Farmacología de los azoles

Azole antifungals have different pharmacokinetic characteristics: complete oral absorption for Voriconazole, and to a lesser extent for fluconazole. The absorption of posaconazole and itraconazole increases with food intake. All of them have high tissue distribution with low plasma concentrations, e...

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Detalles Bibliográficos
Autores: Azanza, J.R. (José Ramón)|||/items/230f0ec2-020f-4a5e-954f-d488b5480300, Garcia-Quetglas, E. (Emilio)|||/items/01e522cd-1940-41f7-b71f-ace7cfdf7b4a, Sadaba-Díaz-de-Rada, M.B. (María Belén)|||/items/729be158-ad4f-4ca5-8431-fa54abff5f8a
Tipo de recurso: artículo
Fecha de publicación:2007
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:español
OAI Identifier:oai:dadun.unav.edu:10171/22724
Acceso en línea:https://hdl.handle.net/10171/22724
Access Level:acceso abierto
Palabra clave:Pharmacology
Posaconazole
Itraconazole
Farmacología clínica
Descripción
Sumario:Azole antifungals have different pharmacokinetic characteristics: complete oral absorption for Voriconazole, and to a lesser extent for fluconazole. The absorption of posaconazole and itraconazole increases with food intake. All of them have high tissue distribution with low plasma concentrations, especially low in the case of posaconazole and itraconazole. Posaconazole and itraconazole have high plasmatic protein binding and consequently both have a very low free fraction. Elimination of azole antifungals is through a metabolic pathway with CYP450 isoenzymes, and has a non linear pharmacokinetics with a high risk of interation with other drugs since azoles have the ability of CYP450 isoenzymes inhibition. Possibly the parameter that defines more precisely their efficacy is AUIC with an optimum value near 20, although cut-off values must be defined since some azoles may have difficulty to reach this value.