Skip to main content
Top
Published in: International Journal of Legal Medicine 2/2012

01-03-2012 | Original Article

Studies on the phase I metabolism of the new designer drug 3-fluoromethcathinone using rabbit liver slices

Authors: Evelyn Pawlik, Gerd Plässer, Hellmut Mahler, Thomas Daldrup

Published in: International Journal of Legal Medicine | Issue 2/2012

Login to get access

Abstract

The metabolism of the novel designer drug 3-fluoromethcathinone (3-FMC), sold as “legal highs”, was investigated in vitro via cryopreserved rabbit liver slices. The pharmacological properties and toxicological effects of 3-FMC and its metabolites are not known yet. It can be assumed that 3-FMC will cause effects similar to 4-methylmethcathinone (mephedrone) and methcathinone. For the metabolism studies, pretests were performed with rabbit liver slices incubated with kavain to evaluate optimal conditions. Finally, six known metabolites of kavain were revealed and therefore sufficient information about the suitability of the enzyme system of the rabbit liver slices was obtained. Under optimized conditions, 3-FMC was added to Krebs–Henseleit buffer, pH 7.4 containing NADPH and bicarbonate and incubated with a single rabbit liver slice at 37°C. The metabolism was monitored at 5, 30 and 180 min, respectively. The metabolites formed via the former cryopreserved rabbit liver slices were examined by LC/MS-TOF. Metabolites were identified by their exact masses and isotopic patterns. 3-Fluorocathinone, 3-fluorocathinone-imine, hydroxy-3-fluoromethcathinone and 3-fluoromethcathinone-diol were formed as the main metabolites.
Literature
1.
go back to reference Belhadj-Tahar H, Sadeg N (2005) Methcathinone: a new postindustrial drug. Forensic Sci Int 153:99–101PubMedCrossRef Belhadj-Tahar H, Sadeg N (2005) Methcathinone: a new postindustrial drug. Forensic Sci Int 153:99–101PubMedCrossRef
3.
go back to reference Archer PR (2009) Fluoromethcathinone, a new substance of abuse. Forensic Sci Int 185(1–3):10–20PubMedCrossRef Archer PR (2009) Fluoromethcathinone, a new substance of abuse. Forensic Sci Int 185(1–3):10–20PubMedCrossRef
4.
go back to reference Brandt SD, Sumnall HR, Measham F, Cole J (2010) Analyses of second-generation ‘legal highs’in the UK: initial findings. Drug Test Anal 2(8):377–382PubMedCrossRef Brandt SD, Sumnall HR, Measham F, Cole J (2010) Analyses of second-generation ‘legal highs’in the UK: initial findings. Drug Test Anal 2(8):377–382PubMedCrossRef
5.
go back to reference Tarbah AF (2003) Analytical studies on the kavain metabolism in human specimen and liver cell lines. Dissertation, Heinrich-Heine University Tarbah AF (2003) Analytical studies on the kavain metabolism in human specimen and liver cell lines. Dissertation, Heinrich-Heine University
6.
go back to reference Krebs AH, Henseleit K (1932) Untersuchungen über die Harnstoffbildung im Tierkörper. Hoppe-Seyler‘s Zeitschrift f. physiol. Chemie 33–66 Krebs AH, Henseleit K (1932) Untersuchungen über die Harnstoffbildung im Tierkörper. Hoppe-Seyler‘s Zeitschrift f. physiol. Chemie 33–66
7.
go back to reference Deutsch W (1936) An improvement of Warburg’s method for cutting tissue slices for respiratory experiments. Proc Physiol Soc J Physiol 87:56–57 Deutsch W (1936) An improvement of Warburg’s method for cutting tissue slices for respiratory experiments. Proc Physiol Soc J Physiol 87:56–57
8.
go back to reference Härtter S (2000) In vitro Methoden zur Untersuchung des Phase-I Metabolismus. Pharmazie in unserer Zeit 29(6):365–371PubMedCrossRef Härtter S (2000) In vitro Methoden zur Untersuchung des Phase-I Metabolismus. Pharmazie in unserer Zeit 29(6):365–371PubMedCrossRef
9.
go back to reference Panoutsopoulos IG (2005) Phenylacetaldehyde oxidation by freshly prepared and cryopreserved guinea pig liver slices: the role of aldehyde oxidase. Int J Toxicol 24(2):103–109PubMedCrossRef Panoutsopoulos IG (2005) Phenylacetaldehyde oxidation by freshly prepared and cryopreserved guinea pig liver slices: the role of aldehyde oxidase. Int J Toxicol 24(2):103–109PubMedCrossRef
