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Distinguishing Between Cyclopropylfentanyl and Crotonylfentanyl by Methods Commonly Available in the Forensic Laboratory

机译:通过法医实验室常用的方法区分环丙基芬太基和癸酰芬太基之间的方法

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Background: The opioid analgesic fentanyl and its analogues pose a major health concern due to its high potency and the increasing number of overdose deaths worldwide. The analogues of fentanyl may differ in potency, toxicity, and legal status, and it is therefore important to develop analytical methods for their correct identification. This can be challenging since many fentanyl analogues are structural isomers. Two fentanyl isomers that have been in the spotlight lately due to difficulties regarding separation and identification are cyclopropylfentanyl and crotonylfentanyl, which have been reported to display nearly identical fragmentation patterns and chromatographic behavior. Methods: Chromatographic separation of cyclopropylfentanyl and crotonylfentanyl by ultra-high-performance liquid chromatography was investigated using 3 different stationary phases (high strength silica T3, ethylsiloxane/silica hybrid C18 and Kinetex biphenyl) using gradient elution with a mobile phase consisting of 10 mM ammonium formate pH 3.1 and MeOH. Detection was performed by tandem mass spectrometry. In addition, the major metabolites of the 2 compounds formed on incubation with human liver microsomes were identified by ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry analysis. Results: Baseline separation of cyclopropylfentanyl and crotonylfentanyl was achieved on the ethylsiloxane/silica hybrid C18 column with retention times of 6.79 and 7.35 minutes, respectively. The major metabolites of the 2 analogues formed by human liver microsomes differed, with the main biotransformation being N-dealkyla-tion and carboxylation for cyclopropylfentanyl and crotonylfentanyl, respectively. We demonstrated the usefulness of the 2 approaches by unambiguously identifying cyclopropylfentanyl, as well as its metabolites, in 2 authentic postmortem blood samples. Conclusions: In this study, we successfully demonstrated that cyclopropylfentanyl and crotonylfentanyl can be distinguished by methods commonly available in forensic laboratories.
机译:背景:阿片类镇痛芬太尼及其类似物由于其高效力和越来越多的过量死亡而越来越多的效力。芬太尼的类似物可能效力,毒性和法律地位不同,因此为其正确识别产生分析方法是重要的。这可能是挑战性,因为许多芬太尼类似物是结构异构体。由于分离和鉴定的困难,最近一直在聚光灯中的两个芬太尼异构体是据报道的环丙基戊基壬基和癸酰芬太基,其据报道显示几乎相同的碎片模式和色谱行为。方法:使用3种不同的固定相(高强度硅T3,乙基硅氧烷/二氧化硅杂合C18和KINETEX BIPHENYL)研究了通过超高效液相色谱法使用超高效液相色谱法的色谱分离,使用梯度洗脱,其具有由10mM铵组成的流动相形成pH 3.1和MeOH。通过串联质谱法进行检测。此外,通过超高效液相色谱 - 四极杆飞行时间质谱分析鉴定在与人肝微粒体孵育中形成的2种化合物的主要代谢物。结果:在乙基硅氧烷/二氧化硅杂交C18柱上达到环丙基戊基苯基和癸酰芬太基的基线分离,保留时间分别为6.79和7.35分钟。由人肝微粒体形成的2种类似物的主要代谢物不同,主要的生物转化是N-丙基戊基戊基和癸酰芬太基的羧化。我们通过明确识别环丙基芬太尼,以及其代谢物,在2个正宗的淘汰后血液样品中证明了2种方法的有用性。结论:在这项研究中,我们成功地证明了环丙基戊基丁基和癸酰芬太基可以通过法医实验室中常用的方法来区分。

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