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用氯甲酸三氯乙酯衍生化后,通过气相色谱/质谱法测定血浆、尿液和毛发样本中的苯丙胺类药物和麻黄碱。

Gas chromatography/mass spectrometry determination of amphetamine-related drugs and ephedrines in plasma, urine and hair samples after derivatization with 2,2,2-trichloroethyl chloroformate.

作者信息

Frison Giampietro, Tedeschi Luciano, Favretto Donata, Reheman Aikebaier, Ferrara Santo Davide

机构信息

Forensic Toxicology and Antidoping, University Hospital of Padova, Via Falloppio 50, I-35121 Padova, Italy.

出版信息

Rapid Commun Mass Spectrom. 2005;19(7):919-27. doi: 10.1002/rcm.1873.

DOI:10.1002/rcm.1873
PMID:15747332
Abstract

A new analytical approach, based on derivatization with 2,2,2-trichloroethyl chloroformate and gas chromatography/mass spectrometry (GC/MS), was investigated for qualitative and quantitative analyses of a large range of amphetamine-related drugs and ephedrines in plasma, urine and hair samples. Sample preparation involved alkaline extraction of analytes from biological samples using Extrelut columns, after addition of the internal standard 3,4-methylenedioxypropylamphetamine (MDPA), and subsequent derivatization to produce 2,2,2-trichloroethylcarbamates. GC/MS analyses, in splitless mode using a slightly polar 30-m capillary column, were performed with quadrupole or ion trap instruments. MS acquisition modes were electron ionization (EI) in full-scan or selected ion monitoring (SIM) modes (quadrupole), and full-scan MS or MS/MS modes with chemical ionization (CI) conditions (ion trap). EI spectra of 2,2,2-trichloroethylcarbamates showed variably abundant molecular ions as well as abundant diagnostic fragment ions, both characterized by ion clusters reflecting the isotope distribution of three chlorine atoms in the derivatized molecules. CI spectra showed abundant protonated molecules. Quantitative studies using EI SIM conditions gave recoveries in the range 74-89%, linear response over ranges of 10-2000 ng/mL (plasma and urine) and 0.20-20 ng/mg (hair), with corresponding limits of detection in the ranges 2-5 ng/mL and 0.1-0.2 ng/mg. Potential applications (following full method validation) include clinical and forensic toxicology, as well as doping control.

摘要

研究了一种基于用氯甲酸-2,2,2-三氯乙酯衍生化和气相色谱/质谱联用(GC/MS)的新分析方法,用于定性和定量分析血浆、尿液和毛发样本中一系列与苯丙胺相关的药物和麻黄碱。样品制备包括在加入内标3,4-亚甲二氧基丙基苯丙胺(MDPA)后,使用硅藻土柱从生物样品中碱性萃取分析物,随后进行衍生化以生成2,2,2-三氯乙基氨基甲酸酯。使用略具极性的30米毛细管柱,在不分流模式下用四极杆或离子阱仪器进行GC/MS分析。质谱采集模式为全扫描或选择离子监测(SIM)模式(四极杆)下的电子电离(EI),以及化学电离(CI)条件下的全扫描质谱或质谱/质谱模式(离子阱)。2,2,2-三氯乙基氨基甲酸酯的EI谱显示出丰度各异的分子离子以及丰富的诊断性碎片离子,两者均以反映衍生化分子中三个氯原子同位素分布的离子簇为特征。CI谱显示出丰富的质子化分子。在EI SIM条件下进行的定量研究回收率在74 - 89%范围内,在10 - 2000 ng/mL(血浆和尿液)和0.20 - 20 ng/mg(毛发)范围内呈线性响应,相应的检测限在2 - 5 ng/mL和0.1 - 0.2 ng/mg范围内。(在完整方法验证之后)潜在应用包括临床和法医毒理学以及兴奋剂检测。

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