Please use this identifier to cite or link to this item: doi:10.22028/D291-43624
Title: Are the postmortem concentration changes of the synthetic cannabinoid cumyl-5F-P7AICA and its N-pentanoic acid metabolite dependent on the environmental conditions? - A systematic study following pulmonary administration to pigs
Author(s): Walle, Nadja
Doerr, Adrian A.
Peters, Benjamin
Laschke, Matthias W.
Menger, Michael D.
Schmidt, Peter H.
Meyer, Markus R.
Schaefer, Nadine
Language: English
Title: Toxicology Letters
Volume: 401
Pages: 170-180
Publisher/Platform: Elsevier
Year of Publication: 2024
Free key words: Synthetic cannabinoids
cumyl-5F-P7AICA
7-azaindole
Pigs
Postmortem redistribution
DDC notations: 610 Medicine and health
Publikation type: Journal Article
Abstract: The number of fatal cases involving synthetic cannabinoids (SCs) is increasing. However, interpretation of postmortem (PM) toxicological findings is challenging, due to unknown PM intervals and possible redistribution processes or instabilities. Only sparse data on SCs are available. Therefore, a controlled pig study was performed to determine the PM stability of cumyl-5F-P7AICA under different environmental conditions. Ten pigs inhalatively received 200 µg/kg body weight cumyl-5F-P7AICA each. Six hours later, they were euthanized and biopsies of the main tissues and body fluids were taken. Animals were stored in air or water (n=5 each) and samples were repeatedly taken for three days. Quantification of cumyl-5F-P7AICA and its N-pentanoic acid metabolite (NPA) was performed using standard addition or a fully validated method (blood) followed by LC-MS/MS. Timedependent concentration changes of cumyl-5F-P7AICA were observed in liver, bile fluid and muscle specimens at both conditions. Concentrations of NPA only changed considerably in duodenum content of animals stored in air. Environment-dependent concentrations changes were only observed for cumyl-5F-P7AICA in kidney and the NPA metabolite in duodenum content. Overall, cumyl-5F-P7AICA and its metabolite seem to be quite stable in PM specimens. Hence, also central blood might be analyzed, if no peripheral blood is available.
DOI of the first publication: 10.1016/j.toxlet.2024.10.006
URL of the first publication: https://doi.org/10.1016/j.toxlet.2024.10.006
Link to this record: urn:nbn:de:bsz:291--ds-436248
hdl:20.500.11880/39082
http://dx.doi.org/10.22028/D291-43624
ISSN: 1879-3169
Date of registration: 2-Dec-2024
Description of the related object: Supporting information
Related object: https://ars.els-cdn.com/content/image/1-s2.0-S037842742402040X-mmc1.docx
Faculty: M - Medizinische Fakultät
Department: M - Chirurgie
M - Experimentelle und Klinische Pharmakologie und Toxikologie
M - Rechtsmedizin
Professorship: M - Prof. Dr. Michael D. Menger
M - Prof. Dr. Markus Meyer
M - Keiner Professur zugeordnet
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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