High throughput identification and quantification of 16 antipsychotics and 8 major metabolites in serum using ultra-high performance liquid chromatography-tandem mass spectrometry

被引:69
作者
Patteet, Lisbeth [1 ,2 ]
Maudens, Kristof E. [1 ]
Sabbe, Bernard [3 ,4 ]
Morrens, Manuel [2 ,5 ]
De Doncker, Mireille [2 ]
Neels, Hugo [1 ,2 ]
机构
[1] Univ Antwerp, Toxicol Ctr, B-2610 Antwerp, Belgium
[2] ZNA Stuivenberg, Lab TDM & Toxicol, B-2060 Antwerp, Belgium
[3] Univ Antwerp, Fac Med, CAPRI, B-2610 Antwerp, Belgium
[4] Psychiat Ctr Sint Norbertushuis, B-2570 Duffel, Belgium
[5] Psychiat Hosp Broeders Alexianen, B-2530 Boechout, Belgium
关键词
Antipsychotics; UHPLC-MS/MS; Neuroleptics; Therapeutic drug monitoring; Mass spectrometry; HEMOLYZED WHOLE-BLOOD; HUMAN PLASMA; PSYCHOTROPIC-DRUGS; QUANTITATIVE-DETERMINATION; ATYPICAL ANTIPSYCHOTICS; CONSENSUS GUIDELINES; ORAL FLUID; LC-MS/MS; IONIZATION; OLANZAPINE;
D O I
10.1016/j.cca.2013.11.024
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Therapeutic drug monitoring of antipsychotics is important for optimizing therapy, explaining adverse effects, non-response or poor compliance. We developed a UHPLC-MS/MS method for quantification of 16 commonly used and recently marketed antipsychotics and 8 metabolites in serum. Methods: After liquid-liquid extraction using methyl tert-butyl ether, analysis was performed on an Agilent Technologies 1290 Infinity LC system coupled with an Agilent Technologies 6460 Triple Quadrupole MS. Separation with a C18 column and gradient elution at 0.5 mL/min resulted in a 6-min run-time. Detection was performed in dynamic MRM, monitoring 3 ion transitions per compound. Isotope labeled internal standards were used for every compound, except for bromperidol and levosulpiride. Results: Mean recovery was 86.8%. Matrix effects were -18.4 to +9.1%. Accuracy ranged between 91.3 and 107.0% at low, medium and high concentrations and between 76.2 and 113.9% at LLOQ. Within-run precision was <15% (CV), except for asenapine and hydroxy-iloperidone. Between-run precision was aberrant only for 7-hydroxy-N-desalkylquetiapine, asenapine and reduced haloperidol. No interferences were found. No problems of instability were observed, even for olanzapine. The method was successfully applied on patient samples. Conclusions: The liquid-liquid extraction and UHPLC-MS/MS technique allows robust target screening and quantification of 23 antipsychotics and metabolites. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:51 / 58
页数:8
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