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dc.contributor.authorDios Pérez, Inmaculada de 
dc.contributor.authorGonzález Garcinuño, Álvaro 
dc.contributor.authorTabernero de Paz, Antonio 
dc.contributor.authorBlanco-López, Marcos
dc.contributor.authorGarcía Esteban, Juan Alberto 
dc.contributor.authorMoreno Rodilla, Vidal 
dc.contributor.authorCurto Diego, María Belén 
dc.contributor.authorPérez-Esteban, Patricia
dc.contributor.authorMartín del Valle, Eva María 
dc.date.accessioned2024-03-20T12:59:17Z
dc.date.available2024-03-20T12:59:17Z
dc.date.issued2023
dc.identifier.issn0928-0987
dc.identifier.urihttp://hdl.handle.net/10366/156820
dc.description.abstract[EN]This work proposes the development of a thermosensitive local drug release system based on Polaxamer 407, also known as Pluronic® F-127 (PF-127), Gellan Gum (GG) and the inclusion complex Sulfobutylated-β-cyclodextrin (CD) with Farnesol (FOH). Rheological properties of the hydrogels and their degradation were studied. According to the rheological results, a solution of 20% w/v of PF-127 forms a strong gel with a gelling temperature of about 25 C (storage modulus of 15,000 Pa). The addition of the GG increased the storage modulus (optimal concentration of 0.5 % w/v) twofold without modifying the gelling temperature. Moreover, including 0.5% w/v of GG also increased 6 times the degradation time of the hydrogel. Regarding the inclusion complex, the addition of free CD decreased the viscosity and the gel strength since polymer chains were included in CD cavity without affecting the gelling temperature. Contrarily, the inclusion complex CD-FOH did not significantly modify any property of the formulation because the FOH was hosted in the CD. Furthermore, a mathematical model was developed to adjust the degradation time. This model highlights that the addition of the GG decreases the number of released chains from the polymeric network (which coincides with an increase in the storage modulus) and that the free CD reduces the degradation rate, protecting the polymeric chains. Finally, FOH release was quantified with a specific device, that was designed and printed for this type of system, observing a sustainable drug release (similar to FOH aqueous solubility, 8 μ M) dependent on polymer degradation.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectDrug deliveryes_ES
dc.subjectThermosensitive gelses_ES
dc.subjectPluronic F-127es_ES
dc.subjectGellan gumes_ES
dc.titleDevelopment of a thermosensitive hydrogel based on Polaxamer 407 and gellan gum with inclusion complexes (Sulfobutylated-β-cyclodextrin–Farnesol) as a local drug delivery systemes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1016/j.ejps.2023.106618es_ES
dc.subject.unesco2302 Bioquímicaes_ES
dc.identifier.doi10.1016/j.ejps.2023.106618
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccesses_ES
dc.journal.titleEuropean Journal of Pharmaceutical Scienceses_ES
dc.volume.number191es_ES
dc.page.initial106618es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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