10.
go back to reference Lisboa PB, Knuppen R, Breuer H (1965) Stoffwechsel von 7-substituierten phenolischen Steroiden in der Rattenleber. Biochim Biophys Acta 97(3):557–563PubMedCrossRef Lisboa PB, Knuppen R, Breuer H (1965) Stoffwechsel von 7-substituierten phenolischen Steroiden in der Rattenleber. Biochim Biophys Acta 97(3):557–563PubMedCrossRef
11.
go back to reference Markantonis LS, Kyroudis A, Beckett HA (1986) The stereoselective metabolism of dimethylpropion and monomethylpropion. Biochem Pharmacol 35(3):529–532PubMedCrossRef Markantonis LS, Kyroudis A, Beckett HA (1986) The stereoselective metabolism of dimethylpropion and monomethylpropion. Biochem Pharmacol 35(3):529–532PubMedCrossRef
12.
go back to reference Brenneisen R, Geisshüsler S, Schorno X (1986) Metabolism of cathinone to (-)-norephedrine and (-)-norpseudoephedrine. J Pharm Pharmacol 38(4):298–300PubMedCrossRef Brenneisen R, Geisshüsler S, Schorno X (1986) Metabolism of cathinone to (-)-norephedrine and (-)-norpseudoephedrine. J Pharm Pharmacol 38(4):298–300PubMedCrossRef
13.
go back to reference Kraemer T, Maurer HH (2002) Toxicokinetics of amphetamines: metabolism and toxicokinetic data of designer drugs, amphetamine, methamphetamine, and their N-alkyl derivates. Therapeutic Drug Monitoring 24:277–289PubMedCrossRef Kraemer T, Maurer HH (2002) Toxicokinetics of amphetamines: metabolism and toxicokinetic data of designer drugs, amphetamine, methamphetamine, and their N-alkyl derivates. Therapeutic Drug Monitoring 24:277–289PubMedCrossRef
14.
go back to reference Wright J, Cho AK, Gal J (1977) The metabolism of amphetamine in vitro by rabbit liver preparations: a comparison of R(-) and S (+) enantiomers. Xenobiotica 7(5):257–266PubMedCrossRef Wright J, Cho AK, Gal J (1977) The metabolism of amphetamine in vitro by rabbit liver preparations: a comparison of R(-) and S (+) enantiomers. Xenobiotica 7(5):257–266PubMedCrossRef
15.
go back to reference Meyer RM, Maurer HH (2010) Metabolism and toxicological detection of emerging drugs of abuse in Germany and Israel (2010) at annual meeting abstract: abstracts from the join American-Israeli Medical Toxicology and the Israel Society of Toxicology November 16–17, Rambam, Medical Center, Haifa, Israel. J Med Toxicol Meyer RM, Maurer HH (2010) Metabolism and toxicological detection of emerging drugs of abuse in Germany and Israel (2010) at annual meeting abstract: abstracts from the join American-Israeli Medical Toxicology and the Israel Society of Toxicology November 16–17, Rambam, Medical Center, Haifa, Israel. J Med Toxicol
16.
go back to reference Meyer RM, Wilhelm J, Peters TF, Maurer HH (2010) Beta-keto amphetamines: studies on the metabolism of the designer drugs mephedrone and toxicological detection of mephedrone, butylone, and methylone in urine using gas chromatography-mass spectrometry. Anal Bioanal Chem 397(3):1225–1233PubMedCrossRef Meyer RM, Wilhelm J, Peters TF, Maurer HH (2010) Beta-keto amphetamines: studies on the metabolism of the designer drugs mephedrone and toxicological detection of mephedrone, butylone, and methylone in urine using gas chromatography-mass spectrometry. Anal Bioanal Chem 397(3):1225–1233PubMedCrossRef
Metadata
Title
Studies on the phase I metabolism of the new designer drug 3-fluoromethcathinone using rabbit liver slices
Authors
Evelyn Pawlik
Gerd Plässer
Hellmut Mahler
Thomas Daldrup
Publication date
01-03-2012
Publisher
Springer-Verlag
Published in
International Journal of Legal Medicine / Issue 2/2012
Print ISSN: 0937-9827
Electronic ISSN: 1437-1596
DOI
https://doi.org/10.1007/s00414-011-0601-6

Other articles of this Issue 2/2012

International Journal of Legal Medicine 2/2012 Go to the issue