Analysis of new psychoactive substances in oral fluids by means of microextraction by packed sorbent followed by ultra-high-performance liquid chromatography-tandem mass spectrometry

被引:49
作者
Rocchi, Rachele [1 ]
Simeoni, Maria Chiara [1 ]
Montesano, Camilla [2 ]
Vannutelli, Gabriele [2 ]
Curini, Roberta [2 ]
Sergi, Manuel [1 ]
Compagnone, Dario [1 ]
机构
[1] Univ Teramo, Fac Biosci & Technol Food Agr & Environm, Teramo, Italy
[2] Sapienza Univ Rome, Dept Chem, I-00185 Rome, Italy
关键词
MEPS; new psychoactive substances; oral fluid; UHPLC-MS; MS; SYNTHETIC CANNABINOIDS; QUANTITATIVE MEASUREMENT; ALTERNATIVE SPECIMENS; FORENSIC TOXICOLOGY; ILLICIT DRUGS; GC-MS; METABOLITES; SALIVA; ABUSE; QUANTIFICATION;
D O I
10.1002/dta.2330
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In recent years, new drugs, commonly known as new psychoactive substances (NPS), appeared on the market, which include, among others, synthetic cannabinoids, cathinones, and tryptamine analogs of psilocin. The aim of this work was to develop and validate a new method for simultaneous screening and quantification of 31 NPS in oral fluid by ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). The chosen target analytes represented different chemical and toxicological NPS classes, such as synthetic cathinones, piperazines, phenethylamines, synthetic cannabinoids, and their metabolites. The procedure involved a rapid sample preparation based on protein precipitation followed by clean-up utilizing microextraction by packed sorbent (MEPS); the quantitative analysis was performed by UHPLC-MS/MS. The MEPS clean-up, regardless of non-quantitative recoveries for some analytes, provided an effective removal of interfering compounds, as demonstrated by reduced matrix effects found at different concentrations for all the analytes. The validation protocol, based on SWGTOX guidelines, demonstrated the suitability of the proposed method for quantitative analysis: linearity range ranged over 3 or 4 orders of magnitude; precision and accuracy tests gave RSD% values below 25%, and accuracy ranged from 85.9% to 107%, accomplishing SWGTOX requirements. Limits of detection (LODs) ranged between 0.005 ng/mL and 0.850 ng/mL and limits of quantification (LOQs) from 0.015 to 2.600 ng/mL.
引用
收藏
页码:865 / 873
页数:9
相关论文
共 41 条
[1]   Quantitative Measurement of XLR11 and UR-144 in Oral Fluid by LC-MS-MS [J].
Amaratunga, Piyadarsha ;
Thomas, Christopher ;
Lemberg, Bridget Lorenz ;
Lemberg, Dave .
JOURNAL OF ANALYTICAL TOXICOLOGY, 2014, 38 (06) :315-321
[2]   Quantitative Measurement of Synthetic Cathinones in Oral Fluid [J].
Amaratunga, Piyadarsha ;
Lemberg, Bridget Lorenz ;
Lemberg, Dave .
JOURNAL OF ANALYTICAL TOXICOLOGY, 2013, 37 (09) :622-628
[4]   Simultaneous Screening and Quantification of 29 Drugs of Abuse in Oral Fluid by Solid-Phase Extraction and Ultraperformance LC-MS/MS [J].
Badawi, Nora ;
Simonsen, Kirsten Wiese ;
Steentoft, Anni ;
Bernhoft, Inger Marie ;
Linnet, Kristian .
CLINICAL CHEMISTRY, 2009, 55 (11) :2004-2018
[5]   The incidence of drugs of impairment in oral fluid from random roadside testing [J].
Chu, Mark ;
Gerostamoulos, Dimitri ;
Beyer, Jochen ;
Rodda, Luke ;
Boorman, Martin ;
Drummer, Olaf H. .
FORENSIC SCIENCE INTERNATIONAL, 2012, 215 (1-3) :28-31
[6]   Determination of drugs of abuse and their metabolites in human plasma by liquid chromatography-mass spectrometry -: An application to 156 road fatalities [J].
Concheiro, M ;
de Castro, A ;
Quintela, O ;
López-Rivadulla, M ;
Cruz, A .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2006, 832 (01) :81-89
[7]   Determination of illicit and medicinal drugs and their metabolites in oral fluid and preserved oral fluid by liquid chromatography-tandem mass spectrometry [J].
Concheiro, Marta ;
de Castro, Ana ;
Quintela, Oscar ;
Cruz, Angelines ;
Lopez-Rivadulla, Manuel .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2008, 391 (06) :2329-2338
[8]   Synthetic Cannabinoids in Oral Fluid [J].
Coulter, Cynthia ;
Garnier, Margaux ;
Moore, Christine .
JOURNAL OF ANALYTICAL TOXICOLOGY, 2011, 35 (07) :424-430
[9]   Liquid chromatography tandem mass spectrometry determination of selected synthetic cathinones and two piperazines in oral fluid. Cross reactivity study with an on-site immunoassay device [J].
de Castro, Ana ;
Lendoiro, Elena ;
Fernandez-Vega, Hadriana ;
Steinmeyer, Stefan ;
Lopez-Rivadulla, Manuel ;
Cruz, Angelines .
JOURNAL OF CHROMATOGRAPHY A, 2014, 1374 :93-101
[10]   Determination of pharmaceutical and illicit drugs in oral fluid by ultra-high performance liquid chromatography-tandem mass spectrometry [J].
Di Corcia, D. ;
Lisi, S. ;
Pirro, V. ;
Gerace, E. ;
Salomone, A. ;
Vincenti, M. .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2013, 927 :133-141