Pregled bibliografske jedinice broj: 687150
Development of mucoadhesive wafers loaded with econazole-cyclodextrin complexes for treatment of oral candidiadis
Development of mucoadhesive wafers loaded with econazole-cyclodextrin complexes for treatment of oral candidiadis // Programme and Abstract
Pisa: APGI & ADRITELF, 2013. (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Development of mucoadhesive wafers loaded with econazole-cyclodextrin complexes for treatment of oral candidiadis
Autori
Mennini, Natascia ; Jug, Mario ; Furlanetto, Sandra ; Mura, Paola
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Programme and Abstract
/ - Pisa : APGI & ADRITELF, 2013
Skup
3rd Conference Innovation in Drug Delivery Advances in Local Drug Delivery
Mjesto i datum
Pisa, Italija, 22.09.2013. - 25.09.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
econazole nitrate; buccal delivery; mucoadhesion; quality by design
Sažetak
The aim of this work was the development of an oral topical drug delivery system of econazole, endowed with mucoadhesive properties, able to assure a prolonged in situ drug release, thus allowing prevention and more efficient treatment of the Candida infection. Different kinds of hydrogels based on amidated pectins and carboxymethyl cellulose (CMC) were prepared, loaded with econazole nitrate (ECO) at 0.1% w/w, added as coground product with sulfobutylether-β-cyclodextrin and citric acid, due to its optimised dissolution properties. After freezing, the hydrogels were lyophilized, to obtain wafers for oral application. Experimental design methodologies were applied to optimize the wafer composition, maximizing its mucoadhesive properties, evaluated "ex vivo" in terms of residence time and adhesive strength to excised porcine mucosa. Drug release studies in simulated saliva were performed on the optimized formulation by using an open-compartment dissolution apparatus to maintain sink conditions. The best composition of the wafer, resulted from the analysis of the response surface plots, was: amidated pectin 7.2 % (w/w) and CMC 5.2% (w/w). The experimental values of adhesive strength (28.4 0.04 g/cm2) and residence time (88.10.1 min) given by the optimized formulation were very close to the predicted values, demonstrating the validity of the applied model. The optimized wafers showed an appropriate and controlled drug release during the observed residence time on the mucosa surface. Combination of amidated pectin and CMC, in suitable proportions, allowed preparation of mucoadhesive wafers able to form mucoadhesive hydrogels on contact with saliva and to ensure a prolonged residence time and release of the drug in situ.
Izvorni jezik
Engleski
Znanstvena područja
Farmacija