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Effect of mucoadhesive polymers on the in vitro performance of insulin-loaded silica nanoparticles: Interactions with mucin and biomembrane models

dc.contributor.authorAndreani, Tatiana
dc.contributor.authorMiziara, Leonardo [UNESP]
dc.contributor.authorLorenzón, Esteban N. [UNESP]
dc.contributor.authorSouza, Ana Luiza R. de [UNESP]
dc.contributor.authorKiill, Charlene P. [UNESP]
dc.contributor.authorFangueiro, Joana F.
dc.contributor.authorGarcia, Maria L.
dc.contributor.authorGremião, Palmira D. [UNESP]
dc.contributor.authorSilva, Amelia M.
dc.contributor.authorSouto, Eliana B.
dc.contributor.institutionUniversity of Tras-os Montes e Alto Douro (UTAD)
dc.contributor.institutionCentre for Research and Technology of Agro-Environmental and Biological Sciences (CITAB)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Fernando Pessoa (UFP)
dc.contributor.institutionBarcelona University
dc.contributor.institutionFaculty of Pharmacy, University of Coimbra (FFUC)
dc.contributor.institutionUniversity of Coimbra
dc.date.accessioned2015-10-21T20:19:39Z
dc.date.available2015-10-21T20:19:39Z
dc.date.issued2015-06-01
dc.description.abstractThe present paper focuses on the development and characterization of silica nanoparticles (SiNP) coated with hydrophilic polymers as mucoadhesive carriers for oral administration of insulin. SiNP were prepared by sol-gel technology under mild conditions and coated with different hydrophilic polymers, namely, chitosan, sodium alginate or poly(ethylene glycol) (PEG) with low and high molecular weight (PEG 6000 and PEG 20000) to increase the residence time at intestinal mucosa. The mean size and size distribution, association efficiency, insulin structure and insulin thermal denaturation have been determined. The mean nanoparticle diameter ranged from 289 nm to 625 nm with a PI between 0.251 and 0.580. The insulin association efficiency in SiNP was recorded above 70%. After coating, the association efficiency of insulin increased up to 90%, showing the high affinity of the protein to the hydrophilic polymer chains. Circular dichroism (CD) indicated that no conformation changes of insulin structure occurred after loading the peptide into SiNP. Nano-differential scanning calorimetry (nDSC) showed that SiNP shifted the insulin endothermic peak to higher temperatures. The influence of coating on the interaction of nanoparticles with dipalmitoylphosphatidylcholine (DPPC) biomembrane models was also evaluated by nDSC. The increase of AH values suggested a strong association of non-coated SiNP and those PEGylated nanopartides coated with DPPC polar heads by forming hydrogen bonds and/or by electrostatic interaction. The mucoadhesive properties of nanoparticles were examined by studying the interaction with mucin in aqueous solution. SiNP coated with alginate or chitosan showed high contact with mucin. On the other hand, non-coated SiNP and PEGylated SiNP showed lower interaction with mucin, indicating that these nanopartides can interdiffuse across mucus network. The results of the present work provide valuable data in assessing the in vitro performance of insulin-loaded SiNP coated with mucoadhesive polymers. (C) 2015 Elsevier B.V. All rights reserved.en
dc.description.affiliationDepartment of Biology and Environment, University of Tras-os Montes e Alto Douro, UTAD, Quinta de Prados, P-5001-801 Vila Real, Portugal
dc.description.affiliationCentre for Research and Technology of Agro-Environmental and Biological Sciences, CITAB, UTAD, Quinta de Prados, P-5001-801 Vila Real, Portugal
dc.description.affiliationResearch Centre for Biomedicine (CEBIMED), Fernando Pessoa University (UFP), Praça 9 de Abril, 349, P-4249-004 Porto, Portugal f Department of Physical Chemistry, Faculty of Pharmacy, Barcelona University, Av. Joan XXIII s/n, 08028 Barcelona, Spain
dc.description.affiliationDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra (FFUC), Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, Portugal
dc.description.affiliationCenter for Neuroscience and Cell Biology & Institute for Biomedical Imaging and Life Sciences (CNC-IBILI), University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, Portugal.
dc.description.affiliationUnespDepartment of Biochemistry and Chemical Technology, Institute of Chemistry, UNESP, Araraquara, São Paulo, Brazil
dc.description.affiliationUnespDepartment of Pharmaceutical Sciences, UNESP-Universidade Estadual Paulista, Rodovia Araraquara-Jau, Km. 01, Araraquara, São Paulo, Brazil.
dc.description.sponsorshipFundacao para a Ciencia e Tecnologia (FCT, Portugal)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipEuropean Union Funds (FEDER/COMPETE)
dc.description.sponsorshipIdFCT, Portugal: SFRH/BD/60640/2009
dc.description.sponsorshipIdFCT, Portugal: SFRH/BD/80335/2011
dc.description.sponsorshipIdFEDER/COMPETE: FCOMP-01-0124-FEDER-022696
dc.description.sponsorshipIdFAPESP: 2012/10174-3
dc.description.sponsorshipIdFAPESP: 140758/2011-9
dc.format.extent118-126
dc.identifierhttp://www.sciencedirect.com/science/article/pii/S0939641115001605
dc.identifier.citationEuropean Journal Of Pharmaceutics And Biopharmaceutics. Amsterdam: Elsevier Science Bv, v. 93, p. 118-126, 2015.
dc.identifier.doi10.1016/j.ejpb.2015.03.027
dc.identifier.issn0939-6411
dc.identifier.lattes9129780536724256
dc.identifier.urihttp://hdl.handle.net/11449/129079
dc.identifier.wosWOS:000356554000012
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofEuropean Journal Of Pharmaceutics And Biopharmaceutics
dc.relation.ispartofjcr4.491
dc.relation.ispartofsjr1,342
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectSilica nanoparticlesen
dc.subjectMucoadhesionen
dc.subjectInsulinen
dc.subjectOral deliveryen
dc.subjectBiomembranesen
dc.subjectThermal denaturationen
dc.titleEffect of mucoadhesive polymers on the in vitro performance of insulin-loaded silica nanoparticles: Interactions with mucin and biomembrane modelsen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.advisor.lattes9129780536724256
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentBioquímica e Tecnologia - IQpt

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