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dc.contributor.authorKokwaro, GO
dc.contributor.authorTaylor, G
dc.date.accessioned2013-06-06T10:06:35Z
dc.date.available2013-06-06T10:06:35Z
dc.date.issued1990
dc.identifier.citationDrug Chem Toxicol. 1990;13(4):347-54.en
dc.identifier.urihttp://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/2279462
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/29153
dc.description.abstractBrain and plasma concentrations of oxaminiquine were determined following intravenous dosing (15 mg kg-1) in female Wistar rats. Maximum brain concentrations were achieved one hour after dosing and at all sampling times oxamniquine levels were higher in brain tissues compared to the corresponding plasma samples. It is concluded that the reported adverse neurological effects associated with the clinical use of oxaminiquine in man may be due to the passage of sufficiently large quantities of this drug into the CNS.en
dc.language.isoenen
dc.publisherUniversity of Nairobi.en
dc.titlePartitioning of oxaminiquine into brain tissue following intravenous administration to female Wistar ratsen
dc.typeArticleen
local.publisherDepartment of Pharmaceutics & Pharmacy Practice, Faculty of Pharmacy, College of Health Sciencesen


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