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dc.date.accessioned 2010-11-08T17:46:17Z
dc.date.available 2010-11-08T03:00:00Z
dc.date.issued 2010 es
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/8033
dc.description.abstract A new reversible thermosensitive drug delivery system was designed and prepared by using chitosan and glycerophosphate with or without poly (ethylene glycol) and used as an a carrier for the Miconazole nitrate, an antifungal agent used in the treatment of vaginal fungal infections. The optimum preparative condition was investigated and it was found that the formulation was solution below or at room temperature with low viscosity, and at 37 ºC, transformed to a non-flowing hydrogel. The formulation was evaluated for gelation temperature, gelation time, drug-polymer compatibility, drug content uniformity, viscosity, in vitro drug release profile and stability studies. The release of loaded Miconazole nitrate from the hydrogel was significantly sustained and the effect of PEG-4000 and Glycerophosphate concentration on release rate was observed. The results showed that the formed hydrogel is a controlled release carrier, which will favour its use as an improved vaginal drug delivery system. es
dc.format.extent 1093-1099 es
dc.language es es
dc.subject chitosan; glycerophosphate; PEG-4000; thermosensitive gel; vaginal drug delivery es
dc.title Formulation development and evaluation of thermosensitive gel for vaginal drug delivery es
dc.type Articulo es
sedici.identifier.uri http://www.latamjpharm.org/resumenes/29/7/LAJOP_29_7_1_6.pdf es
sedici.creator.person Bhat, Sudeendra R. es
sedici.creator.person Shivakumar, Hosakote G. es
sedici.subject.materias Farmacia es
sedici.description.fulltext false es
mods.originInfo.place Colegio de Farmacéuticos de la Provincia de Buenos Aires es
sedici.subtype Articulo es
sedici.description.peerReview peer-review es
sedici2003.identifier ARG-FARM-ART-0000001520 es
sedici.relation.journalTitle Latin American Journal of Pharmacy es
sedici.relation.journalVolumeAndIssue vol. 29, no. 7 es


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