Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:16302289rdf:typepubmed:Citationlld:pubmed
pubmed-article:16302289lifeskim:mentionsumls-concept:C0034693lld:lifeskim
pubmed-article:16302289lifeskim:mentionsumls-concept:C0031327lld:lifeskim
pubmed-article:16302289lifeskim:mentionsumls-concept:C0022660lld:lifeskim
pubmed-article:16302289lifeskim:mentionsumls-concept:C1280500lld:lifeskim
pubmed-article:16302289lifeskim:mentionsumls-concept:C1433601lld:lifeskim
pubmed-article:16302289pubmed:issue1lld:pubmed
pubmed-article:16302289pubmed:dateCreated2005-12-27lld:pubmed
pubmed-article:16302289pubmed:abstractTextThe pharmacokinetic parameters of DA-7867 were compared after intravenous and oral administration at a dose of 10 mg/kg to control rats and rats with acute renal failure induced by uranyl nitrate (rats with U-ARF). After intravenous administration in rats with U-ARF, the time-averaged total body clearance (Cl) was significantly faster (2.45 versus 0.932 ml/min/kg) than controls due to significantly faster nonrenal clearance (2.25 versus 0.855 ml/min/kg) in rats with U-ARF. The faster nonrenal clearance could be due to significantly greater gastrointestinal (including biliary) excretion; the amount of unchanged DA-7867 recovered from the entire gastrointestinal tract at 24 h was significantly greater (30.3% versus 9.38% of intravenous dose) in rats with U-ARF. In rats with U-ARF, the Vss was significantly larger (1420 ml/kg compared with 580 ml/kg), but this was not due to a difference in plasma protein binding; the values were comparable between the two groups of rats. After oral administration to rats with U-ARF, the total area under the plasma concentration-time from time zero to time infinity (AUC) of DA-7867 was significantly smaller than the controls (2560 microg min/ml versus 7440 microg min/ml), and this was not due mainly to a decrease in absorption from the gastrointestinal tract in rats with U-ARF.lld:pubmed
pubmed-article:16302289pubmed:languageenglld:pubmed
pubmed-article:16302289pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16302289pubmed:citationSubsetIMlld:pubmed
pubmed-article:16302289pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16302289pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16302289pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16302289pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16302289pubmed:statusMEDLINElld:pubmed
pubmed-article:16302289pubmed:monthJanlld:pubmed
pubmed-article:16302289pubmed:issn0142-2782lld:pubmed
pubmed-article:16302289pubmed:authorpubmed-author:KimWon BWBlld:pubmed
pubmed-article:16302289pubmed:authorpubmed-author:LeeInchulIlld:pubmed
pubmed-article:16302289pubmed:authorpubmed-author:LeeMyung GMGlld:pubmed
pubmed-article:16302289pubmed:authorpubmed-author:KwonJong WJWlld:pubmed
pubmed-article:16302289pubmed:authorpubmed-author:BaeSoo KSKlld:pubmed
pubmed-article:16302289pubmed:copyrightInfoCopyright (c) 2005 John Wiley & Sons, Ltd.lld:pubmed
pubmed-article:16302289pubmed:issnTypePrintlld:pubmed
pubmed-article:16302289pubmed:volume27lld:pubmed
pubmed-article:16302289pubmed:ownerNLMlld:pubmed
pubmed-article:16302289pubmed:authorsCompleteYlld:pubmed
pubmed-article:16302289pubmed:pagination29-37lld:pubmed
pubmed-article:16302289pubmed:dateRevised2010-11-18lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:meshHeadingpubmed-meshheading:16302289...lld:pubmed
pubmed-article:16302289pubmed:year2006lld:pubmed
pubmed-article:16302289pubmed:articleTitleEffects of acute renal failure on the pharmacokinetics of DA-7867, a new oxazolidinone, in rats.lld:pubmed
pubmed-article:16302289pubmed:affiliationCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.lld:pubmed
pubmed-article:16302289pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16302289pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:16302289pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed