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pubmed-article:11393731pubmed:dateCreated2001-6-6lld:pubmed
pubmed-article:11393731pubmed:abstractTextAn improved high-performance liquid chromatographic method has been developed to measure human plasma concentrations of the analgesic nonsteroidal anti-inflammatory drug ketorolac for use in pharmacokinetic studies. Samples were prepared for analysis by solid-phase extraction using Bond-Elut PH columns, with nearly complete recovery of both ketorolac and the internal standard tolmetin. The two compounds were separated on a Radial-Pak C18 column using a mobile phase consisting of water-acetonitrile-1.0 mol/l dibutylamine phosphate (pH 2.5) (30:20:1) and detected at a UV wavelength of 313 nm. Using only 250 microl of plasma, the standard curve was linear from 0.05 to 10.0 microg/ml.lld:pubmed
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pubmed-article:11393731pubmed:authorpubmed-author:WangZZlld:pubmed
pubmed-article:11393731pubmed:authorpubmed-author:AvramM JMJlld:pubmed
pubmed-article:11393731pubmed:authorpubmed-author:DsidaR MRMlld:pubmed
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pubmed-article:11393731pubmed:pagination383-6lld:pubmed
pubmed-article:11393731pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:11393731pubmed:year2001lld:pubmed
pubmed-article:11393731pubmed:articleTitleDetermination of ketorolac in human plasma by reversed-phase high-performance liquid chromatography using solid-phase extraction and ultraviolet detection.lld:pubmed
pubmed-article:11393731pubmed:affiliationDepartment of Anesthesiology, Northwestern University Medical School, Chicago, IL 60611, USA.lld:pubmed
pubmed-article:11393731pubmed:publicationTypeJournal Articlelld:pubmed
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