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Rapid Simultaneous Determination of 14 Antidepressants and 13 Antipsychotics in Human Plasma by Using High-Performance Liquid Chromatography–Tandem Mass Spectrometry With Dynamic Multiple Reaction Monitoring and Its Application to Therapeutic Drug Monitoring

分析物 蛋白质沉淀 治疗药物监测 色谱法 串联质谱法 检出限 药代动力学 液相色谱-质谱法 质谱法 选择性反应监测 化学 药理学 医学
作者
Haiyan Lyu,Binbin Chen,Xiangzhen Xu,Chunyan Zhu,Chunling Ma,Yu Du,Farong Liu,Caisheng Wu
出处
期刊:Therapeutic Drug Monitoring [Ovid Technologies (Wolters Kluwer)]
卷期号:43 (4): 577-588 被引量:9
标识
DOI:10.1097/ftd.0000000000000839
摘要

Background: A comprehensive, stable, and efficient high-performance liquid chromatography–tandem mass spectrometry method was developed for rapidly analyzing 14 antidepressants and 13 antipsychotics in human plasma for routine clinical therapeutic drug monitoring. Methods: Simple protein precipitation was used for the pretreatment of plasma samples; dynamic multiple reaction monitoring was used to avoid the loss of sensitivity caused by numerous ion transitions. In all, 80 ion transitions of 40 compounds were quantitatively determined in 6 minutes. Results: The limit of detection for the 27 analytes was in the range of 0.1–30 ng/mL, and all calibration lines prepared using blank plasma were linear with a correlation coefficient of r 2 ≥ 0.99. The method was accurate and precise with acceptable intraday and interday precisions (coefficients of variation, ≤20% for a lower limit of quantification and ≤15% for other quality control samples) and an accuracy of 85.51%–114.77%. This analysis method has been completely validated and successfully used in routine clinical therapeutic drug monitoring for more than 9963 samples [including 488 samples having drug concentrations above the laboratory alert level (supra–alert-level samples)] at Xiamen Xianyue Hospital. Conclusions: This dynamic method is comprehensive (includes most antidepressants and antipsychotics listed in China), reliable (stably used for almost 2 years), and efficient (convenient sample processing and short run time) and provides a large amount of meaningful data for optimized pharmacotherapy. Our experimental data from the plasma concentrations of supra–alert-level samples could serve as a reference for the interpretation of the pharmacokinetics of patients with a high risk of toxicity or loss of tolerability.
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