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Pharmacokinetics of intravenous and intramuscular danofloxacin in red-eared slider turtles (Trachemys scripta elegans).

dc.contributor.authorCorum, Orhan
dc.contributor.authorCorum, Duygu Durna
dc.contributor.authorAltan, Feray
dc.contributor.authorEr, Ayse
dc.contributor.authorCetin, Gul
dc.contributor.authorUney, Kamil
dc.date.accessioned2026-01-04T12:25:23Z
dc.date.issued2018-11-17
dc.description.abstractThis study aimed to investigate the pharmacokinetics of danofloxacin in red-eared slider turtle (Trachemys scripta elegans) following a single intravenous (IV) and intramuscular (IM) administrations of 6 mg/kg, using a two-way crossover study with 30-day washout period. Eight clinically healthy red-eared slider turtle weighing 410-600 g (mean 490 g) were used for the study. Danofloxacin concentrations were measured using the reversed-phase high-performance liquid chromatography. The plasma concentration-time data were evaluated by a non-compartmental method. After IV administration, the elimination half-life (t1/2 ʎ z), mean residence time (MRT0-∞), area under the concentration-time curve (AUC0-∞), volume of distribution at steady state and total body clearance in plasma were 24.17 hr, 30.64 hr, 143.31 hr·μg/ml, 1.29 l/kg and 0.04 l/hr/kg, respectively. Following IM administration, t1/2ʎz, MRT0-∞AUC0-∞,peak concentration (Cmax), time to reach Cmax, and bioavailability in plasma were 32.00 hr, 41.15 hr, 198.23 hr·μg/ml, 8.75 μg/ml, 1.5 hr and 139.89%, respectively. Danofloxacin has clinically superior pharmacokinetic properties, including the complete IM absorption, slow elimination and wide volume of distribution in redeared slider turtles. However, further pharmacokinetics/pharmacodynamics studies are necessary for the treatment of diseases caused by susceptible bacteria with known minimum inhibitory concentration values in red-eared slider turtles.
dc.description.abstractPMID:30853667
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/30853667
dc.description.urihttp://dx.doi.org/10.1292/jvms.18-0609
dc.description.urihttps://avesis.deu.edu.tr/publication/details/b53c9189-9aff-4c1d-86de-e7d5beadc9e8/oai
dc.description.urihttps://avesis.deu.edu.tr/publication/details/b3c123e9-49b8-446a-9552-49d767b620cf/oai
dc.description.urihttps://www.jstage.jst.go.jp/article/jvms/81/5/81_18-0609/_article
dc.description.urihttps://hdl.handle.net/11468/7582
dc.description.urihttps://doi.org/10.1292/jvms.18-0609
dc.description.urihttps://hdl.handle.net/20.500.12395/38083
dc.identifier.issn1347-7439
dc.identifier.openairepmid_dedup__::b9f15c4a949a1a751eec64422a8cbcf9
dc.identifier.urihttps://hdl.handle.net/20.500.12597/37036
dc.identifier.volume81
dc.language.isoeng
dc.publisherThe Japanese Society of Veterinary Science
dc.relation.ispartofThe Journal of veterinary medical science
dc.rightsOPEN
dc.subjectPharmacology
dc.subjectCross-Over Studies
dc.subjectBioavailability
dc.subjectRed-eared slider turtles
dc.subjectBiological Availability
dc.subjectDanofloxacin
dc.subjectInjections, Intramuscular
dc.subjectTurtles
dc.subjectAnti-Infective Agents
dc.subjectred-eared slider turtles
dc.subjectInjections, Intravenous
dc.subjectdanofloxacin
dc.subjectAnimals
dc.subjectPharmacokinetics
dc.subjectbioavailability
dc.subjectpharmacokinetics
dc.subjectFluoroquinolones
dc.subject.sdg3. Good health
dc.titlePharmacokinetics of intravenous and intramuscular danofloxacin in red-eared slider turtles (Trachemys scripta elegans).
dc.typeArticle
dspace.entity.typePublication
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Eight clinically healthy red-eared slider turtle weighing 410-600 g (mean 490 g) were used for the study. Danofloxacin concentrations were measured using the reversed-phase high-performance liquid chromatography. The plasma concentration-time data were evaluated by a non-compartmental method. After IV administration, the elimination half-life (t1/2 ʎ z), mean residence time (MRT0-∞), area under the concentration-time curve (AUC0-∞), volume of distribution at steady state and total body clearance in plasma were 24.17 hr, 30.64 hr, 143.31 hr·μg/ml, 1.29 l/kg and 0.04 l/hr/kg, respectively. Following IM administration, t1/2ʎz, MRT0-∞AUC0-∞,peak concentration (Cmax), time to reach Cmax, and bioavailability in plasma were 32.00 hr, 41.15 hr, 198.23 hr·μg/ml, 8.75 μg/ml, 1.5 hr and 139.89%, respectively. Danofloxacin has clinically superior pharmacokinetic properties, including the complete IM absorption, slow elimination and wide volume of distribution in redeared slider turtles. 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