Application of a simultaneous screening method for the detection of new psychoactive substances in various matrix samples using liquid chromatography/electrospray ionization tandem mass spectrometry and liquid chromatography/quadrupole time‐of‐flight mass spectrometry

化学 色谱法 检出限 电喷雾电离 质谱法 电喷雾 液相色谱-质谱法 碎片(计算) 串联质谱法 四极飞行时间 基质(化学分析) 分析化学(期刊) 计算机科学 操作系统
作者
Nam Sook Kim,Na Young Lim,Hwan Seong Choi,Ji Hyun Lee,Hyung-Il Kim,Ji Hyun Lee
出处
期刊:Rapid Communications in Mass Spectrometry [Wiley]
卷期号:35 (10) 被引量:4
标识
DOI:10.1002/rcm.9067
摘要

Rationale Recently, new psychoactive substances (NPS) have emerged as a public health risk. Particularly, their chemical structures are modified to avoid detection. Synthetic NPS with effects similar to those of illegal drugs have been recently detected and synthesized worldwide, including MDMB‐FUBINACA and APINAC, making it essential to rapidly and accurately detect NPS. Methods Fourteen NPS with similar structures were selected and their structures identified using 1 H and 13 C NMR spectroscopy. Additionally, we proposed the fragmentation pattern of each compound using liquid chromatography/quadrupole time‐of‐flight mass spectrometry (LC/QTOF‐MS). A simultaneous analytical method using liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI‐MS/MS) was also developed and applied to real samples to detect the 14 NPS. The method was validated based on the specificity, linearity, limit of detection (LOD), limit of quantification (LOQ), precision, accuracy, matrix effect, and stability according to international validation guidelines. Results The established method was used to screen 65 different matrix samples using LC/ESI‐MS/MS. By comparing the calculated product ion ratios with those of standards, 2C‐B in one of the real samples and 5F‐MDMB‐PICA in 20 samples were identified. For re‐confirmation of detected compounds, the fragmentation pattern of each compound was compared with that of each standard using LC/QTOF‐MS. Conclusions In this study, LC/QTOF‐MS data were used to elucidate the structures and fragmentation patterns of 14 NPS. A simultaneous method was developed using LC/ESI‐MS/MS, which was applied to 65 real samples. The presented method and results can assist in ensuring the safety of public health from illegal adulteration.
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