Pharmacokinetic model of florfenicol in tilapia (Oreochromis niloticus) subjected to different rearing temperatures

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The aim of this study was to develop a pharmacokinetic model of florfenicol in plasma of tilapia (Oreochromis niloticus) subjected to different rearing temperatures to estimate the plasma concentration of the protocols indicated in the package inserts of florfenicol products authorized in Brazil. Fo...

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Detalles Bibliográficos
Autores: Ramos Tameirão, Emanuely, Marcos Rubim, Fernando, Alexsandra Felix, Larissa, Wamser Fonseca Gonzaga, Lucas, de Mello Brandão, Humberto, David Solis Murgas, Luis, Ferrante, Marcos
Formato: artículo
Fecha de Publicación:2022
Institución:Universidad Nacional Mayor de San Marcos
Repositorio:Revistas - Universidad Nacional Mayor de San Marcos
Lenguaje:español
OAI Identifier:oai:ojs.csi.unmsm:article/22433
Enlace del recurso:https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/22433
Nivel de acceso:acceso abierto
Materia:antibiotic therapy
pharmacometry
fish farming
dosage regimen
terapia antibiótica
farmacometría
piscicultura
régimen de dosis
Descripción
Sumario:The aim of this study was to develop a pharmacokinetic model of florfenicol in plasma of tilapia (Oreochromis niloticus) subjected to different rearing temperatures to estimate the plasma concentration of the protocols indicated in the package inserts of florfenicol products authorized in Brazil. For this, a pharmacokinetic model was created from previously published data on the plasma concentration of florfenicol in Nile tilapia subjected to different temperatures. The construction of the pharmacokinetic model was carried out with the Lixoft® Monolix 2020R1 program, based on the plasma pharmacokinetic data of florfenicol found in the literature. Plasma concentrations of florfenicol were estimated from treatments with doses of 10, 15 and 20 mg/kg administered every 24 hours for 10 days, at temperatures of 18, 21, 26 and 30 °C, using the Lixoft Simulx 2020 program®. The absorption latency time (Tlag) and clearance (Cl) parameters showed a positive correlation with temperature, while the absorption constant (Ka) showed a negative correlation. Likewise, animals kept at 30 °C have a median mobile plasma concentration of approximately half that of animals raised at 18°C and treated with the same doses. Increasing doses, on the other hand, resulted in an approximately two-fold increase in median plasma concentration. The proposed model allowed quantifying the impact of temperature on pharmacokinetic parameters, in addition to estimating plasma concentrations of florfenicol for tilapia at different rearing temperatures.
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