Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106356
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dc.contributor.authorCollado-González, Mar-
dc.contributor.authorFerreri, M. Cristina-
dc.contributor.authorFreitas, Alessandra-
dc.contributor.authorSantos, Ana Cláudia-
dc.contributor.authorFerreira, Nuno Ricardo Esteves-
dc.contributor.authorCarissimi, Guzmán-
dc.contributor.authorSequeira, Joana A. D.-
dc.contributor.authorDíaz Baños, F. Guillermo-
dc.contributor.authorVillora, Gloria-
dc.contributor.authorVeiga, Francisco-
dc.contributor.authorRibeiro, António-
dc.date.accessioned2023-03-31T08:40:37Z-
dc.date.available2023-03-31T08:40:37Z-
dc.date.issued2020-01-15-
dc.identifier.issn1660-3397pt
dc.identifier.urihttps://hdl.handle.net/10316/106356-
dc.description.abstractPolyelectrolyte nanocomposites rarely reach a stable state and aggregation often occurs. Here, we report the synthesis of nanocomposites for the oral delivery of insulin composed of alginate, dextran sulfate, poly-(ethylene glycol) 4000, poloxamer 188, chitosan, and bovine serum albumin. The nanocomposites were obtained by Ca2+-induced gelation of alginate followed by an electrostatic-interaction process among the polyelectrolytes. Chitosan seemed to be essential for the final size of the nanocomposites and there was an optimal content that led to the synthesis of nanocomposites of 400-600 nm hydrodynamic size. The enhanced stability of the synthesized nanocomposites was assessed with LUMiSizer after synthesis. Nanocomposite stability over time and under variations of ionic strength and pH were assessed with dynamic light scattering. The rounded shapes of nanocomposites were confirmed by scanning electron microscopy. After loading with insulin, analysis by HPLC revealed complete drug release under physiologically simulated conditions.pt
dc.description.sponsorshipThis work has been partially supported from the European Commission (FEDER/ERDF) and the Spanish Ministry of Economy and Competitiveness (MINECO) (ref CTQ2017-87708-R) and by the Fundación Séneca del Centro de Coordinación de la Investigación de la Región de Murcia under projects 20977/PI/18 and by the Nils Coordinated Mobility under grant 012-ABEL-CM-2014A. Mar Collado-González acknowledges the fellowship for postdoctoral training (20381/PD/17) funded by the Consejería de Empleo, Universidades y Empresa de la Comunidad Autónoma de la Región de Murcia (CARM), through the Fundación Séneca de la Región de Murcia and for the support from the University of Murcia for stays abroad of young researchers and doctoral students in the action lines of Campus Mare Nostrum (R273/2016). Alessandra R. Freitas acknowledges support from the Brazilian National Council for Scientific and Technological Development (BolsistaCNPq-Brasil). Ana Cláudia Santos acknowledges support from the Portuguese Foundation for Science and Technology (FCT; SFRH/BD/109261/2015). Joana A. D. Sequeira acknowledges support from the Portuguese Foundation for Science and Technology and Tecnimede-S.A. for the grant (PD/BDE/135148/2017).-
dc.language.isoengpt
dc.publisherMDPIpt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectchitosanpt
dc.subjectalginate polysaccharide nanocompositept
dc.subjectstabilitypt
dc.subjectLUMiSizerpt
dc.subject.meshAdministration, Oralpt
dc.subject.meshAlginatespt
dc.subject.meshChitosanpt
dc.subject.meshDrug Carrierspt
dc.subject.meshDrug Delivery Systemspt
dc.subject.meshGelspt
dc.subject.meshInsulinpt
dc.subject.meshNanocompositespt
dc.subject.meshPolyethylene Glycolspt
dc.subject.meshPolysaccharidespt
dc.subject.meshSerum Albumin, Bovinept
dc.subject.meshStatic Electricitypt
dc.titleComplex Polysaccharide-Based Nanocomposites for Oral Insulin Deliverypt
dc.typearticle-
degois.publication.firstPage55pt
degois.publication.issue1pt
degois.publication.titleMarine Drugspt
dc.peerreviewedyespt
dc.identifier.doi10.3390/md18010055pt
degois.publication.volume18pt
dc.date.embargo2020-01-15*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
item.openairetypearticle-
item.cerifentitytypePublications-
item.languageiso639-1en-
crisitem.author.researchunitInstitute for Research and Innovation in Health Sciences-
crisitem.author.orcid0000-0003-2710-6000-
crisitem.author.orcid0000-0002-1041-0068-
crisitem.author.orcid0000-0002-1399-8944-
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