Pharmacokinetics of menbutone after intravenous and intramuscular administration to sheep

[EN] Menbutone is a drug currently approved in several European Union (EU) countries to treat digestive disorders in different animal species. The objective of this study was to establish the pharmacokinetic parameters resulting from intravenous (IV) and intramuscular (IM) administration of this dru...

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Detalles Bibliográficos
Autores: Díez Láiz, Raquel, Diez Liébana, María José, García Viéitez, Juan José, Rodríguez Lago, José Manuel, López Cadenas, Cristina, Fernández Martínez, María Nélida, Sierra Vega, Matilde, Sahagún Prieto, Ana María
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2022
País:España
Institución:Universidad de León
Repositorio:BULERIA. Repositorio Institucional de la Universidad de León
OAI Identifier:oai:buleria.unileon.es:10612/17757
Acceso en línea:https://www.frontiersin.org/articles/10.3389/fvets.2022.980818/full
https://hdl.handle.net/10612/17757
Access Level:acceso abierto
Palabra clave:Farmacología
Veterinaria
Choleretic
Intramuscular
Intravenous
Menbutone
Pharmacokinetics
Sheep
3109 Ciencias Veterinarias
3109.08 Farmacología
Descripción
Sumario:[EN] Menbutone is a drug currently approved in several European Union (EU) countries to treat digestive disorders in different animal species. The objective of this study was to establish the pharmacokinetic parameters resulting from intravenous (IV) and intramuscular (IM) administration of this drug in sheep. Menbutone was administered to 12 animals at the dose of 10 mg/kg for both IV and IM routes. Plasma samples were collected up to 24 h (15 points, IV route; 14 points, IM route). Concentrations were determined using high-performance liquid chromatography with photodiode-array (PDA) detection, following a method validated according to the EMEA/CHMP/EWP/192217/2009 guideline. Pharmacokinetic data were analyzed by non-compartmental methods. After IV administration, a total clearance (Cl) of 63.6 ± 13.6 mL/h/kg, a volume of distribution at steady-state (Vss) of 259.6±52.7mL/kg, and an elimination half-life (t½l) of 6.08 ± 2.48 h were calculated. After IM administration, menbutone peak plasma concentration (Cmax) was 18.8 ± 1.9μg/mL, the time to reach Cmax (tmax) 3.75 ± 0.45 h, the mean absorption time (MAT) 3.31 ± 1.36 h, and the fraction of dose absorbed (F) 103.1 ± 23.0 %. The results obtained indicate that menbutone absorption after IM administration is quick and complete.