Quantitative Method Validation for the Analysis of 27 Antidepressants and Metabolites in Plasma With Ultraperformance Liquid Chromatography-Tandem Mass Spectrometry

被引:43
|
作者
Ramirez Fernandez, Maria del Mar [1 ]
Wille, Sarah M. R. [1 ]
Samyn, Nele [1 ]
机构
[1] Natl Inst Criminalist & Criminol, Fed Publ Serv Justice, B-1120 Brussels, Belgium
关键词
UPLC-MS/MS; plasma; antidepressants; NEW-GENERATION ANTIDEPRESSANTS; SOLID-PHASE EXTRACTION; LC-MS/MS METHOD; ACTIVE METABOLITES; WHOLE-BLOOD; MS; QUANTIFICATION; NORTRIPTYLINE; BIOANALYSIS; CITALOPRAM;
D O I
10.1097/FTD.0b013e31823bf0fd
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
A fast and selective ultraperformance liquid chromatographic- tandem mass spectrometric method was developed and validated for the simultaneous quantification of amitriptyline, citalopram, clomipramine, desipramine, desmethylcitalopram, desmethylclomipramine, desmethyldosulepin, desmethyldoxepin, desmethylfluoxetine, desmethylvenlafaxine, didesmethylcitalopram, dosulepin, doxepin, duloxetine, fluoxetine, fluvoxamine, imipramine, maprotiline, mianserin, mirtazapine, moclobemide, nortriptyline, paroxetine, reboxetine, sertraline, trazodone, and venlafaxine in 100 mu L of plasma. After liquid-liquid extraction with 1-chlorobutane, analytes were separated on a BEH (Ethylene Bridged Hybrid) C18 analytical column with gradient elution. The compounds were ionized and detected over 7-minute analysis time by electrospray ionization tandem mass spectrometry with multiple reaction monitoring. Limits of quantification and limits of detection ranged from 2.5 to 10 ng/mL and 0.2 to 10 ng/mL, respectively. Intra-and interassay imprecision were lower than 15% for all the compounds except for mirtazapine, moclobemide, and desmethylclomipramine [relative standard deviation (RSD), < 20%], and the bias of the assay was lower than 15% for all the compounds except for fluvoxamine (bias < 20.5%), evaluated with 5 commercial quality control and 3 "in-house'' quality control. The extraction was found to be reproducible (RSD, 16%) (except for duloxetine RSD 21.9%) and with recoveries varying from 59% to 86%. Furthermore, the stability studies demonstrated that the processed samples were stable in the autosampler for 24 hours for all the compounds. The method was successfully applied to the analysis of authentic samples from forensic toxicology cases and external quality control assays from the Society of Toxicology and Forensic Chemistry (GTFCh). The method was completely validated and can be of interest to clinical and forensic laboratories.
引用
收藏
页码:11 / 24
页数:14
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