dc.date.accessioned2022-01-18T19:26:46Z
dc.date.available2022-01-18T19:26:46Z
dc.date.created2022-01-18T19:26:46Z
dc.date.issued2012
dc.identifierhttps://hdl.handle.net/20.500.12866/10857
dc.identifierhttps://doi.org/10.1016/j.fct.2012.07.023
dc.description.abstractOxfendazole (OFZ) is efficacious for porcine cysticercosis at 30mg/kg. OFZ is not registered to be used at this dose. The assessment of the OFZ and metabolites [(fenbendazole sulphone (FBZSO2), fenbendazole (FBZ)] plasma pharmacokinetic and tissue residue profiles after its oral administration to pigs and the withdrawal period for human consumption were reported. Forty-eight pigs allocated into two groups received OFZ (30mg/kg) orally as a commercial (CF) or as experimental formulation (SMF). Samples (blood, muscle, liver, kidney and fat) were collected over 30days post-treatment and analyzed by HPLC. OFZ was the main compound recovered in plasma, followed by FBZSO2 and low FBZ concentrations. OFZ AUC0-LOQ (209.9±33.9μg·h/ml) and Cmax (5.40±0.65μg/ml) parameters for the CF tended to be higher than those for the SMF (AUC0-LOQ: 159.4±18.3μgh/ml, Cmax: 3.80±0.35μg/ml). The highest total residue (OFZ+FBZSO2+FBZ) concentrations were quantified in liver, followed by kidney, muscle and fat tissue. FBZSO2 residue levels were the highest found in muscle (0.68±0.39μg/g) and fat (0.69±0.39μg/g). In liver and kidney the highest residues corresponded to FBZ (5.29±4.36μg/g) and OFZ (2.86±0.75μg/g), respectively. A withdrawal time of 17days post-treatment was established before tissues are delivered for human consumption.
dc.languageeng
dc.publisherElsevier
dc.relationFood and Chemical Toxicology
dc.relation1873-6351
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectMale
dc.subjectControlled Study
dc.subjectAnimal Experiment
dc.subjectFood Intake
dc.subjectBlood Sampling
dc.subjectAnthelmintics
dc.subjectCysticercosis
dc.subjectSwine Diseases
dc.subjectBenzimidazoles
dc.subjectDose-Response Relationship Drug
dc.subjectArea Under Curve
dc.subjectHigh Performance Liquid Chromatography
dc.subjectLiver
dc.subjectKidney
dc.subjectAdipose Tissue
dc.subjectDrug Residues
dc.subjectFenbendazole Sulphone
dc.subject|Pharmacokinetics
dc.titleA high oxfendazole dose to control porcine cysticercosis: Pharmacokinetics and tissue residue profiles
dc.typeinfo:eu-repo/semantics/article


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