Department of Chemistry, Western Illinois University, Macomb, IL, 61455, USA.
Mund-Lagowski Department of Chemistry & Biochemistry, Bradley University, Peoria, IL, 61625, USA.
Rapid Commun Mass Spectrom. 2020 Jan 15;34(1):e8558. doi: 10.1002/rcm.8558.
Over the last ten years, helium direct analysis in real time time-of-flight mass spectrometry (He DART-TOFMS) has become an established technique in rapid screening of forensic drugs to decrease the time necessary to triage forensic drug cases, therefore contributing to backlog reduction and more timely criminal prosecution. Recently, we demonstrated that N DART was able to efficiently ionize all polar compounds except for a few extremely small ones such as methanol and acetonitrile. Therefore, N DART-TOFMS should be a suitable technique for rapid screening of forensic drugs.
Nitrogen direct analysis in real time time-of-flight mass spectrometry (N DART-TOFMS) was performed using a JEOL AccuTOF mass spectrometer with an IonSense DART-100 ion source. A 3-min analytical protocol was used for the analysis of each sample. Sample introduction was accomplished by moving the closed end of a melting point capillary where approximately 1 μL sample solution was deposited or the exposed inside of a freshly cut tablet across the N gas stream between the DART-100 ion source and orifice 1 of the AccuTOF.
Ten commonly abused drugs, eight synthetic cannabinoids and four controlled prescription drugs (CPDs) were analyzed. The limit of detection (LOD) was determined to be approximately 10 μg/mL or 10 pg in quantities. All drugs at the LOD level were positively identified using their [M + H] ions with mass errors less than 5 mDa. The identification were further supported by in-source fragment ions and characteristic N DART ions that are not commonly generated by He DART, e.g. [M + H + O] and [M + H + 2O] ions.
It was concluded that the 3-min analytical protocol could be utilized in the analysis of seized drugs in the form of tablets and powders or prepared in solution. In consideration that N is readily available in the air and He is a non-renewable resource, N DART-TOFMS is a greener, cheaper and more convenient alternative to He DART-TOFMS in rapid screening of forensic drugs.
在过去的十年中,氦气实时飞行时间质谱直接分析(He DART-TOFMS)已成为快速筛选法医药物的既定技术,可缩短法医药物案件的分类时间,从而有助于减少积压并更及时地进行刑事起诉。最近,我们证明 N DART 能够有效地使所有极性化合物离子化,除了极少数非常小的化合物,如甲醇和乙腈。因此,N DART-TOFMS 应该是一种快速筛选法医药物的合适技术。
使用配备 IonSense DART-100 离子源的 JEOL AccuTOF 质谱仪进行氮气实时飞行时间质谱直接分析(N DART-TOFMS)。使用 3 分钟的分析方案对每个样品进行分析。通过将熔化点毛细管的封闭端移动到约 1μL 样品溶液沉积的位置或刚刚切割的片剂的暴露内部,将样品引入到氮气流中,该氮气流在 DART-100 离子源和 AccuTOF 的孔 1 之间。
分析了十种常见的滥用药物、八种合成大麻素和四种受控处方药物(CPD)。LOD 确定为约 10μg/mL 或 10pg 量。所有在 LOD 水平的药物都通过其 [M+H]+离子进行了阳性鉴定,其质量误差小于 5 mDa。通过在源内碎片离子和特征 N DART 离子进一步支持鉴定,这些离子通常不由 He DART 产生,例如 [M+H+O] 和 [M+H+2O] 离子。
得出的结论是,3 分钟的分析方案可用于以片剂和粉末形式或在溶液中制备的缴获药物的分析。考虑到 N 在空气中很容易获得,而 He 是一种不可再生资源,因此 N DART-TOFMS 是一种比 He DART-TOFMS 更环保、更便宜且更方便的法医药物快速筛选替代方法。