Huang Yu, Du Yu, Hua Zhendong, Liu Cuimei, Jia Wei, Di Bin, Su Mengxiang
School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China.
Anti-Drug Technology Laboratory of Jiangsu Provincial Public Security Bureau, Nanjing 210024, China.
Anal Chem. 2025 Aug 12;97(31):16841-16850. doi: 10.1021/acs.analchem.5c01936. Epub 2025 Jul 29.
Nontargeted screening of new psychoactive substances (NPSs) has always been a challenging task, typically involving data acquisition, the extraction of suspicious peaks, and mass spectrometry elucidation in the screening process. The ongoing advancement of instrument acquisition technology and data analysis methods has resulted in an increasing amount of sample data requiring manual elucidation, significantly reducing the efficiency of forensic identification work and leading to issues such as missed detections and false positives. This study proposed a novel nontargeted screening strategy that is capable of automatically elucidating the NPS classes and chemical structures of unknown designer drugs. For practical use, we applied electron-activated dissociation (EAD) technology to analyze 181 synthetic cannabinoids (SCs) and developed novel mass spectrometry intelligent elucidation (MSIE) software to achieve the nontargeted screening of NPSs and automated structural elucidation of SCs. MSIE software comprises an NPS nontargeted screening model, an SC subclass classification model, and a mass spectrometry intelligent elucidation algorithm. The NPS nontargeted screening model was trained on CID data from 505 NPSs, achieving the classification of 8 NPS classes, with the highest F1 score reaching 93.3%. The SC subclass classification model was trained on EAD data from 181 SCs, achieving the classification of 7 SC parent structures, with the highest F1 score reaching 95.3%. The mass spectrometry intelligent elucidation algorithm includes functionalities such as candidate chemical structure generation, spectral prediction, candidate structure scoring, and fragment ion peak matching, all without any manual intervention throughout the entire process.
新型精神活性物质(NPSs)的非靶向筛查一直是一项具有挑战性的任务,在筛查过程中通常涉及数据采集、可疑峰提取以及质谱解析。仪器采集技术和数据分析方法的不断进步导致需要人工解析的样本数据量不断增加,显著降低了法医鉴定工作的效率,并引发漏检和误报等问题。本研究提出了一种新型非靶向筛查策略,能够自动解析未知设计药物的NPS类别和化学结构。为实际应用,我们应用电子激活解离(EAD)技术分析了181种合成大麻素(SCs),并开发了新型质谱智能解析(MSIE)软件,以实现NPSs的非靶向筛查和SCs的结构自动解析。MSIE软件包括一个NPS非靶向筛查模型、一个SCs子类分类模型和一种质谱智能解析算法。NPS非靶向筛查模型基于505种NPSs的CID数据进行训练,实现了8种NPS类别的分类,最高F1分数达到93.3%。SCs子类分类模型基于181种SCs的EAD数据进行训练,实现了7种SCs母体结构的分类,最高F1分数达到95.3%。质谱智能解析算法包括候选化学结构生成、光谱预测、候选结构评分和碎片离子峰匹配等功能,整个过程无需任何人工干预。