Metabolism and toxicological detection of the designer drug 4-iodo-2,5-dimethoxy-amphetamine (DOI) in rat urine using gas chromatography-mass spectrometry
- PMID: 17632045
- DOI: 10.1016/j.jchromb.2007.06.027
Metabolism and toxicological detection of the designer drug 4-iodo-2,5-dimethoxy-amphetamine (DOI) in rat urine using gas chromatography-mass spectrometry
Abstract
The amphetamine-derived designer drug 4-iodo-2,5-dimethoxy-amphetamine (DOI) is an upcoming substance on the illicit drug market. In the current study, the identification of its metabolites in rat urine and their toxicological detection in the authors' systematic toxicological analysis (STA) procedure were examined. DOI is extensively metabolized by O-demethylation and beside small amounts of parent compound it was found to be excreted mainly in form of metabolites. The STA procedure using full-scan GC-MS allowed proving an intake of a common drug users' dose of DOI by detection of the two O-demethyl metabolite isomers in rat urine. Assuming similar metabolism, the described STA procedure should be suitable for proof of an intake of DOI in human urine.
Similar articles
-
Designer drugs 2,5-dimethoxy-4-bromo-amphetamine (DOB) and 2,5-dimethoxy-4-bromo-methamphetamine (MDOB): studies on their metabolism and toxicological detection in rat urine using gas chromatographic/mass spectrometric techniques.J Mass Spectrom. 2006 Apr;41(4):487-98. doi: 10.1002/jms.1007. J Mass Spectrom. 2006. PMID: 16470568
-
Studies on the toxicological detection of the designer drug 4-bromo-2,5-dimethoxy-beta-phenethylamine (2C-B) in rat urine using gas chromatography-mass spectrometry.J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Feb 1;846(1-2):374-7. doi: 10.1016/j.jchromb.2006.08.049. Epub 2006 Sep 15. J Chromatogr B Analyt Technol Biomed Life Sci. 2007. PMID: 16978931
-
Designer drug 2,5-dimethoxy-4-methyl-amphetamine (DOM, STP): involvement of the cytochrome P450 isoenzymes in formation of its main metabolite and detection of the latter in rat urine as proof of a drug intake using gas chromatography-mass spectrometry.J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Feb 1;862(1-2):252-6. doi: 10.1016/j.jchromb.2007.11.042. Epub 2007 Dec 8. J Chromatogr B Analyt Technol Biomed Life Sci. 2008. PMID: 18155651
-
The role of gas chromatography/mass spectrometry. Instrumental techniques in forensic urine drug testing.Clin Lab Med. 1998 Dec;18(4):631-49. Clin Lab Med. 1998. PMID: 9891603 Review.
-
Trends in bioanalytical methods for the determination and quantification of club drugs: 2000-2010.Biomed Chromatogr. 2011 Jan;25(1-2):300-21. doi: 10.1002/bmc.1549. Epub 2010 Nov 8. Biomed Chromatogr. 2011. PMID: 21061455 Review.
Cited by
-
Microwave-assisted derivatization procedures for gas chromatography/mass spectrometry analysis.Mol Divers. 2010 Nov;14(4):869-88. doi: 10.1007/s11030-010-9242-9. Epub 2010 Mar 12. Mol Divers. 2010. PMID: 20225067 Review.
-
Radiosynthesis and in vivo evaluation of a series of substituted 11C-phenethylamines as 5-HT (2A) agonist PET tracers.Eur J Nucl Med Mol Imaging. 2011 Apr;38(4):681-93. doi: 10.1007/s00259-010-1686-8. Epub 2010 Dec 21. Eur J Nucl Med Mol Imaging. 2011. PMID: 21174090
-
Comparison of the behavioral responses induced by phenylalkylamine hallucinogens and their tetrahydrobenzodifuran ("FLY") and benzodifuran ("DragonFLY") analogs.Neuropharmacology. 2019 Jan;144:368-376. doi: 10.1016/j.neuropharm.2018.10.037. Epub 2018 Oct 29. Neuropharmacology. 2019. PMID: 30385253 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous