Comparative bioavailability of two digoxin formulations: determination in human plasma by microparticle enzyme immunoassay
The present study was performed to compare the bioavailability of two digoxin 0.25 mg tablet formulation in 30 volunteers of both sexes. The study was conducted open with randomized two period crossover design and a three-week washout period. Plasma samples were obtained over a 144 h interval. Digox...
Guardado en:
| Autores principales: | Junior, Eduardo A., Duarte, Luciana F., Vanunci, Moisés L. P., Silva, Lara C., Pereira, Renata, Calafatti, Silvana, Junior, José P. |
|---|---|
| Formato: | Articulo Comunicacion |
| Lenguaje: | Inglés |
| Publicado: |
2011
|
| Materias: | |
| Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/8288 http://www.latamjpharm.org/resumenes/30/6/LAJOP_30_6_2_7.pdf |
| Aporte de: |
Ejemplares similares
-
Bioequivalence Study of Deferiprone In Healthy Pakistani Volunteers
por: Abbas, Mateen, et al.
Publicado: (2012) -
Study of comparative bioavailability among two formulations containing hydroxyzine hydrochloride in healthy volunteers
after a single dose administration
por: Junior, Eduardo A., et al.
Publicado: (2011) -
Modelo farmacocinético flujo-dependiente : Aplicación clínica a la digoxina
por: Fagiolino, Pietro, et al.
Publicado: (1996) -
Determination of Escitalopram in Human Plasma by High Performance Liquid Chromatography-Tandem Mass Spectrometry
por: Sousa, Carlos E.M., et al.
Publicado: (2012) -
Bioequivalence test applied to a new lamivudine/zidovudine combined formulation tablet
por: Souza, Jacqueline de, et al.
Publicado: (2009)