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Pharmacokinetics and bioavailability of danofloxacin in chukar partridge (Alectoris chukar) following intravenous, intramuscular, subcutaneous, and oral administrations

dc.contributor.authorCorum, Orhan
dc.contributor.authorDurna Corum, Duygu
dc.contributor.authorAtik, Orkun
dc.contributor.authorEser Faki, Hatice
dc.contributor.authorAltan, Feray
dc.contributor.authorUney, Kamil
dc.date.accessioned2026-01-04T12:25:46Z
dc.date.issued2018-11-25
dc.description.abstractAbstractThe aim of the present study was to determine the pharmacokinetics (PKs) and bioavailability of danofloxacin in chukar partridge (Alectoris chukar) following intravenous (IV), intramuscular (IM), subcutaneous (SC), and oral (PO) administrations at a dose of 10 mg/kg. A total of eight clinically healthy chukar partridges weighing 480 ± 45 g were used for the investigation. The study was performed in a crossover design (2 × 2 × 2 × 2) with a 15‐day washout period between two administrations in four periods. The plasma concentrations of danofloxacin were determined using reversed‐phase high‐performance liquid chromatography. Noncompartmental PK parameters were also estimated. No local or systemic adverse drug effects were observed in any of the chukar partridges. The mean elimination half‐life ranged between 8.18 and 12.08 hr and differed statistically among administration routes. The mean peak plasma concentrations of danofloxacin following IM, SC, and PO administrations were 8.05, 9.58, and 3.39 μg/ml at 0.5, 1, and 4 hr, respectively. Following IM, SC, and PO administrations, the mean bioavailability was 86.33%, 134.40%, and 47.62%, respectively. The mean total clearance and volume of distribution at steady‐state following IV administration were 0.13 L hr−1 kg−1 and 0.96 L/kg, respectively. These data, including favorable PKs and the absence of adverse drug effects, suggest that danofloxacin is a useful antibiotic in chukar partridges.
dc.description.urihttps://doi.org/10.1111/jvp.12737
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/30474236
dc.description.urihttps://dx.doi.org/10.1111/jvp.12737
dc.description.urihttps://avesis.deu.edu.tr/publication/details/3b8b0421-a50f-42f9-8be6-291febcdaa8a/oai
dc.description.urihttps://avesis.deu.edu.tr/publication/details/29a63cf4-db67-4618-b1b0-678b71f402f0/oai
dc.description.urihttps://hdl.handle.net/11468/17716
dc.description.urihttps://hdl.handle.net/20.500.12395/38080
dc.identifier.doi10.1111/jvp.12737
dc.identifier.eissn1365-2885
dc.identifier.endpage213
dc.identifier.issn0140-7783
dc.identifier.openairedoi_dedup___::4972bd5dfb040f23893e388ba5b5461e
dc.identifier.orcid0000-0003-3168-2510
dc.identifier.orcid0000-0003-1567-991x
dc.identifier.orcid0000-0003-2411-7492
dc.identifier.orcid0000-0002-9017-763x
dc.identifier.orcid0000-0002-8674-4873
dc.identifier.pubmed30474236
dc.identifier.scopus2-s2.0-85057225795
dc.identifier.startpage207
dc.identifier.urihttps://hdl.handle.net/20.500.12597/37040
dc.identifier.volume42
dc.identifier.wos000460077600009
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofJournal of Veterinary Pharmacology and Therapeutics
dc.rightsOPEN
dc.subjectBioavailability
dc.subjectInjections, Subcutaneous
dc.subjectchukar partridge
dc.subjectAdministration, Oral
dc.subjectBiological Availability
dc.subjectChukar Partridge
dc.subjectDanofloxacin
dc.subjectInjections, Intramuscular
dc.subjectAnti-Bacterial Agents
dc.subjectInjections, Intravenous
dc.subjectdanofloxacin
dc.subjectAnimals
dc.subjectPharmacokinetics
dc.subjectGalliformes
dc.subjectbioavailability
dc.subjectpharmacokinetics
dc.subjectChromatography, High Pressure Liquid
dc.subjectFluoroquinolones
dc.subjectHalf-Life
dc.subject.sdg3. Good health
