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
  • [11] A novel screening method for 64 new psychoactive substances and 5 amphetamines in blood by LC-MS/MS and application to real cases
    Vaiano, Fabio
    Busardo, Francesco P.
    Palumbo, Diego
    Kyriakou, Chrystalla
    Fioravanti, Alessia
    Catalani, Valeria
    Mari, Francesco
    Bertol, Elisabetta
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2016, 129 : 441 - 449
  • [12] Development and validation of an LC-MS/MS method for the quantification of ephedrines in urine
    Deventer, K.
    Pozo, O. J.
    Van Eenoo, P.
    Delbeke, F. T.
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2009, 877 (04): : 369 - 374
  • [13] An LC-MS/MS Method Development and Validation for the Quantification of Abametapir in Plasma Samples
    Sankar, Palakollu D. S.
    Panigrahi, Naresh
    SEPARATION SCIENCE PLUS, 2025, 8 (01):
  • [14] A simple LC-MS/MS method for the simultaneous quantification of endocannabinoids in biological samples
    Bobrich, Maria
    Schwarz, Rico
    Ramer, Robert
    Borchert, Philipp
    Hinz, Burkhard
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2020, 1161
  • [15] Quantification of the Immunosuppressant Tacrolimus on Dried Blood Spots Using LC-MS/MS
    Shokati, Touraj
    Bodenberger, Nicholas
    Gadpaille, Holly
    Schniedewind, Bjoern
    Vinks, Alexander A.
    Jiang, Wenlei
    Alloway, Rita R.
    Christians, Uwe
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2015, (105):
  • [16] Quantification of ribociclib in dried blood spots by LC-MS/MS : Method development and clinical validation
    Braal, C. Louwrens
    Lam, Mei H.
    Rienks, Tineke
    van Tilborg, Claudia J.
    Heuts, Wendy
    Heijns, Joan B.
    Bos, Monique E. M. M.
    Mathijssen, Ron H. J.
    de Bruijn, Peter
    Koolen, Stijn L. W.
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2021, 201
  • [17] LC-MS/MS method for the quantification of cortisol of hepatocellular carcinoma
    Zhou, Zijing
    Li, Xiaoshuang
    Yin, Shengjun
    Zhang, Zhiyuan
    Li, Xiaoyue
    Miao, Xiaojie
    Cheng, Haixu
    Lou, Yaqing
    Tu, Pengfei
    Lu, Yingyuan
    Zhang, Guoliang
    BIOMEDICAL CHROMATOGRAPHY, 2024, 38 (04)
  • [18] A rapid LC-MS/MS Method for the Quantification of Cyclosporine A in Rabbit Whole Blood and Plasma
    Huang, Yi
    Xu, Zhi-sheng
    Zheng, Shuang-li
    Hou, Yao
    LATIN AMERICAN JOURNAL OF PHARMACY, 2013, 32 (07): : 1035 - 1041
  • [19] Fast determination of amphetamine-type stimulants and synthetic cathinones in whole blood samples using protein precipitation and LC-MS/MS
    Cunha, Ricardo Leal
    Lima Oliveira, Celinalva da Silva
    de Oliveira, Aline Lima
    Maldaner, Adriano Otavio
    Pereira, Pedro Afonso P.
    MICROCHEMICAL JOURNAL, 2021, 163
  • [20] Detection and quantification of vitamins in microliter volumes of biological samples by LC-MS for clinical screening
    Khaksari, Maryam
    Mazzoleni, Lynn R.
    Ruan, Chunhai
    Song, Peng
    Hershey, Neil D.
    Kennedy, Robert T.
    Burns, Mark A.
    Minerick, Adrienne R.
    AICHE JOURNAL, 2018, 64 (10) : 3709 - 3718