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高效液相色谱-串联质谱法同时分析唾液中的丁丙诺啡、美沙酮、可卡因、阿片类药物、尼古丁及其代谢物。

High-throughput simultaneous analysis of buprenorphine, methadone, cocaine, opiates, nicotine, and metabolites in oral fluid by liquid chromatography tandem mass spectrometry.

机构信息

Servicio de Toxicología Forense, Dpto. Anatomía Patológica y Ciencias Forenses, Facultad de Medicina, Universidad de Santiago de Compostela, C/San Francisco s/n, 15782, Santiago de Compostela (A Coruña), Spain.

出版信息

Anal Bioanal Chem. 2010 Sep;398(2):915-24. doi: 10.1007/s00216-010-3903-5. Epub 2010 Jul 23.

Abstract

A method for simultaneous determination of buprenorphine (BUP), norbuprenorphine (NBUP), methadone, 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP), cocaine, benzoylecgonine (BE), ecgonine methyl ester (EME), anhydroecgonine methyl ester (AEME), morphine, codeine, 6-acetylmorphine (6AM), heroin, 6-acetylcodeine (6AC), nicotine, cotinine, and trans-3'-hydroxycotinine (OH-cotinine) by liquid chromatography tandem mass spectrometry in oral fluid (OF) was developed and extensively validated. Acetonitrile (800 μL) and OF (250 μL) were added to a 96-well Isolute-PPT+protein precipitation plate. Reverse-phase separation was achieved in 16 min and quantification was performed by multiple reaction monitoring. The assay was linear from 0.5 or 1 to 500 μg/L. Intraday, interday, and total imprecision were less than 13% (n = 20), analytical recovery was 92-114% (n = 20), extraction efficiencies were more than 77% (n = 5), and process efficiencies were more than 45% (n = 5). Although ion suppression was detected for EME, cocaine, morphine, 6AC, and heroin (less than 56%) and enhancement was detected for BE and nicotine (less than 316%), deuterated internal standards compensated for these effects. The method was sensitive (limit of detection 0.2-0.8 μg/L) and specific (no interferences) except that 3-hydroxy-4-methoxyamphetamine interfered with AEME. No carryover was detected, and all analytes were stable for 24 h at 22 °C, for 72 h at 4 °C, and after three freeze-thaw cycles, except cocaine, 6AC, and heroin (22-97% loss). The method was applied to 41 OF specimens collected throughout pregnancy with a Salivette® OF collection device from an opioid-dependent BUP-maintained pregnant woman. BUP ranged from 0 to 7,400 μg/L, NBUP from 0 to 71 μg/L, methadone from 0 to 3 μg/L, nicotine from 32 to 5,020 μg/L, cotinine from 125 to 508 μg/L, OH-cotinine from 11 to 51 μg/L, cocaine from 0 to 419 μg/L, BE from 0 to 351 μg/L, EME from 0 to 286 μg/L, AEME from 0 to 7 μg/L, morphine from 0 to 22 μg/L, codeine from 0 to 1 μg/L, 6AM from 0 to 4 μg/L, and heroin from 0 to 2 μg/L. All specimens tested negative for EDDP and 6AC. This method permits a fast and simultaneous quantification of 16 drugs and metabolites in OF, with good selectivity and sensitivity.

摘要

一种同时测定唾液中丁丙诺啡(BUP)、去甲丁丙诺啡(NBUP)、美沙酮、2-亚乙基-1,5-二甲基-3,3-二苯基吡咯烷(EDDP)、可卡因、苯甲酰古柯碱(BE)、可可碱甲酯(EME)、脱水可可碱甲酯(AEME)、吗啡、可待因、6-乙酰吗啡(6AM)、海洛因、6-乙酰可待因(6AC)、尼古丁、可替宁和反式-3'-羟基可替宁(OH-可替宁)的液相色谱串联质谱法已被开发并得到广泛验证。向 96 孔 Isolute-PPT+蛋白沉淀板中加入乙腈(800 μL)和唾液(250 μL)。在 16 分钟内实现反相分离,并通过多反应监测进行定量。该测定法的线性范围为 0.5 或 1 至 500 μg/L。日内、日间和总精密度均小于 13%(n=20),分析回收率为 92-114%(n=20),提取效率大于 77%(n=5),过程效率大于 45%(n=5)。尽管 EME、可卡因、吗啡、6AC 和海洛因(小于 56%)存在离子抑制,BE 和尼古丁(小于 316%)存在增强,但氘代内标可补偿这些影响。该方法灵敏度高(检测限为 0.2-0.8 μg/L)且特异性好(无干扰),但 3-羟基-4-甲氧基苯丙胺会干扰 AEME 的测定。未检出残留,所有分析物在 22°C 下稳定 24 小时,4°C 下稳定 72 小时,经过三个冻融循环后,除可卡因、6AC 和海洛因(22-97%损失)外,均稳定。该方法应用于从一名丁丙诺啡维持的阿片类药物依赖孕妇的 Salivette®唾液收集装置中收集的 41 份唾液样本。BUP 浓度范围为 0 至 7400 μg/L,NBUP 浓度范围为 0 至 71 μg/L,美沙酮浓度范围为 0 至 3 μg/L,尼古丁浓度范围为 32 至 5020 μg/L,可替宁浓度范围为 125 至 508 μg/L,OH-可替宁浓度范围为 11 至 51 μg/L,可卡因浓度范围为 0 至 419 μg/L,BE 浓度范围为 0 至 351 μg/L,EME 浓度范围为 0 至 286 μg/L,AEME 浓度范围为 0 至 7 μg/L,吗啡浓度范围为 0 至 22 μg/L,可待因浓度范围为 0 至 1 μg/L,6AM 浓度范围为 0 至 4 μg/L,海洛因浓度范围为 0 至 2 μg/L。所有样本均未检出 EDDP 和 6AC。该方法允许快速、同时定量分析唾液中的 16 种药物和代谢物,具有良好的选择性和灵敏度。

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