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pubmed-article:8210701pubmed:abstractTextA single dose pharmacokinetic study with modified human Interleukin-1 Beta (IL-1 beta or DuP 118) was performed by injecting 5 micrograms/kg of drug into the jugular vein of three beagle dogs. Serial 5-ml plasma samples were removed from the dogs over a 120-minute period. DuP 118 plasma levels were measured using a sandwich ELISA technique capable of measuring concentrations ranging from 0.25 to 2 ng/ml with accuracy and precision constraints of less than +/- 20% variability. DuP 118 stored at -20 degrees C in dog plasma was stable for at least 1 month. Pharmacokinetic parameters were determined for the three dogs by standard model independent or non-compartmental methods. DuP 118 was rapidly distributed in the dog. The volume of distribution was approximately two-fold higher than the total body water of a lean dog. The terminal half-life was short, less than 30 minutes. Within approximately an hour after dosing, DuP 118 plasma levels were reduced 20-fold and were below the quantifiable limit of the assay.lld:pubmed
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pubmed-article:8210701pubmed:statusMEDLINElld:pubmed
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pubmed-article:8210701pubmed:issn0034-5164lld:pubmed
pubmed-article:8210701pubmed:authorpubmed-author:PieniaszekH...lld:pubmed
pubmed-article:8210701pubmed:authorpubmed-author:GrayJ EJElld:pubmed
pubmed-article:8210701pubmed:authorpubmed-author:KongY MYMlld:pubmed
pubmed-article:8210701pubmed:authorpubmed-author:NewtonRRlld:pubmed
pubmed-article:8210701pubmed:authorpubmed-author:PetermanVVlld:pubmed
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pubmed-article:8210701pubmed:volume81lld:pubmed
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pubmed-article:8210701pubmed:pagination233-41lld:pubmed
pubmed-article:8210701pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:8210701pubmed:year1993lld:pubmed
pubmed-article:8210701pubmed:articleTitleELISA determination and preliminary pharmacokinetics of modified human rIL-1 beta in dogs.lld:pubmed
pubmed-article:8210701pubmed:affiliationDrug Metabolism and Pharmacokinetics Section, Du Pont Merck Pharmaceutical Company, Newark, DE 19714.lld:pubmed
pubmed-article:8210701pubmed:publicationTypeJournal Articlelld:pubmed