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.
引用
收藏
页数:12
相关论文
共 50 条
  • [21] A Bioanalytical Method for Quantification of Thioredoxins in Bacillus anthracis by Digestion with Immobilized Pepsin and LC-MS/MS and On-line LC/LC-MS/MS
    Saleh, Aljona
    Edlund, Per-Olof
    Gustafsson, Tomas N.
    Sahlin, Margareta
    Sjoberg, Britt-Marie
    Granelli, Ingrid
    CHROMATOGRAPHIA, 2016, 79 (7-8) : 383 - 393
  • [22] An LC-MS assay for the screening of cardiovascular medications in human samples
    Dias, Eduardo
    Hachey, Brian
    McNaughton, Candace
    Nian, Hui
    Yu, Chang
    Straka, Brittany
    Brown, Nancy J.
    Caprioli, Richard M.
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2013, 937 : 44 - 53
  • [23] Detection and quantification of selected cannabinoids in oral fluid samples by protein precipitation and LC-MS/MS
    Antunes, Monica
    Simoes, Susana
    Fonseca, Suzana
    Franco, Joao
    Gallardo, Eugenia
    Barroso, Mario
    FORENSIC SCIENCE INTERNATIONAL, 2024, 363
  • [24] Validation of an LC-MS/MS Method for the Quantification of 13 Designer Benzodiazepines in Blood
    Mei, Victoria
    Concheiro, Marta
    Pardi, Justine
    Cooper, Gail
    JOURNAL OF ANALYTICAL TOXICOLOGY, 2019, 43 (09) : 688 - 695
  • [25] LC-MS/MS screening method for designer amphetamines, tryptamines, and piperazines in serum
    Wohlfarth, Ariane
    Weinmann, Wolfgang
    Dresen, Sebastian
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2010, 396 (07) : 2403 - 2414
  • [26] HILIC LC-MS/MS method for the quantification of cefepime, imipenem and meropenem
    Rehm, Sophia
    Rentsch, Katharina M.
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2020, 186
  • [27] A multi-analyte LC-MS/MS method for screening and quantification of nitrosamines in sartans
    Chang, Shu-Han
    Chang, Ching-Chia
    Wang, Li-Jing
    Chen, Wei-Ching
    Fan, Shu-Yu
    Zang, Chi-Zong
    Hsu, Ya-Hui
    Lin, Mei-Chih
    Tseng, Su-Hsiang
    Wang, Der-Yuan
    JOURNAL OF FOOD AND DRUG ANALYSIS, 2020, 28 (02) : 98 - 107
  • [28] A Sensitive LC-MS/MS Assay for the Quantification of Methadone and its Metabolites in Dried Blood Spots: Comparison With Plasma
    Davari, Baharak
    Kotecha, Nidhi
    Clavijo, Claudia F.
    Thomas, James J.
    Rzasa-Lynn, Rachael
    Galinkin, Jeffrey L.
    Christians, Uwe
    Sempio, Cristina
    THERAPEUTIC DRUG MONITORING, 2020, 42 (01) : 118 - 128
  • [29] Quantification of AICAR-ribotide concentrations in red blood cells by means of LC-MS/MS
    Thomas, Andreas
    Vogel, Matthias
    Piper, Thomas
    Krug, Oliver
    Beuck, Simon
    Schanzer, Wilhelm
    Thevis, Mario
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2013, 405 (30) : 9703 - 9709
  • [30] LC-MS/MS for protein and peptide quantification in clinical chemistry
    Rauh, Manfred
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2012, 883 : 59 - 67