Stability of a per os ciprofloxacin formulation ESTABILIDAD DE UNA FORMULACION ORAL DE CIPROFLOXACINA

dc.creatorChavez,
dc.creatorBriones,
dc.creatorArancibia, Verónica
dc.date.accessioned2019-01-29T14:53:03Z
dc.date.available2019-01-29T14:53:03Z
dc.date.created2019-01-29T14:53:03Z
dc.date.issued1993
dc.identifierActa Farmaceutica Bonaerense, Volumen 12, Issue 3, 2018, Pages 149-154
dc.identifier03262383
dc.identifierhttp://repositorio.uchile.cl/handle/2250/161181
dc.description.abstractA stability study of a ciprofloxacin tablet formulation was performed. For the stability study, samples of tablets were stored during a six month period both at room conditions and under 37°C of relative humidity; after this time degradation products were determined and weight variation, desintegration time, hardness, friability and dissolution kinetics were evaluated. The ANOVA method, and the Dunnet Test (p < 0.01) were used for the statistical analysis. Good stability tablet characteristics in some galenical properties observed after storing the tablets at 37°C and 75% humidity did not affect their dissolution properties.
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceActa Farmaceutica Bonaerense
dc.subjectciprofloxacin
dc.subjectdosage form development
dc.subjectstability studies
dc.titleStability of a per os ciprofloxacin formulation ESTABILIDAD DE UNA FORMULACION ORAL DE CIPROFLOXACINA
dc.typeArtículos de revistas


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