Determination of amphetamine-type stimulants in oral fluid by solid-phase microextraction and gas chromatography-mass spectrometry

被引:42
|
作者
Souza, Daniele Z. [1 ,2 ]
Boehl, Paula O. [2 ]
Comiran, Eloisa [2 ]
Mariotti, Kristiane C. [2 ]
Pechansky, Flavio [3 ]
Duarte, Paulina C. A. V. [4 ]
De Boni, Raquel [3 ]
Froehlich, Pedro E. [2 ]
Limberger, Renata P. [2 ]
机构
[1] Dept Policia Fed Rio Grande Sul, Setor Tecn Cient, BR-90160093 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Programa Posgrad Ciencias Farmaceut, Fac Farm, BR-90610000 Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, CPAD, Hosp Clin Porto Alegre, BR-90035903 Porto Alegre, RS, Brazil
[4] Esplanada Minist, Secretaria Nacl Polit Drogas SENAD, BR-70050907 Brasilia, DF, Brazil
关键词
Amphetamine; Methamphetamine; Diethylpropion; Fenproporex; Methylphenidate; Oral fluid; INJURED DRIVERS; TRUCK DRIVERS; DRUG-USE; METHAMPHETAMINE; DERIVATIZATION; PREVALENCE; URINE; ABUSE; SALIVA; VALIDATION;
D O I
10.1016/j.aca.2011.04.014
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method for the simultaneous identification and quantification of amphetamine (AMP), methamphetamine (MET), fenproporex (FEN), diethylpropion (DIE) and methylphenidate (MPH) in oral fluid collected with Quantisal (TM) device has been developed and validated. Thereunto, in-matrix propylchloroformate derivatization followed by direct immersion solid-phase microextraction and gas chromatography-mass spectrometry were employed. Deuterium labeled AMP was used as internal standard for all the stimulants and analysis was performed using the selected ion monitoring mode. The detector response was linear for the studied drugs in the concentration range of 2-256 ng mL(-1) (neat oral fluid), except for FEN, whereas the linear range was 4-256 ng mL(-1). The detection limits were 0.5 ng mL(-1) (MET), 1 ng mL(-1) (MPH) and 2 ng mL(-1) (DIE, AMP, FEN), respectively. Accuracy of quality control samples remained within 98.2-111.9% of the target concentrations, while precision has not exceeded 15% of the relative standard deviation. Recoveries with Quantisal (TM) device ranged from 77.2% to 112.1%. Also, the goodness-of-fit concerning the ordinary least squares model in the statistical inference of data has been tested through residual plotting and ANOVA. The validated method can be easily automated and then used for screening and confirmation of amphetamine-type stimulants in drivers' oral fluid. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:67 / 76
页数:10
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