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Pharmacokinetics of cefquinome after single and repeated subcutaneous administrations in sheep

dc.contributor.authorCorum, Orhan
dc.contributor.authorCorum, Duygu Durna
dc.contributor.authorEr, Ayse
dc.contributor.authorUney, Kamil
dc.date.accessioned2026-01-04T12:42:05Z
dc.date.issued2019-02-04
dc.description.abstractAbstractThe purpose of this study was to determine the pharmacokinetics of cefquinome (CFQ) following single and repeated subcutaneous (SC) administrations in sheep. Six clinically healthy, 1.5 ± 0.2 years sheep were used for the study. In pharmacokinetic study, the crossover design in three periods was performed. The withdrawal interval between the study periods was 15 days. In first period, CFQ (Cobactan, 2.5%) was administered by an intravenous (IV) bolus (3 sheep) and SC (3 sheep) injections at 2.5 mg/kg dose. In second period, the treatment administration was repeated via the opposite administration route. In third period, CFQ was administrated subcutaneously to each sheep (n = 6) at a dose of 2.5 mg/kg q. 24 hr for 5 days. Plasma concentrations of CFQ were measured using the HPLC‐UV method. Pharmacokinetic parameters were calculated using non‐compartmental methods. The elimination half‐life and mean residence time of CFQ after the single SC administration were longer than IV administration (p < 0.05). Bioavailability (F%) of CFQ following the single SC administration was 123.51 ± 11.54%. The area under the curve (AUC0‐∞) and peak concentration following repeated doses (last dose) were higher than those observed after the first dose (p < 0.05). CFQ accumulated after repeated SC doses. CFQ can be given via SC at a dose of 2.5 mg/kg every 24 hr for the treatment of infections caused by susceptible pathogens, which minimum inhibitory concentration is ≤1.0 μg/ml in sheep.
dc.description.urihttps://doi.org/10.1111/jvp.12750
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/30719732
dc.description.urihttps://dx.doi.org/10.1111/jvp.12750
dc.description.urihttps://hdl.handle.net/20.500.12395/38081
dc.identifier.doi10.1111/jvp.12750
dc.identifier.eissn1365-2885
dc.identifier.endpage653
dc.identifier.issn0140-7783
dc.identifier.openairedoi_dedup___::567fd7dc39f5908a5eb01c103dd85d45
dc.identifier.orcid0000-0003-3168-2510
dc.identifier.orcid0000-0003-1567-991x
dc.identifier.orcid0000-0002-8674-4873
dc.identifier.pubmed30719732
dc.identifier.scopus2-s2.0-85061200433
dc.identifier.startpage647
dc.identifier.urihttps://hdl.handle.net/20.500.12597/37228
dc.identifier.volume42
dc.identifier.wos000501034000010
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofJournal of Veterinary Pharmacology and Therapeutics
dc.rightsOPEN
dc.subjectsheep
dc.subjectSheep
dc.subjectBacteria
dc.subjectInjections, Subcutaneous
dc.subjectMicrobial Sensitivity Tests
dc.subjectDrug Administration Schedule
dc.subjectAnti-Bacterial Agents
dc.subjectCephalosporins
dc.subjectArea Under Curve
dc.subjectAnimals
dc.subjectsubcutaneous
dc.subjectbioavailability
dc.subjectpharmacokinetics
dc.subjectcefquinome
dc.subjectHalf-Life
dc.subject.sdg2. Zero hunger
dc.subject.sdg3. Good health
dc.titlePharmacokinetics of cefquinome after single and repeated subcutaneous administrations in sheep
dc.typeArticle
dspace.entity.typePublication
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Good health"},"provenance":null},{"subject":{"scheme":"FOS","value":"0403 veterinary science"},"provenance":null},{"subject":{"scheme":"FOS","value":"03 medical and health sciences"},"provenance":null},{"subject":{"scheme":"keyword","value":"Area Under Curve"},"provenance":null},{"subject":{"scheme":"keyword","value":"Animals"},"provenance":null},{"subject":{"scheme":"keyword","value":"subcutaneous"},"provenance":null},{"subject":{"scheme":"keyword","value":"bioavailability"},"provenance":null},{"subject":{"scheme":"keyword","value":"pharmacokinetics"},"provenance":null},{"subject":{"scheme":"keyword","value":"cefquinome"},"provenance":null},{"subject":{"scheme":"keyword","value":"Half-Life"},"provenance":null}],"mainTitle":"Pharmacokinetics of cefquinome after single and repeated subcutaneous administrations in sheep","subTitle":null,"descriptions":["<jats:title>Abstract</jats:title><jats:p>The purpose of this study was to determine the pharmacokinetics of cefquinome (<jats:styled-content style=\"fixed-case\">CFQ</jats:styled-content>) following single and repeated subcutaneous (<jats:styled-content style=\"fixed-case\">SC</jats:styled-content>) administrations in sheep. Six clinically healthy, 1.5 ± 0.2 years sheep were used for the study. In pharmacokinetic study, the crossover design in three periods was performed. The withdrawal interval between the study periods was 15 days. In first period, <jats:styled-content style=\"fixed-case\">CFQ</jats:styled-content> (Cobactan, 2.5%) was administered by an intravenous (<jats:styled-content style=\"fixed-case\">IV</jats:styled-content>) bolus (3 sheep) and <jats:styled-content style=\"fixed-case\">SC</jats:styled-content> (3 sheep) injections at 2.5 mg/kg dose. In second period, the treatment administration was repeated via the opposite administration route. In third period, <jats:styled-content style=\"fixed-case\">CFQ</jats:styled-content> was administrated subcutaneously to each sheep (<jats:italic>n</jats:italic> = 6) at a dose of 2.5 mg/kg q. 24 hr for 5 days. Plasma concentrations of CFQ were measured using the <jats:styled-content style=\"fixed-case\">HPLC</jats:styled-content>‐<jats:styled-content style=\"fixed-case\">UV</jats:styled-content> method. Pharmacokinetic parameters were calculated using non‐compartmental methods. The elimination half‐life and mean residence time of <jats:styled-content style=\"fixed-case\">CFQ</jats:styled-content> after the single <jats:styled-content style=\"fixed-case\">SC</jats:styled-content> administration were longer than <jats:styled-content style=\"fixed-case\">IV</jats:styled-content> administration (<jats:italic>p </jats:italic>&lt; 0.05). Bioavailability (<jats:italic>F</jats:italic>%) of <jats:styled-content style=\"fixed-case\">CFQ</jats:styled-content> following the single <jats:styled-content style=\"fixed-case\">SC</jats:styled-content> administration was 123.51 ± 11.54%. 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