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dc.contributor.author Cabrera-Barjas, Gustavo
dc.contributor.author Becherán, Liliam
dc.contributor.author Valdés, Oscar
dc.contributor.author Giordano, Ady
dc.contributor.author Segura-del Río, Rodrigo
dc.contributor.author Bravo-Arrepol, Gastón
dc.contributor.author Durán-Lara, Esteban F.
dc.contributor.author Cea, Juan
dc.contributor.author Berg, Alex
dc.contributor.author Castaños, Johana
dc.contributor.author Rodríguez-Llamazares, Saddys
dc.contributor.author Fuentes, Gastón
dc.contributor.author Katsarov, Plamen
dc.contributor.author Lukova, Paolina
dc.contributor.author Delattre, Cédric
dc.date.accessioned 2024-09-12T03:36:32Z
dc.date.available 2024-09-12T03:36:32Z
dc.date.issued 2023-10-10
dc.identifier.issn 0014-3057
dc.identifier.uri https://repositorio.uss.cl/handle/uss/11235
dc.description Funding Information: In memory of our dear colleague and friend, Patricia Bernabé Galloway, Ph.D., who performed part of this research until COVID-19 took her life. The authors also acknowledge the finantial support of ANID grant PIA/APOYO CCTE AFB170007, ACE210016 (G.C-B.; S. R-L., A.B.); CIPA CONICYT Regional GORE BIO BIO R17A10003, ACE210016 (S.R.L.; G.C-B.); ANID BASAL FB210015 CENAMAD (G.C-B., A.B.); INNOVA ALTA TECNOLOGIA 19IAT-112022 (G.C-B., J.C., A.B.); CORFO 22CVID-206836 (S.R-L); ANID FONDECYT REGULAR 1221609 (G.C-B.) and 1210107 (O.V.). and to Fondequip EQM 190179 (R.S., G.C-B). Funding Information: This research was funded by ANID grant PIA/APOYO CCTE AFB170007, ACE210016 (G.C-B.; S. R-L., A.B.); CIPA CONICYT Regional GORE BIO BIO R17A10003, ACE210016 (S.R.L.; G.C-B.); ANID BASAL FB210015 CENAMAD (G.C-B., A.B.); INNOVA ALTA TECNOLOGIA 19IAT-112022 (G.C-B., J.C., A.B.); CORFO 22CVID-206836 (S.R-L); ANID FONDECYT REGULAR 1221609 (G.C-B.) and 1210107 (O.V.). Funding Information: This research was funded by ANID grant PIA/APOYO CCTE AFB170007 , ACE210016 (G.C-B.; S. R-L., A.B.); CIPA CONICYT Regional GORE BIO BIO R17A10003 , ACE210016 (S.R.L.; G.C-B.); ANID BASAL FB210015 CENAMAD (G.C-B., A.B.); INNOVA ALTA TECNOLOGIA 19IAT-112022 (G.C-B., J.C., A.B.); CORFO 22CVID-206836 (S.R-L); ANID FONDECYT REGULAR 1221609 (G.C-B.) and 1210107 (O.V.). Publisher Copyright: © 2023 Elsevier Ltd
dc.description.abstract Overuse of antibiotic drugs usually leads to the further development of resistance to targeted bacteria. In this context, a controlled release system could be a solution to achieve higher drug efficiency without overdosing and drug resistance. In this work, nanocomposite films based on chitosan (CHI) reinforced with cellulose nanofibrils (CNF) for antibiotic release were prepared and characterized. Several nanocomposite films containing vancomycin hydrochloride and different amounts of CNF (5, 10, and 20 wt%) were prepared by the solvent casting method. Spectroscopic (FTIR), thermal (TG), morphological (SEM), mechanical, and swelling analyses of the films were performed to study the effect of nanofibers content on the nanocomposite properties. A good dispersion of CNF and the model drug was observed in the CHI matrix. FTIR spectroscopy confirmed the interaction between the film components (CNF and CHI). Film swelling capacity decreased with an increase of CNF content in the film formulation, whereas stiffness and tensile strength of the film increased. In addition, vancomycin release at pH = 7.4 was studied, and it was observed that controlled slower release could be achieved by tuning the CNF content in the chitosan film. The results confirm that these films could be useful for pharmaceutical purposes where the controlled release of drugs is required. en
dc.language.iso eng
dc.relation.ispartof vol. 197 Issue: Pages:
dc.source European Polymer Journal
dc.title Effect of cellulose nanofibrils on vancomycin drug release from chitosan nanocomposite films en
dc.type Artículo
dc.identifier.doi 10.1016/j.eurpolymj.2023.112371
dc.publisher.department Facultad de Ciencias para el Cuidado de la Salud


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