A broad-spectrum LC-MS/MS method for screening and quantification of 100 analytes in clinical and autopsy blood samples

被引:0
|
作者
Florou, Dimitra [1 ,2 ,3 ]
Di Rago, Mathew [2 ,3 ]
Orfanidis, Amvrosios [1 ,4 ]
Gerostamoulos, Dimitri
Boumba, Vassiliki A. [1 ,4 ]
机构
[1] Univ Ioannina, Fac Med, Sch Hlth Sci, Dept Forens Med & Toxicol, Univ Campus, Ioannina 45500, Greece
[2] Victorian Inst Forens Med Toxicol, 65 Kavanagh St, Melbourne, Vic 3006, Australia
[3] Monash Univ, Dept Forens Med, Melbourne, Vic 3006, Australia
[4] Univ Hosp Ioannina, Ioannina 45110, Greece
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2024年 / 1247卷
关键词
Blood; Drugs; LC-MS/MS; NPS; Forensic toxicology; PSYCHOACTIVE SUBSTANCES; WHOLE-BLOOD; MASS-SPECTROMETRY; DRUGS; EXTRACTION; SERUM;
D O I
10.1016/j.jchromb.2024.124323
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Liquid chromatography coupled with mass spectrometry (LC-MS) has been tremendously used for screening purposes in forensic toxicology, because of their great adaptability and reasonable time/resource consumption. Herein, a fully validated method based on liquid-liquid extraction (LLE) in human whole blood, by a multiple reaction monitoring (MRM) analysis through LC-MS/MS, is described. The proposed method simultaneously detects 100 analytes (plus three deuterated internal standard compounds) belonging to many different classes, including drugs of abuse, prescription and over-the-counter drugs commonly involved in poisoning and medical malpractice cases in our territory, as well as certain new psychoactive substances (NPS) and toxic substances potentially associated with adverse effects. The optimised LLE employs one extraction step of 200 mu L blood using 0.1 M HCl methyl-tert-butyl-ether (MTBE) (acidified with concentrated HCl) proved to be suitable for the extraction of basic and neutral substances; as a reconstitution solvent a mixture of 88:12v/v, 0.1 % formic acid in 10 mM aqueous ammonium acetate, pH 3.5: 0.1 % formic acid in acetonitrile was used, yielding satisfactory recoveries for all analytes. The method was sensitive, showing low LOD/ LOQ for all substances ranging from 0.01 to 5/ 0.05-20 ng/mL, respectively. Linearity ranged between 0.05-500 ng/mL (R-2 = 0.9811-0.9995), and the inter- and intra-day precisions ranged between 3-15 % and 7-18 %, respectively. Accuracy was evaluated in terms of percentage recovery, lying within acceptable range. The matrix effect expressed as ion suppression/enhancement of each analyte was in the range +/- 25 % for all analytes. Post-preparative stability of analytes was higher than 85 %, while no carryover between runs was observed. The developed method has been successfully applied in routine toxicological analyses for the analysis of biological samples from clinical and autopsy cases.
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页数:12
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