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实时直接分析质谱与碰撞诱导解离在合成大麻素结构分析中的应用。

Direct analysis in real time mass spectrometry with collision-induced dissociation for structural analysis of synthetic cannabinoids.

机构信息

Department of Chemistry, University at Albany, State University of New York (SUNY), 1400 Washington Ave., Albany, NY 12222, USA.

出版信息

Rapid Commun Mass Spectrom. 2012 Oct 15;26(19):2335-42. doi: 10.1002/rcm.6354.

Abstract

RATIONALE

The emergence of numerous cannabinoid designer drugs has been tied to large spikes in emergency room visits and overdoses. Identifying these substances is difficult for the following reasons: (1) the compounds are novel, closely structurally related, and do not usually test positive in drug screens; (2) novel analogs rapidly appear on the market; (3) no standard protocols exist for their identification; and (4) customized and extensive sample preparation/extraction and analysis procedures are required to demonstrate their presence.

METHODS

Direct analysis in real time mass spectrometry (DART-MS) employing collision-induced dissociation (CID) provided confirmatory structural information that was useful in characterizing the various cannabinoid analogs, including those contained in mixtures. CID analysis illustrated that, although closely related compounds fragment in a similar fashion, their structural differences still resulted in multiple diagnostic peaks that provided additional confidence towards structural identification.

RESULTS

DART-MS spectra were acquired under CID conditions to rapidly differentiate among five synthetic cannabinoids contained within 'herbal' products purchased locally in New York State (USA). The spectra exhibited M+H ions and product ions unique to each cannabinoid that corresponded to major structural features. Five different cannabinoid analogs, alone and as mixtures of at least two cannabinoids, were identified in six herbal products and differentiated by their CID product ion patterns.

CONCLUSIONS

Illicit synthetic cannabinoid products continue to be readily available despite national and international restrictions. These products contain a wide range of active components, and, in many cases, multiple active ingredients. DART-MS allows rapid analyses of these synthetic cannabinoids based on the exact masses of their M+H ions and product ion peaks generated using CID.

摘要

理由

许多大麻素设计药物的出现与急诊室就诊和过量用药的大幅增加有关。由于以下原因,识别这些物质具有挑战性:(1) 这些化合物是新颖的,结构上密切相关,通常不会在药物筛选中呈阳性;(2) 新的类似物迅速出现在市场上;(3) 不存在用于鉴定它们的标准协议;(4) 需要定制和广泛的样品制备/提取和分析程序来证明它们的存在。

方法

直接实时分析质谱法 (DART-MS) 采用碰撞诱导解离 (CID) 提供了有用的确认结构信息,有助于对各种大麻素类似物进行特征描述,包括混合物中的类似物。CID 分析表明,尽管密切相关的化合物以相似的方式碎裂,但它们的结构差异仍然导致多个诊断峰,从而为结构鉴定提供了额外的信心。

结果

在 CID 条件下采集 DART-MS 光谱,以快速区分在纽约州(美国)当地购买的“草药”产品中包含的五种合成大麻素。这些光谱显示出 M+H 离子和每种大麻素特有的产物离子,这些离子对应于主要结构特征。在六种草药产品中鉴定出五种不同的大麻素类似物,单独存在或作为至少两种大麻素的混合物存在,并通过其 CID 产物离子模式进行区分。

结论

尽管受到国家和国际限制,非法合成大麻素产品仍在大量供应。这些产品包含广泛的活性成分,在许多情况下,包含多种活性成分。DART-MS 允许根据 M+H 离子的精确质量以及使用 CID 生成的产物离子峰对这些合成大麻素进行快速分析。

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