Please use this identifier to cite or link to this item: doi:10.22028/D291-46204
Title: Studies on the Stability and Microbial Biotransformation of Five Deschloroketamine Derivatives as Prerequisite for Wastewater-Based Epidemiology Screening
Author(s): Frankenfeld, Fabian
Wagmann, Lea
Meyer, Markus R.
Language: English
Title: Drug Testing and Analysis
Volume: 17 (2025)
Issue: 8
Pages: 1336-1343
Publisher/Platform: Wiley
Year of Publication: 2024
Free key words: deschloroketamines
LC-HRMS/MS
microbial biotransformation
new psychoactive substances
wastewater
DDC notations: 610 Medicine and health
Publikation type: Journal Article
Abstract: Wastewater (WW)-based epidemiology (WBE) is a powerful tool for screening and surveillance of drugs (of abuse) or new psy choactive substances (NPSs) in larger population. Since the drug market changes frequently, it is crucial for WBE to define screening and surveillance biomarkers considering drug metabolism and (microbial) stability. The aims of the presented work were first to identify metabolites, potentially serving as a WBE biomarker of five deschloroketamine derivatives (DCKDs) in rat feces samples after oral administration in addition to already known urinary metabolites, and second to elucidate the microbial biotransformation and WW stability of five DCKDs and their metabolites detected in urine and feces. Microbial biotransforma tion and stability of DCKD and their metabolites in WW were assessed by incubating parent compounds at 0.1mg/L or rat urine or rat feces samples in freshly collected, untreated, influent WW over a period of 24h. All samples were analyzed using liquid chromatography–high-resolution tandem mass spectrometry. All parent compounds, seven Phase I, and one Phase II metabolite were detected in rat feces samples. After WW incubations, all tested DCKD and their metabolites were still detectable at least in trace amounts, but particularly, peak areas of the Phase II N- and O-glucuronides showed a markable decrease. This is in line with previous findings where Phase II conjugates were identified to be unstable in WW and thus not recommended as a WW biomarker. Hence, incubations demonstrated that the five DCKD and most of their metabolites were sufficiently stable in WW influent and can thus be used as analytical targets in the context of WBE.
DOI of the first publication: 10.1002/dta.3839
URL of the first publication: https://doi.org/10.1002/dta.3839
Link to this record: urn:nbn:de:bsz:291--ds-462049
hdl:20.500.11880/40499
http://dx.doi.org/10.22028/D291-46204
ISSN: 1942-7611
1942-7603
Date of registration: 8-Sep-2025
Description of the related object: Supporting Information
Related object: https://analyticalsciencejournals.onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fdta.3839&file=dta3839-sup-0001-ESM_revised.docx
Faculty: M - Medizinische Fakultät
Department: M - Experimentelle und Klinische Pharmakologie und Toxikologie
Professorship: M - Prof. Dr. Markus Meyer
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes



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