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在系统降解前后对盐酸芬太尼粉末进行表征。

Characterization of fentanyl HCl powder prior to and after systematic degradation.

机构信息

School of Forensic Sciences, Oklahoma State University Center for Health Sciences, Tulsa, Oklahoma, USA.

出版信息

J Forensic Sci. 2022 Sep;67(5):1979-1988. doi: 10.1111/1556-4029.15074. Epub 2022 Jun 7.

DOI:10.1111/1556-4029.15074
PMID:35670248
Abstract

Fentanyl HCl is of particular interest in forensic cases but there is a notable gap in literature regarding its analysis. This study utilized a multi-method approach to characterize fentanyl HCl powder, both fresh and following a forced degradation process. Using sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) and direct injection gas chromatography-mass spectrometry (GC-MS), five compounds were identified in fresh fentanyl HCl powder. The identified compounds were: N-phenylpropanamide, 1-phenethyl-4-propionyloxypiperidine (1-P-4-POP), 4-anilino-N-phenethylpiperidine (4-ANPP), acetylfentanyl, and fentanyl; all identified compounds but acetylfentanyl and fentanyl decreased in quantity as the sample was degraded. Fresh headspace samples analyzed with solid phase microextraction (SPME)-GC-MS identified four compounds in common with the powder analyses: N-phenylpropanamide,1-P-4-POP, 4-ANPP, and fentanyl. Acetylfentanyl was not present in the headspace samples, although two additional compounds were: N-phenylacetamide and N-phenethyl-4-piperidinone (NPP). Where direct analysis of degraded fentanyl HCl showed decreased quantities of the identified compounds, headspace samples of the degraded fentanyl HCl resulted in higher quantities, implying that the degradation process drove those compounds to volatilize. Notably, fentanyl was identified in the headspace, implying that this could be an appropriate target for standoff detection. Finally, thermogravimetric analysis (TGA) and differential scanning calorimetry (DCS) confirmed that the forced degradation process had little permanent effect on the powder.

摘要

盐酸芬太尼在法医案件中特别受关注,但关于其分析的文献却存在明显的空白。本研究采用多方法手段对新鲜和强制降解后的盐酸芬太尼粉末进行了特征描述。使用灵敏的液相色谱-串联质谱(LC-MS/MS)和直接进样气相色谱-质谱(GC-MS),在新鲜的盐酸芬太尼粉末中鉴定出了五种化合物。鉴定出的化合物为:N-苯丙酰胺、1-苯乙基-4-丙酰氧基哌啶(1-P-4-POP)、4-苯胺基-N-苯乙基哌啶(4-ANPP)、乙酰芬太尼和芬太尼;所有鉴定出的化合物(除乙酰芬太尼和芬太尼外)的含量随着样品降解而减少。用固相微萃取(SPME)-GC-MS 分析新鲜的顶空样品,与粉末分析鉴定出了四种共同的化合物:N-苯丙酰胺、1-P-4-POP、4-ANPP 和芬太尼。在顶空样品中没有发现乙酰芬太尼,但有两种额外的化合物:N-苯乙酰胺和 N-苯乙基-4-哌啶酮(NPP)。在直接分析降解的盐酸芬太尼时,发现鉴定出的化合物数量减少,而降解的盐酸芬太尼的顶空样品则导致数量增加,这表明降解过程促使这些化合物挥发。值得注意的是,在顶空样品中鉴定出了芬太尼,这表明这可能是一种合适的远距离检测目标。最后,热重分析(TGA)和差示扫描量热法(DCS)证实,强制降解过程对粉末的永久影响很小。

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