大鼠血浆中喹硫平的线性动态范围为0.25 - 500 ng/mL。定量下限为0.25 ng/mL,相对标准偏差小于7%。在标准曲线范围内的浓度获得了可接受的精密度和准确度。经过验证的方法成功用于分析大鼠血浆样本,以应用于临床前药代动力学研究。这种在啮齿动物血浆中的方法可适用于人血浆中喹硫平的测定。