The metabolic fate of two new psychoactive substances − 2‐aminoindane and N‐methyl‐2‐aminoindane − studied in vitro and in vivo to support drug testing

• Published in: Drug testing and analysis 2020-01, Vol.12 (1), p.145-151
• Main Authors: Manier, Sascha K., Felske, Christina, Eckstein, Niels, Meyer, Markus R.
• Format: Article
• Language: English
• Subjects: aminoindanes; Drug testing; in vitro; in vivo; LC−HRMS/MS; Metabolites; NPS; Psychotropic drugs; Urine
• ISSN: 1942-7603; 1942-7611
• DOI: 10.1002/dta.2699

The aim of this study was to characterize the in vitro and in vivo metabolism of 2‐aminoindane (2,3‐dihydro‐1H‐inden‐2‐amine, 2‐AI), and N‐methyl‐2‐aminoindane (N‐methyl‐2,3‐dihydro‐1H‐inden‐2‐amine, NM‐2‐AI) after incubations using pooled human liver microsomes (pHLMs), pooled human liver S9 fraction (pS9), and rat urine after oral administration. After analysis using liquid chromatography coupled to high‐resolution mass spectrometry, pHLM incubations revealed that 2‐AI was left unmetabolized, while NM‐2‐AI formed a hydroxylamine and diastereomers of a metabolite formed after hydroxylation in beta position. Incubations using pS9 led to the formation of an acetyl conjugation in the case of 2‐AI and merely a hydroxylamine for NM‐2‐AI. Investigations on rat urine showed that 2‐AI was hydroxylated also forming diasteromers as described for NM‐2‐AI or acetylated similar to incubations using pS9. All hydroxylated metabolites of NM‐2‐AI except the hydroxylamine were found in rat urine as additional sulfates. Assuming similar patterns in humans, urine screening procedures might be focused on the parent compounds but should also include their metabolites. An activity screening using human recombinant N‐acetyl transferase (NAT) isoforms 1 and 2 revealed that 2‐AI was acetylated exclusively by NAT2, which is polymorphically expressed. 2‐AI and NM‐2‐AI are two new psychoactive substances. Their metabolisms were investigated using in vitro and in vivo models as well as recombinant enzymes. Both were sparsely metabolized with single hydroxylation, acetylation and sulfation being the only observed metabolic steps.