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Effect of castration procedure on the pharmacokinetics of meloxicam in goat kids

dc.contributor.authorTekeli, Ibrahim Ozan
dc.contributor.authorTurk, Erdinc
dc.contributor.authorDurna Corum, Duygu
dc.contributor.authorCorum, Orhan
dc.contributor.authorUney, Kamil
dc.date.accessioned2026-01-04T14:08:45Z
dc.date.issued2020-05-18
dc.description.abstractAbstractThe aim of this study was to determine the changes in the pharmacokinetics of meloxicam in goat kids who were castrated following the administration of xylazine. Six goat kids were used for the study. The study was performed in two periods according to a longitudinal study, with a 15‐day washout period between periods. In the first period (Control group), 1 mg/kg meloxicam was administered by i.v. route to kids. In the second period (Castration group), the kids were sedated with 0.3 mg/kg xylazine and castration was performed following meloxicam administration. Plasma meloxicam concentration was analyzed using HPLC‐UV, and pharmacokinetic parameters were calculated by noncompartmental model. In the control group following the administration of meloxicam, mean elimination half‐life (t1/2ʎz), area under the concentration–time curve (AUC0−∞), total body clearance (ClT), and volume of distribution at steady‐state (Vdss) were 13.50 ± 0.62 hr, 41.10 ± 2.86 hr µg/ml, 24.43 ± 1.75 ml hr−1 kg−1, and 0.45 ± 0.03 L/kg, respectively. In the castration group, the t1/2ʎz of meloxicam prolonged, AUC0−∞ increased, and ClT and Vdss decreased. In conclusion, the excretion of meloxicam from the body slowed and the t1/2ʎz was prolonged in the castrated goat kids following xylazine administration. However, there is a need to determine the pharmacodynamics of meloxicam in castrated goat kids.
dc.description.urihttps://doi.org/10.1111/jvp.12872
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/32420638
dc.description.urihttps://dx.doi.org/10.1111/jvp.12872
dc.identifier.doi10.1111/jvp.12872
dc.identifier.eissn1365-2885
dc.identifier.endpage434
dc.identifier.issn0140-7783
dc.identifier.openairedoi_dedup___::1f1d118423231a276754c2c5f8645d51
dc.identifier.orcid0000-0002-6845-2279
dc.identifier.orcid0000-0003-1567-991x
dc.identifier.orcid0000-0003-3168-2510
dc.identifier.orcid0000-0002-8674-4873
dc.identifier.pubmed32420638
dc.identifier.scopus2-s2.0-85084844948
dc.identifier.startpage429
dc.identifier.urihttps://hdl.handle.net/20.500.12597/37972
dc.identifier.volume43
dc.identifier.wos000533346700001
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofJournal of Veterinary Pharmacology and Therapeutics
dc.rightsCLOSED
dc.subjectMale
dc.subjectArea Under Curve
dc.subjectGoats
dc.subjectAnti-Inflammatory Agents, Non-Steroidal
dc.subjectAnimals
dc.subjectLongitudinal Studies
dc.subjectMeloxicam
dc.subjectOrchiectomy
dc.subjectHalf-Life
dc.subject.sdg3. Good health
dc.titleEffect of castration procedure on the pharmacokinetics of meloxicam in goat kids
dc.typeArticle
dspace.entity.typePublication
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In the control group following the administration of meloxicam, mean elimination half‐life (<jats:italic>t</jats:italic><jats:sub>1/2</jats:sub><jats:italic><jats:sub>ʎz</jats:sub></jats:italic>), area under the concentration–time curve (AUC<jats:sub>0−∞</jats:sub>), total body clearance (Cl<jats:sub>T</jats:sub>), and volume of distribution at steady‐state (<jats:italic>V</jats:italic><jats:sub>dss</jats:sub>) were 13.50 ± 0.62 hr, 41.10 ± 2.86 hr µg/ml, 24.43 ± 1.75 ml hr<jats:sup>−1</jats:sup> kg<jats:sup>−1</jats:sup>, and 0.45 ± 0.03 L/kg, respectively. In the castration group, the <jats:italic>t</jats:italic><jats:sub>1/2</jats:sub><jats:italic><jats:sub>ʎz</jats:sub></jats:italic> of meloxicam prolonged, AUC<jats:sub>0−∞</jats:sub> increased, and Cl<jats:sub>T</jats:sub> and <jats:italic>V</jats:italic><jats:sub>dss</jats:sub> decreased. 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local.import.sourceOpenAire
local.indexed.atWOS
local.indexed.atScopus
local.indexed.atPubMed

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