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Combining Coaxial Electrospinning and 3D Printing: Design of Biodegradable Bilayered Membranes with Dual Drug Delivery Capability for Periodontitis Treatment

dc.contributor.authorDos Santos, Danilo M.
dc.contributor.authorDe Annunzio, Sarah R. [UNESP]
dc.contributor.authorCarmello, Juliana C. [UNESP]
dc.contributor.authorPavarina, Ana C. [UNESP]
dc.contributor.authorFontana, Carla R. [UNESP]
dc.contributor.authorCorrea, Daniel S.
dc.contributor.institutionEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2022-04-29T08:38:00Z
dc.date.available2022-04-29T08:38:00Z
dc.date.issued2022-01-17
dc.description.abstractPeriodontitis is a chronic inflammatory disease that can lead to significant destruction of tooth-supporting tissues, compromising dental function and patient's health. Although the currently employed treatment approaches can limit the advance of the disease, the development of multifunctional and hierarchically structured materials is still in demand for achieving successful tissue regeneration. Here, we combine coaxial electrospinning and 3D printing techniques to prepare bilayered zein-based membranes as a potential dual drug delivery platform for periodontal tissue regeneration. A layer of core-sheath electrospun nanofibers consisting of poly(ethylene oxide) (PEO)/curcumin (Curc)/tetracycline hydrochloride (TH) as the core and zein/poly(ϵ-caprolactone)(PCL)/β-glycerolphosphate (β-GP) as the sheath was deposited over a 3D printed honeycomb PLA/zein/Curc platform in order to render a bilayered structure that can mimic the architecture of periodontal tissue. The physicochemical properties of engineered constructs as well as the release profiles of distinct drugs were mainly controlled by varying the concentration of zein (10, 20, 30%, w/w relative to dry PCL) on the sheath layer of nanofibers, which displayed average diameters ranging from 150 to 400 nm. In vitro experiments demonstrated that the bilayered constructs provided sustained release of distinct drugs over 8 days and exhibited biocompatibility toward human oral keratinocytes (Nok-si) (cell viability >80%) as well as antibacterial activity against distinct bacterial strains including those of the red complex such as Porphyromonas gingivalis and Treponema denticola, which are recognized to elicit aggressive and chronic periodontitis. Our study reveals the potential of zein-based bilayered membranes as a dual drug delivery platform for periodontal tissue regeneration.en
dc.description.affiliationNanotechnology National Laboratory for Agriculture (LNNA) Embrapa Instrumentação, São Paulo
dc.description.affiliationUNESP São Paulo State University School of Pharmaceutical Sciences Department of Clinical Analysis Rodovia Araraquara Jaú, Km 01-s/n-Campos Ville, São Paulo
dc.description.affiliationUNESP São Paulo State University School of Dentistry Department of Dental Materials and Prosthodontics, Rua Humaitá, 1680-Centro, São Paulo
dc.description.affiliationUnespUNESP São Paulo State University School of Pharmaceutical Sciences Department of Clinical Analysis Rodovia Araraquara Jaú, Km 01-s/n-Campos Ville, São Paulo
dc.description.affiliationUnespUNESP São Paulo State University School of Dentistry Department of Dental Materials and Prosthodontics, Rua Humaitá, 1680-Centro, São Paulo
dc.format.extent146-159
dc.identifierhttp://dx.doi.org/10.1021/acsabm.1c01019
dc.identifier.citationACS Applied Bio Materials, v. 5, n. 1, p. 146-159, 2022.
dc.identifier.doi10.1021/acsabm.1c01019
dc.identifier.issn2576-6422
dc.identifier.scopus2-s2.0-85121713020
dc.identifier.urihttp://hdl.handle.net/11449/230113
dc.language.isoeng
dc.relation.ispartofACS Applied Bio Materials
dc.sourceScopus
dc.subjectasymmetric membrane
dc.subjectcontrolled release
dc.subjectcore-shell nanofibers
dc.subjectelectrospinning
dc.subjecthierarchical materials
dc.subjectperiodontal membrane
dc.titleCombining Coaxial Electrospinning and 3D Printing: Design of Biodegradable Bilayered Membranes with Dual Drug Delivery Capability for Periodontitis Treatmenten
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
unesp.author.orcid0000-0002-3884-3236[1]
unesp.author.orcid0000-0002-5592-0627[6]
unesp.departmentAnálises Clínicas - FCFpt

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