Department of Analytical Chemistry, Faculty of Pharmacy, University of the Basque Country, Vitoria-Gasteiz, Spain.
Forensic Sci Int. 2012 Jun 10;219(1-3):172-8. doi: 10.1016/j.forsciint.2012.01.002. Epub 2012 Jan 20.
A quantitative LC-MS/MS method has been developed for the simultaneous determination of 17 antipsychotic drugs in human postmortem brain tissue. Sample preparation was performed using Hybrid Solid Phase Extraction-Precipitation technology for the removal of endogenous protein and phospholipid interferences. The chromatographic separation was performed for 16 min on a C8 column, which used a gradient elution of formate ammonium and acetonitrile, and a flow rate gradient. Triple quadrupole mass spectrometry was employed to generate tandem mass spectrometric (MS/MS) data of the target analytes to select the ion m/z signals. Quantitation of the analytes was performed by operating in the dynamic multiple reaction monitoring (dMRM) mode using an electrospray ionization interface. Calibration curves prepared in the spiked brain tissue were linear in the range 20-8000 ng/g (r(2)>0.993) for all drugs (except olanzapine). Within- and between-day coefficients of variation were lower than 25% for all drugs at the LOQ. The LOQ in the matrix ranged between 2 ng/g and 80 ng/g. The method was successfully applied to the unequivocal identification and accurate quantification of antipsychotic drugs in human postmortem brain tissues: therefore, this method can be used in forensic investigations.
已开发出一种用于同时测定人死后脑组织中 17 种抗精神病药物的定量 LC-MS/MS 方法。采用混合固相萃取-沉淀技术进行样品前处理,以去除内源性蛋白质和磷脂干扰。在 C8 柱上进行 16 分钟的色谱分离,采用甲酸铵和乙腈的梯度洗脱和流速梯度。三重四极杆质谱用于生成目标分析物的串联质谱(MS/MS)数据,以选择离子 m/z 信号。采用电喷雾电离接口以动态多重反应监测(dMRM)模式进行定量分析。在加标脑组织中制备的校准曲线在所有药物(奥氮平除外)的 20-8000ng/g 范围内呈线性(r(2)>0.993)。所有药物在 LOQ 时的日内和日间变异系数均低于 25%。基质中的 LOQ 在 2ng/g 至 80ng/g 之间。该方法成功应用于人死后脑组织中抗精神病药物的明确鉴定和准确定量:因此,该方法可用于法医调查。