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Pharmacokinetics and bioavailability of meloxicam in rainbow trout (Oncorhynchus mykiss) broodstock following intravascular, intramuscular, and oral administrations

dc.contributor.authorCorum, Orhan
dc.contributor.authorTerzi, Ertugrul
dc.contributor.authorDurna Corum, Duygu
dc.contributor.authorUney, Kamil
dc.date.accessioned2026-01-04T15:56:32Z
dc.date.issued2021-11-14
dc.description.abstractAbstractThe pharmacokinetics and bioavailability of meloxicam were investigated after single intravascular (IV), intramuscular (IM), and oral dose of 1 mg/kg in rainbow trout broodstock at 11 ± 1.2°C. A total of 36 healthy rainbow trout (Oncorhynchus mykiss) broodstock weighing 1.40 ± 0.26 kg was used for the investigation. Plasma concentrations of meloxicam were measured with high‐performance liquid chromatography‐ultraviolet detection, and pharmacokinetic parameters were calculated by non‐compartmental analysis. The elimination half‐life for IV, IM, and oral routes was 3.63, 4.55, and 2.95 h, respectively. The IV route for meloxicam showed the total clearance of 0.05 L/h/kg and volume of distribution at a steady state of 0.20 L/kg. The peak plasma concentration was 2.97 μg/ml for the IM route and 0.84 μg/ml for the oral route. The bioavailability was 78.45% for the IM route and 21.48% for the oral route. Meloxicam following IM and oral administration displayed short t1/2ʎz. The short t1/2ʎz could be an advantage for the short‐term use in acute conditions. The IM route with the good bioavailability can be preferred for the treatment of various conditions. However, developing new oral formulations with the good bioavailability for meloxicam is necessary to minimize stress and trauma through minimal handling in rainbow trout broodstock.
dc.description.urihttps://doi.org/10.1111/jvp.13031
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/34778976
dc.description.urihttps://dx.doi.org/10.1111/jvp.13031
dc.identifier.doi10.1111/jvp.13031
dc.identifier.eissn1365-2885
dc.identifier.endpage219
dc.identifier.issn0140-7783
dc.identifier.openairedoi_dedup___::0c44e6498f18c2b16cbed703a3ea1883
dc.identifier.orcid0000-0003-3168-2510
dc.identifier.orcid0000-0003-2811-6497
dc.identifier.orcid0000-0003-1567-991x
dc.identifier.orcid0000-0002-8674-4873
dc.identifier.pubmed34778976
dc.identifier.scopus2-s2.0-85119284555
dc.identifier.startpage213
dc.identifier.urihttps://hdl.handle.net/20.500.12597/39166
dc.identifier.volume45
dc.identifier.wos000718202100001
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofJournal of Veterinary Pharmacology and Therapeutics
dc.rightsCLOSED
dc.subjectOncorhynchus mykiss
dc.subjectAdministration, Oral
dc.subjectAnimals
dc.subjectBiological Availability
dc.subjectMeloxicam
dc.subjectInjections, Intramuscular
dc.subjectHalf-Life
dc.titlePharmacokinetics and bioavailability of meloxicam in rainbow trout (Oncorhynchus mykiss) broodstock following intravascular, intramuscular, and oral administrations
dc.typeArticle
dspace.entity.typePublication
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A total of 36 healthy rainbow trout (<jats:italic>Oncorhynchus mykiss</jats:italic>) broodstock weighing 1.40 ± 0.26 kg was used for the investigation. Plasma concentrations of meloxicam were measured with high‐performance liquid chromatography‐ultraviolet detection, and pharmacokinetic parameters were calculated by non‐compartmental analysis. The elimination half‐life for IV, IM, and oral routes was 3.63, 4.55, and 2.95 h, respectively. The IV route for meloxicam showed the total clearance of 0.05 L/h/kg and volume of distribution at a steady state of 0.20 L/kg. The peak plasma concentration was 2.97 μg/ml for the IM route and 0.84 μg/ml for the oral route. The bioavailability was 78.45% for the IM route and 21.48% for the oral route. Meloxicam following IM and oral administration displayed short t<jats:sub>1/2ʎz</jats:sub>. The short t<jats:sub>1/2ʎz</jats:sub> could be an advantage for the short‐term use in acute conditions. 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local.import.sourceOpenAire
local.indexed.atWOS
local.indexed.atScopus
local.indexed.atPubMed

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