<?xml version='1.0' encoding='utf-8'?>
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>S. M. Plakas</dc:contributor>
  <dc:creator>G. R. Stehly</dc:creator>
  <dc:date>1992</dc:date>
  <dc:description>The pharmacokinetics, tissue distribution, and metabolism of 1-naphthol were examined in the channel  catfish (Ictalurus punctatus ). After oral dosing, peak plasma concentrations of 1-naphthol occurred at 1 hr;  parent compound made up less than 15% of the total radioactivity, and the bioavailability was 32%. Plasma  protein binding was 92% and was independent of concentration. 1-Naphthol and metabolites were rapidly  eliminated from the tissues after oral dosing.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:language>en</dc:language>
  <dc:publisher>U.S. Food and Drug Administration</dc:publisher>
  <dc:title>Disposition of 1-naphthol in the channel catfish (Ictalurus punctatus)</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>