Egyszerű nézet

dc.contributor.author Kalász Huba
dc.contributor.author Szegi Péter
dc.contributor.author Jánoki G
dc.contributor.author Balogh Lajos
dc.contributor.author Pöstényi Zita
dc.contributor.author Tekes Kornélia
dc.date.accessioned 2014-11-03T09:38:53Z
dc.date.available 2014-11-03T09:38:53Z
dc.date.issued 2013
dc.identifier.citation pagination=2137-2144;journalVolume=20;journalIssueNumber=16;journalTitle=CURRENT MEDICINAL CHEMISTRY; hu
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/376
dc.identifier.uri doi:10.2174/0929867311320160006
dc.description.abstract K203 is an experimental bis-pyridinium mono-aldoxime type cholinesterase reactivator of potential use in organophosphate/ organophosphonate poisoning. Pharmacokinetics of K203 were examined in Wistar rats and beagle dogs using ion-pair HPLC. Serum and cerebrospinal fluid concentrations of K203 were determined using ion-pair reversedphase chromatography on octadecyl silica column. HPLC with ultraviolet detection was used for determination of serum concentration of K203 higher than 0.1 μg/mL while its low concentrations in cerebrospinal fluid required electrochemical detection (0.015 through 4 μg/mL range). In rats the serum levels of K203 followed zero order pharmacokinetics from 15 to 120 minutes post administration. Zero order pharmacokinetics was also observed in beagle dogs after low dose (15 μmol/kg) of K203 administration. High dose administration (250 ?mol/kg) led to subsequent hindered elimination from both cerebrospinal fluid and serum. © 2013 Bentham Science Publishers. hu
dc.relation.ispartof urn:issn:0929-8673
dc.title Study on medicinal chemistry of k203 in wistar rats and beagle dogs hu
dc.type Journal Article hu
dc.date.updated 2014-09-03T07:46:12Z
dc.language.rfc3066 en hu
dc.identifier.mtmt 2329887
dc.identifier.wos 000317662200006
dc.identifier.pubmed 23531217
dc.contributor.department SE/GYTK/Gyógyszerhatástani Intézet
dc.contributor.institution Semmelweis Egyetem


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