Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/35552
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dc.contributor.authorBharmoria, Pankajpt_PT
dc.contributor.authorBisht, Meenapt_PT
dc.contributor.authorGomes, Maria C.pt_PT
dc.contributor.authorMartins, Margaridapt_PT
dc.contributor.authorNeves, Márcia C.pt_PT
dc.contributor.authorMano, João F.pt_PT
dc.contributor.authorBdikin, Igorpt_PT
dc.contributor.authorCoutinho, João A. P.pt_PT
dc.contributor.authorVentura, Sónia P. M.pt_PT
dc.date.accessioned2023-01-02T11:09:01Z-
dc.date.available2023-01-02T11:09:01Z-
dc.date.issued2021-04-27-
dc.identifier.urihttp://hdl.handle.net/10773/35552-
dc.description.abstractThe sustainable cellular delivery of the pleiotropic drug curcumin encounters drawbacks related to its fast autoxidation at the physiological pH, cytotoxicity of delivery vehicles and poor cellular uptake. A biomaterial compatible with curcumin and with the appropriate structure to allow the correct curcumin encapsulation considering its poor solubility in water, while maintaining its stability for a safe release was developed. In this work, the biomaterial developed started by the preparation of an oil-in-water nanoemulsion using with a cytocompatible copolymer (Pluronic F 127) coated with a positively charged protein (gelatin), designed as G-Cur-NE, to mitigate the cytotoxicity issue of curcumin. These G-Cur-NE showed excellent capacity to stabilize curcumin, to increase its bio-accessibility, while allowing to arrest its autoxidation during its successful application as an anticancer agent proved by the disintegration of MDA-MB-231 breast cancer cells as a proof of concept.pt_PT
dc.language.isoengpt_PT
dc.publisherNature Researchpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50011%2F2020/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50011%2F2020/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/CEEC IND 2017/CEECIND%2F00383%2F2017%2FCP1459%2FCT0031/PTpt_PT
dc.relationERC-2014-ADG-669858pt_PT
dc.relationPOCI-01-0145-FEDER-022122pt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_CENTRO/SFRH%2FBD%2F122220%2F2016/PTpt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectAnimalspt_PT
dc.subjectAntineoplastic agentspt_PT
dc.subjectBreast neoplasmspt_PT
dc.subjectCell linept_PT
dc.subjectCurcuminpt_PT
dc.subjectDrug carrierspt_PT
dc.subjectDrug delivery systemspt_PT
dc.subjectDrug stabilitypt_PT
dc.subjectEmulsionspt_PT
dc.subjectFemalept_PT
dc.subjectFibroblastspt_PT
dc.subjectGelatinpt_PT
dc.subjectHumanspt_PT
dc.subjectMicept_PT
dc.subjectNanostructurespt_PT
dc.subjectOlive Oilpt_PT
dc.subjectPoloxamerpt_PT
dc.subjectWaterpt_PT
dc.subjectPhytogenicpt_PT
dc.subjectTumorpt_PT
dc.titleProtein-olive oil-in-water nanoemulsions as encapsulation materials for curcumin acting as anticancer agent towards MDA-MB-231 cellspt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.issue1pt_PT
degois.publication.titleScientific reportspt_PT
degois.publication.volume11pt_PT
dc.identifier.doi10.1038/s41598-021-88482-3pt_PT
dc.identifier.essn2045-2322pt_PT
dc.identifier.articlenumber9099pt_PT
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