Abstract

The still increasing number of drugs of abuse, particularly the so-called new psychoactive substances (NPS), poses an analytical challenge for clinical and forensic toxicologists but also for doping control. NPS usually belong to various classes such as synthetic cannabinoids, phenethylamines, opioids, or benzodiazepines. Like other xenobiotics, NPS undergo absorption, distribution, metabolism, and excretion processes after consumption, but only very limited data concerning their toxicokinetics and safety properties is available once they appear on the market. The inclusion of metabolites in mass spectral libraries is often crucial for the detection of NPS especially in urine screening approaches. Authentic human samples may represent the gold standard for identification of metabolites but are often not available and clinical studies cannot be performed due to ethical concerns. However, numerous alternative in vitro and in vivo models are available. This trends article will give an overview on selected models, discuss current studies, and highlight recent developments.

Highlights

  • Development and application of analytical screening procedures to identify xenobiotics in human biosamples are amongst the main tasks in clinical and forensic toxicology and in related fields such as doping control

  • Traditional in vitro and in vivo tools to study the metabolism of new psychoactive substances (NPS)

  • Well-established in vitro systems to study the metabolism of NPS for identification of human biomarkers are human liver microsomes (HLM) and the human liver S9 fraction (HLS9) [2,3,4]

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Summary

Introduction

Development and application of analytical screening procedures to identify xenobiotics in human biosamples are amongst the main tasks in clinical and forensic toxicology and in related fields such as doping control. Analytical data of the screened compounds need to be known. This includes their mass spectra and retention times in a certain setting. To collect this information of parent compounds is often not very challenging as most compounds can be purchased in case of therapeutic drugs or are available from. Published in the topical collection Recent Trends in (Bio)Analytical Chemistry with guest editors Antje J.

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