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一种用于同时定量汗液中吗啡、海洛因、可卡因及其代谢物的固相萃取气相色谱 - 质谱法的开发与验证

Development and validation of a solid-phase extraction gas chromatography-mass spectrometry method for the simultaneous quantification of methadone, heroin, cocaine and metabolites in sweat.

作者信息

Brunet Bertrand R, Barnes Allan J, Scheidweiler Karl B, Mura Patrick, Huestis Marilyn A

机构信息

INSERM E-0324, Université de Poitiers, Faculté de Médecine et Pharmacie, CHU de Poitiers, Rue de la Milétrie, BP 577, 86021, Poitiers, France.

出版信息

Anal Bioanal Chem. 2008 Sep;392(1-2):115-27. doi: 10.1007/s00216-008-2228-0. Epub 2008 Jul 8.

Abstract

A sensitive and specific method is presented to simultaneously quantify methadone, heroin, cocaine and metabolites in sweat. Drugs were eluted from sweat patches with sodium acetate buffer, followed by SPE and quantification by GC/MS with electron impact ionization and selected ion monitoring. Daily calibration for anhydroecgonine methyl ester, ecgonine methyl ester, cocaine, benzoylecgonine (BE), codeine, morphine, 6-acetylcodeine, 6-acetylmorphine (6AM), heroin (5-1000 ng/patch) and methadone (10-1000 ng/patch) achieved determination coefficients of >0.995, and calibrators quantified to within +/-20% of the target concentrations. Extended calibration curves (1000-10,000 ng/patch) were constructed for methadone, cocaine, BE and 6AM by modifying injection techniques. Within (N = 5) and between-run (N = 20) imprecisions were calculated at six control levels across the dynamic ranges with coefficients of variation of <6.5%. Accuracies at these concentrations were +/-11.9% of target. Heroin hydrolysis during specimen processing was <11%. This novel assay offers effective monitoring of drug exposure during drug treatment, workplace and criminal justice monitoring programs.

摘要

本文介绍了一种灵敏且特异的方法,可同时对汗液中的美沙酮、海洛因、可卡因及其代谢物进行定量分析。药物用醋酸钠缓冲液从汗液贴片上洗脱下来,随后进行固相萃取,并通过带有电子轰击电离和选择离子监测的气相色谱/质谱联用仪进行定量分析。对去甲芽子碱甲酯、芽子碱甲酯、可卡因、苯甲酰芽子碱(BE)、可待因、吗啡、6-乙酰可待因、6-乙酰吗啡(6AM)、海洛因(每贴片10 - 1000纳克)和美沙酮(每贴片10 - 1000纳克)进行每日校准,测定系数>0.995,校准物定量结果在目标浓度的±20%以内。通过改进进样技术构建了美沙酮、可卡因、BE和6AM的扩展校准曲线(每贴片1000 - 10000纳克)。在整个动态范围内的六个控制水平上计算批内(N = 5)和批间(N = 20)精密度,变异系数<6.5%。这些浓度下的准确度为目标值的±11.9%。样本处理过程中海洛因的水解率<11%。这种新方法为药物治疗、工作场所和刑事司法监测项目中的药物暴露监测提供了有效的手段。

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