Analysis of phenylpiperazine-like stimulants in human hair as trimethylsilyl derivatives by gas chromatography-mass spectrometry

被引:37
作者
Barroso, M. [1 ]
Costa, S. [1 ]
Dias, M. [1 ]
Vieira, D. N. [2 ]
Queiroz, J. A. [3 ]
Lopez-Rivadulla, M. [4 ]
机构
[1] Inst Nacl Med Legal Delegacao Sul, P-1150219 Lisbon, Portugal
[2] Inst Nacl Med Legal, P-3000213 Coimbra, Portugal
[3] Univ Beira Interior, Ctr Invest Ciencias Saude, P-6201506 Covilha, Portugal
[4] Inst Univ Med Legal, Santiago De Compostela 15782, Spain
关键词
Piperazines; Hair; GC/MS; DRUG N-BENZYLPIPERAZINE; LC-MS-MS; DESIGNER DRUGS; TOXICOLOGICAL DETECTION; ACTIVE METABOLITES; GC-MS; URINE; PIPERAZINE; ABUSE; TRAZODONE;
D O I
10.1016/j.chroma.2010.08.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple and sensitive procedure, using p-tolylpiperazine (pTP) as internal standard (IS), has been developed and validated for the qualitative and quantitative analysis of 1-(3-trifuoromethylphenyl)piperazine (TFMPP), 1-(3-chlorophenyl)piperazine (mCPP) and 1-(4-methoxyphenyl)piperazine (MeOPP) in hair. Drug extraction was performed by incubation with 1 M sodium hydroxide at 50 degrees C for 40 min, and the extracts were cleaned up using mixed-mode solid-phase extraction. The analytes were derivatized with N-methyl-N-(trimethylsilyl) trifluoroacetamide with 5% trimethylchlorosilane and analysed by gas chromatography-mass spectrometry in the selected ion monitoring mode. The method was linear from 0.05 (lower limit of quantitation) to 4 ng mg(-1), with correlation coefficients higher than 0.99 for all the compounds. Intra- and interday precision and accuracy were in conformity with the criteria normally accepted in bioanalytical method validation, and the sample cleanup step presented a mean efficiency higher than 90% for all the analytes. Due to its simplicity and speed, this method can be successfully applied in the screening and quantitation of these compounds in hair samples, and is suitable for application in forensic toxicology routine analysis. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:6274 / 6280
页数:7
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