Kei Zaitsu, Munehiro Katagi, Tooru Kamata, Hiroe Kamata, Noriaki Shima, Hitoshi Tsuchihashi, Takeshi Hayashi, Hisanaga Kuroki, Ryoji Matoba
Index: Forensic Sci. Int. 177(1) , 77-84, (2008)
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A newly synthesized designer drug, para-methoxyethylamphetamine (PMEA) was unexpectedly detected in the postmortem specimens of fatality involving drug intoxication in 2005, Japan. For unequivocal identification, the isomeric discrimination of PMEA and its positional-isomers was performed by GC/MS with the trifluoroacetylation. In order to prove the intake of PMEA, the characteristic metabolites of PMEA were also identified by GC/MS analysis of the urine specimen with trifluoroacetylation. As a result, para-methoxyamphetamine, para-hydroxyethylamphetamine (POHEA) and para-hydroxyamphetamine were identified as the major metabolites of PMEA. For the quantitative analyses of PMEA and its three metabolites in body fluids, an automated column-switching LC/MS procedure was developed, and applied to the postmortem blood and urine specimens. In this fatal case, blood concentration of PMEA was estimated to be 12.2 microg/mL and this level seemed extremely high in comparison with lethal blood-levels of its analogues, representing acute-intoxication of the victim. Based on the quantitative results, PMEA was found to be extensively metabolized to POHEA via O-demethylation, partly followed by its conjugation.
Structure | Name/CAS No. | Molecular Formula | Articles |
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4-Methoxy Methamphetamine Hydrochloride
CAS:3398-68-3 |
C11H18ClNO |
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1988-09-01 [Pharmacol. Biochem. Behav. 31(1) , 9-13, (1988)] |
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