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高效液相色谱-大气压化学电离质谱法(HPLC-APCI-MS)同时测定毛发中8种未衍生化苯丙胺类药物

Simultaneous determination of eight underivatized amphetamines in hair by high-performance liquid chromatography-atmospheric pressure chemical ionization mass spectrometry (HPLC-APCI-MS).

作者信息

Stanaszek Roman, Piekoszewski Wojciech

机构信息

Institute of Forensic Research, ul. Westerplatte 9, 31-033 Cracow, Poland.

出版信息

J Anal Toxicol. 2004 Mar;28(2):77-85. doi: 10.1093/jat/28.2.77.

DOI:10.1093/jat/28.2.77
PMID:15068560
Abstract

The aim of this study was to develop, optimize, and validate an analytical procedure to determine a group of eight amphetamines, amphetamine (AMP), ephedrine (EP), methcathinone (MTC), paramethoxyamphetamine (PMA), methamphetamine (MA), methylenedioxyamphetamine (MDA), methylenedioxymethamphetamine (MDMA), and methylenedioxyethylamphetamine (MDEA), in hair. The target substances were extracted with 1-chlorobutane after alkaline (1M NaOH) digestion and analyzed underivatized with high-performance liquid chromatography-atmospheric pressure chemical ionization mass spectrometry (LC-APCI-MS). APCI-MS parameters such as fragmentor and capillary voltage, corona current, drying gas temperature and flow rate, vaporizer temperature, and nebulizer gas pressure were optimized with the application of flow injection analysis. Quantitation was performed using selected ion monitoring of protonated molecular ions of the studied drugs, and their deuterated analogues were used as internal standards. The limits of detection were 0.05 ng/mg for MA, MDA, MDMA, and MDEA; 0.10 ng/mg for EP and AMP; and 0.20 ng/mg for MTC and PMA. A linear response was observed for all drugs from 0 to 20 ng/mg. The method was applied to the determination of amphetamines in 93 authentic hair samples obtained from detoxification and methadone treatment patients, revealing the following concentrations: 0.17-17.28 ng/mg (EP), 0.52-2.08 ng/mg (MTC), 0.15-62.52 ng/mg (AMP), 0.10-16.52 ng/mg (MA), 0.10-0.88 ng/mg (MDMA), and 0.10-0.16 ng/mg (MDEA). MDA and PMA were never detected.

摘要

本研究的目的是开发、优化并验证一种分析方法,用于测定毛发中一组八种苯丙胺类物质,即苯丙胺(AMP)、麻黄碱(EP)、甲卡西酮(MTC)、对甲氧基苯丙胺(PMA)、甲基苯丙胺(MA)、亚甲二氧基苯丙胺(MDA)、亚甲二氧基甲基苯丙胺(MDMA)和亚甲二氧基乙基苯丙胺(MDEA)。目标物质在碱性(1M氢氧化钠)消化后用1-氯丁烷萃取,并用高效液相色谱-大气压化学电离质谱法(LC-APCI-MS)进行未衍生化分析。通过流动注射分析对APCI-MS参数(如碎裂器和毛细管电压、电晕电流、干燥气温度和流速、蒸发器温度和雾化器气压)进行了优化。使用所研究药物的质子化分子离子的选择离子监测进行定量,其氘代类似物用作内标。MA、MDA、MDMA和MDEA的检测限为0.05 ng/mg;EP和AMP为0.10 ng/mg;MTC和PMA为0.20 ng/mg。在0至20 ng/mg范围内,所有药物均呈现线性响应。该方法应用于测定从戒毒和美沙酮治疗患者处获得的93份真实毛发样本中的苯丙胺类物质,结果显示以下浓度:0.17 - 17.28 ng/mg(EP)、0.52 - 2.08 ng/mg(MTC)、0.15 - 62.52 ng/mg(AMP)、0.10 - 16.52 ng/mg(MA)、0.10 - 0.88 ng/mg(MDMA)和0.10 - 0.16 ng/mg(MDEA)。从未检测到MDA和PMA。

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