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Simultaneous quantitative determination of amphetamines, ketamine, opiates and metabolites in human hair by gas chromatography/mass spectrometry

机译:气相色谱/质谱法同时定量测定人发中的苯丙胺,氯胺酮,鸦片制剂和代谢产物

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A gas chromatography/mass spectrometry (GC/MS) method was developed and validated for the determination of common drugs of abuse in Asia. The method was able to simultaneously quantify amphetamines (amphetamine; AP, methamphetamine; MA, methylenedioxy amphetamine; MDA, methylenedioxymeth mphetamine; MDMA, methylenedioxy ethylamphetamine; MDEA), ketamine (ketamine; K, norketamine; NK), and opiates (morphine; MOR, codeine; COD, 6-acetylmorphine; 6-AM) in human hair. Hair samples (25mg) were washed, cut, and incubated overnight at 25 degrees C in methanol/trifluoroacetic acid (methanol/TFA). The samples were extracted by solid-phase extraction (SPE), derivatized using heptafluorobutyric acid anhydride (HFBA) at 70 degrees C for 30 min, and the derivatives were analyzed by electron ionization (ED GC/MS in selected ion monitoring mode. Confirmation was accomplished by comparing retention times and the relative abundances of selected ions with those of standards. Deuterated analogs of the analytes were Used as internal standards for quantification. Calibration curves for ten analytes were established in the concentration range 0.1-10 ng/mg with high correlation coefficients (r(2) > 0.999). The intra-day and inter-day precisions were within 12.1% and 15.8%, respectively. The intra-day and inter-day accuracies were between -8.7% and 10.7%, and between -5.9% and 13.8%, respectively. The limit of detection (LOD) and limit of quantification (LOQ) obtained were 0.03 and 0.05 ng/mg for AP, MA, MDA, MDMA and MDEA; 0.05 and 0.08 ng/mg for K, NK, MOR and COD; and 0.08 and 0.1 ng/mg for 6-AM. The recoveries were above 88.6% for all the compounds, except K and NK which were in the range of 71.7-72.7%. Eight hair samples from known polydrug abusers were examined by this method. These results show that the method is suitable for broad-spectrum drug testing in a single hair specimen. Copyright (C) 2008 John Wiley & Sons, Ltd.
机译:气相色谱/质谱法(GC / MS)的开发和验证已用于确定亚洲常见的滥用药物。该方法能够同时定量安非他命(安非他命; AP,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,亚甲二氧基乙基苯丙胺; MDEA),氯胺酮(氯胺酮; K,诺酮胺; NK)和鸦片剂(吗啡; MOR ,可待因;化学需氧量,6-乙酰吗啡; 6-AM)。将头发样品(25mg)洗涤,切割,并在25℃下在甲醇/三氟乙酸(甲醇/ TFA)中孵育过夜。样品通过固相萃取(SPE)萃取,在70摄氏度下使用七氟丁酸酐(HFBA)衍生30分钟,然后在选定的离子监测模式下通过电子电离(ED GC / MS)分析衍生物。通过比较所选离子的保留时间和相对丰度与标准品的相对丰度,使用氘化的分析物类似物作为内标进行定量,建立了十种分析物在0.1-10 ng / mg浓度范围内的校正曲线,并具有高度相关性系数(r(2)> 0.999)。日内和日间精度分别在12.1%和15.8%之内;日内和日间精度在-8.7%和10.7%之间,以及- AP,MA,MDA,MDMA和MDEA的检测限(LOD)和定量限(LOQ)分别为5.9%和13.8 ng / mg; K,0.05和0.08 ng / mg NK,MOR和COD;对于0.08和0.1 ng / mg 6点。所有化合物的回收率均高于88.6%,但K和NK的回收率在71.7-72.7%范围内。用这种方法检查了八名来自已知滥用毒品者的头发样本。这些结果表明,该方法适用于在单个头发样本中进行广谱药物测试。版权所有(C)2008 John Wiley&Sons,Ltd.

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