Andersson Maria, Stephanson Nikolai, Ohman Inger, Terzuoli Tommy, Lindh Jonatan D, Beck Olof
Division of Clinical Pharmacology, Karolinska Institute and University Hospital, Stockholm, Sweden.
Drug Test Anal. 2014 Apr;6(4):317-24. doi: 10.1002/dta.1486. Epub 2013 May 29.
Opiates comprise a class of abused drugs that is of primary interest in clinical and forensic urine drug testing. Determination of heroin, codeine, or a multi-drug ingestion is complicated since both heroin and codeine can lead to urinary excretion of free and conjugated morphine. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) offers advantage over gas chromatography-mass spectrometry by simplifying sample preparation but increases the number of analytes. A method based on direct injection of five-fold diluted urine for confirmation of morphine, morphine-3-glucuronide, morphine-6-glucuronide, codeine, codeine-6-glucuronide and 6-acetylmorphine was validated using LC-MS/MS in positive electrospray mode monitoring two transitions using selected reaction monitoring. The method was applied for the analysis of 3155 unknown urine samples which were positive for opiates in immunochemical screening. A linear response was observed for all compounds in the calibration curves covering more than three orders of magnitude. Cut off was set to 2 ng/ml for 6-acetylmorphine and 150 ng/ml for the other analytes. 6-Acetylmorphine was found to be effective (sensitivity 82%) in detecting samples as heroin intake. Morphine-3-glucuronide and codeine-6-glucuronide was the predominant components of total morphine and codeine, 84% and 93%, respectively. The authors have validated a robust LC-MS/MS method for rapid qualitative and quantitative analysis of opiates in urine. 6-Acetylmorphine has been demonstrated as a sensitive and important parameter for a heroin intake. A possible interpretation strategy to conclude the source of detected analytes was proposed. The method might be further developed by reducing the number of analytes to morphine-3-glucuronide, codeine-6-glucuronide and 6-acetylmorphine without compromising test performance.
阿片类药物是一类在临床和法医尿液药物检测中备受关注的滥用药物。由于海洛因和可待因都会导致游离态和结合态吗啡经尿液排泄,因此测定海洛因、可待因或多种药物摄入情况较为复杂。液相色谱 - 串联质谱法(LC-MS/MS)相比气相色谱 - 质谱法具有优势,它简化了样品制备过程,但增加了分析物的数量。本文验证了一种基于直接进样五倍稀释尿液的方法,用于确证吗啡、吗啡 - 3 - 葡萄糖醛酸苷、吗啡 - 6 - 葡萄糖醛酸苷、可待因、可待因 - 6 - 葡萄糖醛酸苷和6 - 单乙酰吗啡,采用LC-MS/MS在正电喷雾模式下通过选择反应监测来监测两个跃迁。该方法应用于分析3155份在免疫化学筛查中阿片类药物呈阳性的未知尿液样本。在校准曲线中,所有化合物在超过三个数量级的范围内均呈现线性响应。6 - 单乙酰吗啡的截断值设定为2 ng/ml,其他分析物的截断值设定为150 ng/ml。结果发现6 - 单乙酰吗啡在检测海洛因摄入样本方面有效(灵敏度为82%)。吗啡 - 3 - 葡萄糖醛酸苷和可待因 - 6 - 葡萄糖醛酸苷分别是总吗啡和总可待因的主要成分,分别占84%和93%。作者验证了一种可靠的LC-MS/MS方法,用于尿液中阿片类药物的快速定性和定量分析。6 - 单乙酰吗啡已被证明是海洛因摄入的一个敏感且重要的参数。本文还提出了一种推断检测到的分析物来源的可能解释策略。该方法可通过减少分析物数量至吗啡 - 3 - 葡萄糖醛酸苷、可待因 - 6 - 葡萄糖醛酸苷和6 - 单乙酰吗啡,而不影响测试性能,从而进一步改进。