Pharmacokinetic study of propofol in horses
Pharmacokinetic study of propofol in horses
Authors
Lüders Post, Carlos
Ahumada, F.
Baroni, E.E.
Saavedra, I.
Zambucetti, R.
Ahumada, F.
Baroni, E.E.
Saavedra, I.
Zambucetti, R.
Authors
Date
2012-02-24
Datos de publicación:
10.4067/S0301-732X1998000100009
Keywords
Equinos - Farmacocinética - Farmacodinamia - Propofol
Collections
Abstract
Se estudian las características farmacocinéticas de propofol en 6 caballos. Se determinaron parámetros farmacocinéticos de propofol cuantificando sus concentraciones sanguíneas en función del tiempo por HPLC, tras su administración de 2.4 mg/kg por vía endovenosa al grupo de animales. Los datos de concentración se interpretaron por un modelo abierto de 2 compartimentos, obteniéndose, entre otros, los valores de t1/2a, t1/2b,Vdc, Vdss, Vdb, Cltotaly MRT. Las variables farmacodinámicas se encuentran acordes a la disposición cinética de este fármaco. El análisisde los parámetros farmacocinéticos del propofol indica que éste posee una rápida y pronta distribución a los tejidos y una rápida eliminación del organismo. El propofol se presenta como una alternativa anestésica factible de ser incorporada dentro de un protocolo anestésico en caballos. Los parámetros farmacocinéticos obtenidos contribuyen para una correcta dosificación ya sea para mantener un estado de anestesia por infusión continua o por inyecciones repetidas
Pharmacokinetic variables of propofol were studied in 6 horses. Blood concentration of propofol at different times, after a single dose of 2.4mg/kg bw, was determined by HPLC. An open two compartment model was used to evaluate blood concentrations of propofol. Values of t1/2a,t1/2b, Vdc, Vdss,Vdb, Cltotal y MRT were obtained.The pharmacodynamic values show a narrow relationship with the pharmacokinetic disposition of this drug. Propofol s pharmacokinetic disposition presented a rapid distribution and removal from organic tissues. It is concluded that propofol is an alternative to be considered in anaesthetic protocolsin horses, and the pharmacokinetic variables presented contribute to determinethe appropriate dose to be given
Pharmacokinetic variables of propofol were studied in 6 horses. Blood concentration of propofol at different times, after a single dose of 2.4mg/kg bw, was determined by HPLC. An open two compartment model was used to evaluate blood concentrations of propofol. Values of t1/2a,t1/2b, Vdc, Vdss,Vdb, Cltotal y MRT were obtained.The pharmacodynamic values show a narrow relationship with the pharmacokinetic disposition of this drug. Propofol s pharmacokinetic disposition presented a rapid distribution and removal from organic tissues. It is concluded that propofol is an alternative to be considered in anaesthetic protocolsin horses, and the pharmacokinetic variables presented contribute to determinethe appropriate dose to be given