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Mass spectrometric differentiation of the isomers of mono-methoxyethylamphetamines and mono-methoxydimethylamphetamines by GC–EI–MS–MS

Authors :
Koichi Suzuki
Yuki Sakamoto
Shuntaro Matsuta
Kento Tsuboi
Takako Sato
Hiroshi Nishioka
Haruhiko Miyagawa
Kei Zaitsu
Michiaki Tatsuno
Hitoshi Tsuchihashi
Akira Ishii
Munehiro Katagi
Source :
Forensic Toxicology. 31:292-300
Publication Year :
2013
Publisher :
Springer Science and Business Media LLC, 2013.

Abstract

Mass spectrometric differentiation of the six isomers of mono-methoxyethylamphetamines (MeO-EAs) and mono-methoxydimethylamphetamines (MeO-DMAs) by gas chromatography–electron ionization–tandem mass spectrometry (GC–EI–MS–MS) was investigated. Based on their EI-mass spectra, the fragment ions at m/z 121 and 72 were selected as precursor ions for their regioisomeric and structurally isomeric differentiation, respectively. Collision-induced dissociation provides intensity differences in product ions among the isomers, enabling mass spectrometric differentiation of the isomers. Furthermore, high reproducibility of the product ion spectra at the optimized collision energy was confirmed, demonstrating the reliability of the method. To our knowledge, this is the first report on mass spectrometric differentiation of the six isomers of MeO-EAs and MeO-DMAs by GC–EI–MS–MS. Isomeric differentiation by GC–EI–MS–MS has a high potential to discriminate isomers of newly encountered designer drugs, making GC–MS–MS a powerful tool in the forensic toxicology field.

Details

ISSN :
18608973 and 18608965
Volume :
31
Database :
OpenAIRE
Journal :
Forensic Toxicology
Accession number :
edsair.doi...........95fa7a55120f94ec230db8275f9fd0f6