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Trace level determination of Δ9‐tetrahydrocannabinol in a perfume using liquid chromatography high resolution tandem mass spectrometry and gas chromatography mass spectrometry
Author(s) -
Thalhamer Bernhard,
Himmelsbach Markus,
Buchberger Wolfgang
Publication year - 2017
Publication title -
flavour and fragrance journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.393
H-Index - 70
eISSN - 1099-1026
pISSN - 0882-5734
DOI - 10.1002/ffj.3344
Subject(s) - chemistry , chromatography , mass spectrometry , high performance liquid chromatography , tandem mass spectrometry , orbitrap , gas chromatography , electrospray ionization , selected reaction monitoring , fragmentation (computing) , analytical chemistry (journal) , computer science , operating system
Δ9‐tetrahydrocannabinol (Δ9‐THC), which is the primary psychoactive ingredient in marijuana, was identified at trace levels in a perfume whose name/brand and its scent aim to arouse associations with marijuana/hashish. The presence of Δ9‐THC was unambiguously confirmed by high performance liquid chromatography (HPLC) coupled with Orbitrap high resolution mass spectrometric detection. The relevant HPLC peak of the analysed perfume shows identical chromatographic behaviour and mass spectrometric fragmentation compared to an authentic reference material of Δ9‐THC. Electrospray ionization was performed in the positive mode, fragmentation was carried out by both collision‐induced dissociation and higher‐energy collisional dissociation. The quantitation of Δ9‐THC in the complex perfume matrix was performed by HPLC combined with a triple quadrupole mass spectrometer (HPLC‐MS/MS) in the multiple reaction monitoring mode. Calibration by the standard addition method yielded a concentration of 0.2 µg Δ9‐THC per ml perfume. Additionally gas chromatography mass spectrometry was also used to confirm the results for Δ9‐THC. It is based on a fundamentally different separation principle and results were in good agreement with HPLC‐MS/MS, which proved the reliability of the analysis. Copyright © 2016 John Wiley & Sons, Ltd.