dc.titlePharmacokinetics and bioavailability of danofloxacin in chukar partridge (Alectoris chukar) following intravenous, intramuscular, subcutaneous, and oral administrations
dc.typeArticle
dspace.entity.typePublication
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Good health"},"provenance":null},{"subject":{"scheme":"FOS","value":"0403 veterinary science"},"provenance":null},{"subject":{"scheme":"keyword","value":"Injections, Intravenous"},"provenance":null},{"subject":{"scheme":"keyword","value":"danofloxacin"},"provenance":null},{"subject":{"scheme":"keyword","value":"Animals"},"provenance":null},{"subject":{"scheme":"keyword","value":"Pharmacokinetics"},"provenance":null},{"subject":{"scheme":"keyword","value":"Galliformes"},"provenance":null},{"subject":{"scheme":"keyword","value":"bioavailability"},"provenance":null},{"subject":{"scheme":"keyword","value":"pharmacokinetics"},"provenance":null},{"subject":{"scheme":"keyword","value":"Chromatography, High Pressure Liquid"},"provenance":null},{"subject":{"scheme":"keyword","value":"Fluoroquinolones"},"provenance":null},{"subject":{"scheme":"keyword","value":"Half-Life"},"provenance":null}],"mainTitle":"Pharmacokinetics and bioavailability of danofloxacin in chukar partridge (<i>Alectoris chukar</i>) following intravenous, intramuscular, subcutaneous, and oral administrations","subTitle":null,"descriptions":["<jats:title>Abstract</jats:title><jats:p>The aim of the present study was to determine the pharmacokinetics (<jats:styled-content style=\"fixed-case\">PK</jats:styled-content>s) and bioavailability of danofloxacin in chukar partridge (<jats:italic>Alectoris chukar</jats:italic>) following intravenous (<jats:styled-content style=\"fixed-case\">IV</jats:styled-content>), intramuscular (<jats:styled-content style=\"fixed-case\">IM</jats:styled-content>), subcutaneous (<jats:styled-content style=\"fixed-case\">SC</jats:styled-content>), and oral (<jats:styled-content style=\"fixed-case\">PO</jats:styled-content>) administrations at a dose of 10 mg/kg. A total of eight clinically healthy chukar partridges weighing 480 ± 45 g were used for the investigation. The study was performed in a crossover design (2 × 2 × 2 × 2) with a 15‐day washout period between two administrations in four periods. The plasma concentrations of danofloxacin were determined using reversed‐phase high‐performance liquid chromatography. Noncompartmental <jats:styled-content style=\"fixed-case\">PK</jats:styled-content> parameters were also estimated. No local or systemic adverse drug effects were observed in any of the chukar partridges. The mean elimination half‐life ranged between 8.18 and 12.08 hr and differed statistically among administration routes. The mean peak plasma concentrations of danofloxacin following <jats:styled-content style=\"fixed-case\">IM</jats:styled-content>,<jats:styled-content style=\"fixed-case\"> SC</jats:styled-content>, and <jats:styled-content style=\"fixed-case\">PO</jats:styled-content> administrations were 8.05, 9.58, and 3.39 μg/<jats:styled-content style=\"fixed-case\">ml</jats:styled-content> at 0.5, 1, and 4 hr, respectively. Following <jats:styled-content style=\"fixed-case\">IM</jats:styled-content>,<jats:styled-content style=\"fixed-case\"> SC</jats:styled-content>, and <jats:styled-content style=\"fixed-case\">PO</jats:styled-content> administrations, the mean bioavailability was 86.33%, 134.40%, and 47.62%, respectively. The mean total clearance and volume of distribution at steady‐state following <jats:styled-content style=\"fixed-case\">IV</jats:styled-content> administration were 0.13 L hr<jats:sup>−1</jats:sup> kg<jats:sup>−1</jats:sup> and 0.96 L/kg, respectively. 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