Pregled bibliografske jedinice broj: 634
Phenyl-imidazolium and quinuclidinium oximes as antidotes against organophosphorus and carbamate poisoning
Phenyl-imidazolium and quinuclidinium oximes as antidotes against organophosphorus and carbamate poisoning // The Second Chemical and Biological Medical Tretment Symposium : proceedings / Price, Richard (ur.).
Spiez: ASA, 1997. str. 37-38 (poster, međunarodna recenzija, cjeloviti rad (in extenso), znanstveni)
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Naslov
Phenyl-imidazolium and quinuclidinium oximes as
antidotes against organophosphorus and
carbamate poisoning
(Phenyl-imidazolium and quinuclidinium oximes as
antidotes against organophosporus and carbamate
poisoning)
Autori
Radić, Božica ; Lucić, Ana ; Primožič, Ines ; Rončević, Renata ; Binenfeld, Zlatko
Vrsta, podvrsta i kategorija rada
Radovi u zbornicima skupova, cjeloviti rad (in extenso), znanstveni
Izvornik
The Second Chemical and Biological Medical Tretment Symposium : proceedings
/ Price, Richard - Spiez : ASA, 1997, 37-38
Skup
Chemical and Biological Medical Tretment Symposium
Mjesto i datum
Spiez, Švicarska, 07.07.1996. - 12.07.1996
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
quinuclidinium oxime ; AChE ; dichlorvos ; carbamates ; propoxur ; carbaryl ; soman
Sažetak
The in vitro activity of human erythrocyte acetylcholinesterase (AChE) and protective activity against soman dichlorovos, and propoxur poisoning in male mice (in vivo experiments) were determined by using bis- phenyl imidazolium (2B) and imidazole- quinuclidinium oximes (BM-1). Oxime 2B strongly inhibits the AChE, and has a good reacitvation potency, but weak protective ability, against AChE inhibited by these agents. Oxime BM-1 inhibits weakly AChE and its in vitro activity against inhibited AChE is negligible. In vivo, this oxime is a very good protective agent against inhibitors tested in this paper. BM-1, given with atropine sulphate, provided a 100 % protection in male mice gainsit 4 x LD 50 soman, 11 x LD 50 dichlorovos, and 16 x LD 50 propoxur, respecitvely. The results indicate that in vivo effectiveness of quinuclidinium oxime is not related to its reactivatin or protective potentials for AChe, as shown by the in vitro experiments. The in vivo action of this BM-1 oxime must be attributed to mechanism not yet well defined.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
00220105
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Renata Odžak
(autor)
Zlatko Binenfeld
(autor)
Ana Lucić Vrdoljak
(autor)
Ines Primožič
(autor)
Božica Radić
(autor)