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dc.contributor.authorMuraguri GR.
dc.contributor.authorNgumi PN.
dc.contributor.authorWesonga D.
dc.contributor.authorNdungu SG.
dc.contributor.authorWanjohi John M.
dc.contributor.authorBang K.
dc.contributor.authorFoxb A.
dc.contributor.authorDunneb J.
dc.contributor.authorMcHardy N.
dc.date.accessioned2013-06-20T11:22:34Z
dc.date.available2013-06-20T11:22:34Z
dc.date.issued2006
dc.identifier.citationVolume 81, Issue 1, August 2006, Pages 119–126en
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S0034528805001724
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/36730
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/16289157
dc.description.abstractEast Coast fever, caused by the protozoan parasite Theileria parva, kills about 600,000 cattle annually in Africa. The hydroxynaphthoquinone compound buparvaquone (BPQ) is curative. Sixteen calves were infected with T. parva. On manifestation of disease symptoms, eight were injected with the original (pioneer) BPQ product and eight with a test product containing BPQ. All 16 calves were cured by one injection of 2.5 mg BPQ/kg bodyweight. The concentration of BPQ in blood plasma was monitored by HPLC. The mean observed Cmax of BPQ was 0.229 and 0.253 μg/mL of plasma, the mean observed time to reach this concentration (Tmax) was 2.62 and 2.12 h and the AUC (area under curve) was 4.785 and 4.156 μg h/mL, respectively, for the pioneer and test product. Considerable variations occurred in the plasma concentration of BPQ within each group. They showed no relationship with either clinical or parasitological parameters following treatment.en
dc.language.isoenen
dc.titleClinical efficacy and plasma concentrations of two formulations of buparvaquone in cattle infected with East Coast feveren
dc.typeArticleen
local.publisherDepartment of Chemistryen


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