Mochizuki Akira, Nakazawa Hiroko, Adachi Noboru, Takekawa Kenichi, Shojo Hideki
Forensic Science Laboratory, Yamanashi Prefectural Police Headquarters, 312-4 Kubonakajima, Isawa, Fuefuki, Yamanashi 406-0036 Japan.
2Department of Legal Medicine, Graduate Faculty of Interdisciplinary Research, University of Yamanashi, 1110 Shimokato, Chuo, Yamanashi 409-3898 Japan.
Forensic Toxicol. 2018;36(1):81-87. doi: 10.1007/s11419-017-0384-7. Epub 2017 Sep 12.
We encountered a curious case in which two male subjects self-administered mepirapim plus acetyl fentanyl by different routes, i.e., intravenously and by inhalation. We have thus established a detailed procedure for quantification of mepirapim and acetyl fentanyl in whole blood and urine specimens using gas chromatography (GC)-tandem mass spectrometry (MS/MS).
The GC-MS/MS method was validated for linearity, extraction recovery, accuracy, and precision. Liquid chromatography-MS/MS was also used for identification of the target compounds.
Good linearity and reproducibility were achieved in the range of 20-1000 ng/g for both target compounds in both matrices. The concentrations of mepirapim in heart whole blood, femoral vein whole blood, and urine of the deceased individual with administration by intravenous injection were 593, 567, and 527 ng/g, respectively; those of acetyl fentanyl were 155, 125, and 126 ng/g, respectively. The mepirapim and acetyl fentanyl concentrations in the urine specimen of the surviving individual who had administered them by inhalation were 4900 and 570 ng/g, respectively.
To our knowledge, with the exception of a brief mention of a mepirapim concentration in a serum sample in emergency medicine, there are no reported data on the identification and quantification of mepirapim in biological samples. Mepirapim is a new synthetic cannabinoid. The concentration profiles of unchanged mepirapim in whole blood and urine were quite different and unique. A detailed clarification of such uniqueness is under way in our laboratory.
我们遇到了一个奇特的案例,两名男性受试者通过不同途径自行服用了甲哌吡嗪加乙酰芬太尼,即静脉注射和吸入。因此,我们建立了一种详细的程序,使用气相色谱(GC)-串联质谱(MS/MS)对全血和尿液样本中的甲哌吡嗪和乙酰芬太尼进行定量。
对GC-MS/MS方法的线性、提取回收率、准确性和精密度进行了验证。液相色谱-MS/MS也用于目标化合物的鉴定。
两种基质中两种目标化合物在20-1000 ng/g范围内均具有良好的线性和重现性。静脉注射给药的死者心脏全血、股静脉全血和尿液中甲哌吡嗪的浓度分别为593、567和527 ng/g;乙酰芬太尼的浓度分别为155、125和126 ng/g。通过吸入服用甲哌吡嗪和乙酰芬太尼的幸存者尿液样本中,甲哌吡嗪和乙酰芬太尼的浓度分别为4900和570 ng/g。
据我们所知,除了急诊医学中血清样本中甲哌吡嗪浓度的简短提及外,尚无关于生物样本中甲哌吡嗪鉴定和定量的报道数据。甲哌吡嗪是一种新型合成大麻素。全血和尿液中未变化的甲哌吡嗪浓度分布截然不同且独特。我们实验室正在对这种独特性进行详细阐释。