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Design of innovative biocompatible cellulose nanostructures for the delivery and sustained release of curcumin

dc.contributor.authorCasanova, Francisca
dc.contributor.authorPereira, Carla F.
dc.contributor.authorRibeiro, Alessandra B.
dc.contributor.authorCosta, Eduardo M.
dc.contributor.authorFreixo, Ricardo
dc.contributor.authorCastro, Pedro M.
dc.contributor.authorFernandes, João C.
dc.contributor.authorPintado, Manuela
dc.contributor.authorRamos, Óscar L.
dc.date.accessioned2023-03-28T17:15:36Z
dc.date.available2023-03-28T17:15:36Z
dc.date.issued2023-03-18
dc.description.abstractPoor aqueous solubility, stability and bioavailability of interesting bioactive compounds is a challenge in the development of bioactive formulations. Cellulose nanostructures are promising and sustainable carriers with unique features that may be used in enabling delivery strategies. In this work, cellulose nanocrystals (CNC) and cellulose nanofibers were investigated as carriers for the delivery of curcumin, a model liposoluble compound. Nanocellulose modification with the surfactant cetyltrimethylammonium bromide (CTAB), tannic acid and decylamine (TADA), and by TEMPO-mediated oxidation were also tested and compared. The carrier materials were characterized in terms of structural properties and surface charge, while the delivery systems were evaluated for their encapsulation and release properties. The release profile was assessed in conditions that mimic the gastric and intestinal fluids, and cytotoxicity studies were performed in intestinal cells to confirm safe application. Modification with CTAB and TADA resulted in high curcumin encapsulation efficiencies of 90 and 99%, respectively. While no curcumin was released from TADA-modified nanocellulose in simulated gastrointestinal conditions, CNC-CTAB allowed for a curcumin-sustained release of ca. 50% over 8 h. Furthermore, the CNC-CTAB delivery system showed no cytotoxic effects on Caco-2 intestinal cells up to 0.125 g/L, meaning that up to this concentration the system is safe to use. Overall, the use of the delivery systems allowed for the reduction in the cytotoxicity associated with higher curcumin concentrations, highlighting the potential of nanocellulose encapsulation systems.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.3390/pharmaceutics15030981pt_PT
dc.identifier.eid85152053380
dc.identifier.issn1999-4923
dc.identifier.pmcPMC10051681
dc.identifier.pmid36986845
dc.identifier.urihttp://hdl.handle.net/10400.14/40734
dc.identifier.wos000960239700001
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectNanocellulosept_PT
dc.subjectCurcuminpt_PT
dc.subjectDelivery systemspt_PT
dc.subjectSustained releasept_PT
dc.subjectCytotoxicitypt_PT
dc.titleDesign of innovative biocompatible cellulose nanostructures for the delivery and sustained release of curcuminpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue3pt_PT
oaire.citation.titlePharmaceuticspt_PT
oaire.citation.volume15pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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