首页> 外文期刊>Journal of Analytical Toxicology >Simultaneous determination of eight underivatized amphetamines in hair by high-performance liquid chromatography-atmospheric pressure chemical ionization mass spectrometry (HPLC-APCI-MS).
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Simultaneous determination of eight underivatized amphetamines in hair by high-performance liquid chromatography-atmospheric pressure chemical ionization mass spectrometry (HPLC-APCI-MS).

机译:高效液相色谱-常压化学电离质谱(HPLC-APCI-MS)同时测定头发中的八种未衍生苯丙胺。

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摘要

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.
机译:这项研究的目的是开发,优化和验证分析程序,以确定一组八种苯丙胺,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),亚甲基二氧苯丙胺(MDA),亚甲基二氧甲基苯丙胺(MDMA)和亚甲基二氧乙基苯丙胺(MDEA)在头发中。碱(1M NaOH)消化后,用1-氯丁烷萃取目标物质,并用高效液相色谱-常压化学电离质谱法(LC-APCI-MS)进行衍生化分析。通过流动注射分析,优化了APCI-MS参数,如碎裂器和毛细管电压,电晕电流,干燥气体温度和流速,蒸发器温度和雾化器气体压力。使用研究药物的质子化分子离子的选定离子监测进行定量,并将其氘代类似物用作内标。 MA,MDA,MDMA和MDEA的检出限为0.05 ng / mg; EP和AMP为0.10 ng / mg; MTC和PMA为0.20 ng / mg。对于所有药物,从0到20 ng / mg均观察到线性响应。该方法用于测定从排毒和美沙酮治疗的患者中获得的93种真实头发样品中的苯丙胺含量,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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