Kratko priopćenje
https://doi.org/10.2478/10004-1254-61-2010-1985
Qualitative GC-MS Assessment of TCP and TAMORF Elimination in Rats
Maja Jelena Petek
orcid.org/0000-0002-3659-1725
; Forensic Science Centre “Ivan Vučetić”, Zagreb, Croatia
Ana Lucić Vrdoljak
; Institute for Medical Research and Occupational Health, Zagreb, Croatia
Gordan Mršić
; Forensic Science Centre “Ivan Vučetić”, Zagreb, Croatia
Sažetak
Nerve agents are highly toxic organophosphorus (OP) compounds. They inhibit acetylcholinesterase (AChE), an enzyme that hydrolyses acetycholine (ACh) in the nervous system. Pathophysiological changes caused by OP poisonings are primarily the consequence of surplus ACh on cholinergic receptors and in the central nervous system. Standard treatment of OP poisoning includes combined administration of carbamates, atropine, oximes and anticonvulsants. In order to improve therapy, new compounds have been synthesised and tested. Tenocyclidine (TCP) and its adamantane derivative 1-[2-(2-thienyl)-2-adamantyl] morpholine (TAMORF) have shown interesting properties against soman poisoning. In this study, we
developed a qualitative GC-MS method to measure elimination of TCP and TAMORF through rat urine in order to learn more about the mechanisms through which TCP protects an organism from OP poisoning and to determine the duration of this protective effect. GC-MS showed that six hours after treatment with TCP, rat urine contained only its metabolite 1-thienylcyclohexene, while urine of rats treated with TAMORF contained both TAMORF and its metabolites.
Ključne riječi
antidote; metabolite; qualitative method; urine; tenocyclidine
Hrčak ID:
49020
URI
Datum izdavanja:
17.3.2010.
Posjeta: 1.636 *