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dc.contributor.authorEnshaei, Hamidreza
dc.contributor.authorMolina, Brenda G.
dc.contributor.authorValle Mendoza, Luis Javier del
dc.contributor.authorEstrany Coda, Francesc
dc.contributor.authorArnan, Carme
dc.contributor.authorPuiggalí Bellalta, Jordi
dc.contributor.authorSaperas Plana, Núria
dc.contributor.authorAlemán Llansó, Carlos
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament d'Enginyeria Química
dc.date.accessioned2019-09-26T08:19:59Z
dc.date.available2020-06-21T00:26:44Z
dc.date.issued2019-01-01
dc.identifier.citationEnshaei, H. [et al.]. Scaffolds for sustained release of ambroxol hydrochloride, a pharmacological Chaperone that Increases the Activity of Misfolded ß-Glucocerebrosidase. "Macromolecular bioscience (Internet)", 1 Gener 2019, vol. 19, núm. 8, p. 1900130.
dc.identifier.issn1616-5195
dc.identifier.urihttp://hdl.handle.net/2117/168717
dc.description.abstractAmbroxol is a pharmacological chaperone (PC) for Gaucher disease that increases lysosomal activity of misfolded ß-glucocerebrosidase (GCase) while displaying a safe toxicological profile. In this work, different poly(e-caprolactone) (PCL)-based systems are developed to regulate the sustained release of small polar drugs in physiological environments. For this purpose, ambroxol is selected as test case since the encapsulation and release of PCs using polymeric scaffolds have not been explored yet. More specifically, ambroxol is successfully loaded in electrospun PCL microfibers, which are subsequently coated with additional PCL layers using dip-coating or spin-coating. The time needed to achieve 80% release of loaded ambroxol increases from ˜15 min for uncoated fibrous scaffolds to 3 days and 1 week for dip-coated and spin-coated systems, respectively. Furthermore, it is proven that the released drug maintains its bioactivity, protecting GCase against induced thermal denaturation
dc.format.extent12 p.
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Spain
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectÀrees temàtiques de la UPC::Enginyeria química
dc.subject.lcshPolymers
dc.subject.lcshBiomedical materials
dc.titleScaffolds for sustained release of ambroxol hydrochloride, a pharmacological Chaperone that Increases the Activity of Misfolded ß-Glucocerebrosidase
dc.typeArticle
dc.subject.lemacPolímers
dc.subject.lemacMaterials biomèdics
dc.contributor.groupUniversitat Politècnica de Catalunya. PSEP - Polimers Sintètics: Estructura i Propietats. Polimers Biodegradables
dc.contributor.groupUniversitat Politècnica de Catalunya. IMEM-BRT- Innovation in Materials and Molecular Engineering - Biomaterials for Regenerative Therapies
dc.contributor.groupUniversitat Politècnica de Catalunya. MACROM - Cristal·lografia, Estructura i Funció de Macromolècules Biològiques
dc.identifier.doi10.1002/mabi.201900130
dc.description.peerreviewedPeer Reviewed
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/abs/10.1002/mabi.201900130
dc.rights.accessOpen Access
local.identifier.drac25501943
dc.description.versionPostprint (author's final draft)
local.citation.authorEnshaei, H.; Molina, B.; del Valle, LJ.; Estrany, F.; Arnan, C.; Puiggali, J.; Saperas, N.; Aleman, C.
local.citation.publicationNameMacromolecular bioscience (Internet)
local.citation.volume19
local.citation.number8
local.citation.startingPage1900130:1
local.citation.endingPage190013012


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