High performance liquid chromatography-high resolution mass spectrometry and micropulverized extraction for the quantification of amphetamines, cocaine, opioids, benzodiazepines, antidepressants and hallucinogens in 2.5 mg hair samples

被引:65
作者
Favretto, Donata [1 ]
Vogliardi, Susanna [1 ]
Stocchero, Giulia [2 ]
Nalesso, Alessandro [1 ]
Tucci, Marianna [1 ]
Ferrara, Santo Davide [1 ]
机构
[1] Univ Padua, Dept Publ Hlth & Environm Med, I-35121 Padua, Italy
[2] Univ Hosp Padova, I-35121 Padua, Italy
关键词
HPLC-HRMS; Orbitrap; Hair; Drugs of abuse; Pharmaceuticals; Pulverization; Extraction; SOLID-PHASE MICROEXTRACTION; HIGH-THROUGHPUT ANALYSIS; DRUGS; OPIATES; BENZOYLECGONINE; ABUSE; METABOLITES; COCAETHYLENE; METHAMPHETAMINE; SPECIMENS;
D O I
10.1016/j.chroma.2011.07.050
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A high performance liquid chromatography-high resolution mass spectrometry (HPLC-HRMS) method for simultaneous screening and quantification of 28 drugs was developed and validated for 2.5 mg hair samples. Target drugs and their metabolites included amphetamines, cocaine, opioids, benzodiazepines, antidepressants, and hallucinogens. After decontamination, hair samples were extracted with 200 mu L of a mixture of water: acetonitrile:1 M trifluoroacetic acid (80:10:10, v/v) using a 5 min simultaneous pulverization/extraction step. The extracts were analysed by HPLC-HRMS in an Orbitrap at a nominal resolution of 60,000, with concomitant in source collisional experiments (in source CID). Gradient elution on an Atlantis T3 column resolved 28 target compounds and 5 internal standards. Total chromatographic run time was 26 min. Calibration was achieved by linear regression analysis utilizing six calibration points; R-2 ranged from 0.9964 to 0.9999, the limits of quantification were 0.1 ng/mg for 8 compounds, 0.2 ng/mg for 16 compounds and 0.5 ng/mg for 4 compounds: mean relative errors from -21% to +23% were obtained; relative standard deviation, used to estimate repeatability and intermediate reproducibility at three concentrations, was always less than 20%. Process efficiency and recoveries for all analytes were better than 65 and 73%, respectively, at any concentration. The method was applied to hair samples from forensic investigations that contained a broad assortment of drugs of abuse and pharmaceuticals. The use of concomitant HRMS full scan and CID afforded the possibility of retrospective analysis for discovering untargeted drugs. (C) 2011 Published by Elsevier B.V.
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页码:6583 / 6595
页数:13
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