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Publicação:
Bioactive molecule-loaded drug delivery systems to optimize bone tissue repair

dc.contributor.authorOshiro, João Augusto [UNESP]
dc.contributor.authorSato, Mariana Rillo [UNESP]
dc.contributor.authorScardueli, Cassio Rocha [UNESP]
dc.contributor.authorde Oliveira, Guilherme José Pimentel Lopes [UNESP]
dc.contributor.authorAbuçafy, Marina Paiva [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:33:10Z
dc.date.available2018-12-11T17:33:10Z
dc.date.issued2017-08-01
dc.description.abstractBioactive molecules such as peptides and proteins can optimize the repair of bone tissue; however, the results are often unpredictable when administered alone, owing to their short biological half-life and instability. Thus, the development of bioactive molecule-loaded drug delivery systems (DDS) to repair bone tissue has been the subject of intense research. DDS can optimize the repair of bone tissue owing to their physicochemical properties, which improve cellular interactions and enable the incorporation and prolonged release of bioactive molecules. These characteristics are fundamental to favor bone tissue homeostasis, since the biological activity of these factors depends on how accessible they are to the cell. Considering the importance of these DDS, this review aims to present relevant information on DDS when loaded with osteogenic growth peptide and bone morphogenetic protein. These are bioactive molecules that are capable of modulating the differentiation and proliferation of mesenchymal cells in bone tissue cells. Moreover, we will present different approaches using these peptide and protein-loaded DDS, such as synthetic membranes and scaffolds for bone regeneration, synthetic grafts, bone cements, liposomes, and micelles, which aim at improving the therapeutic effectiveness, and we will compare their advantages with commercial systems.en
dc.description.affiliationFaculdade de Ciências Farmacêuticas UNESP-Univ Estadual Paulista, Araraquara-Jaú, Km 1
dc.description.affiliationFaculdade de Odontologia Universidade Estadual Paulista (UNESP), Humaitá, 1680
dc.description.affiliationUnespFaculdade de Ciências Farmacêuticas UNESP-Univ Estadual Paulista, Araraquara-Jaú, Km 1
dc.description.affiliationUnespFaculdade de Odontologia Universidade Estadual Paulista (UNESP), Humaitá, 1680
dc.format.extent850-863
dc.identifierhttp://dx.doi.org/10.2174/1389203718666170328111605
dc.identifier.citationCurrent Protein and Peptide Science, v. 18, n. 8, p. 850-863, 2017.
dc.identifier.doi10.2174/1389203718666170328111605
dc.identifier.issn1875-5550
dc.identifier.issn1389-2037
dc.identifier.lattes1427125996716282
dc.identifier.scopus2-s2.0-85022206438
dc.identifier.urihttp://hdl.handle.net/11449/179018
dc.language.isoeng
dc.relation.ispartofCurrent Protein and Peptide Science
dc.relation.ispartofsjr0,858
dc.rights.accessRightsAcesso restritopt
dc.sourceScopus
dc.subjectBioactive molecules
dc.subjectBone morphogenetic protein
dc.subjectDrug delivery systems
dc.subjectOsteogenic growth peptide
dc.subjectTissue repair
dc.titleBioactive molecule-loaded drug delivery systems to optimize bone tissue repairen
dc.typeResenhapt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
unesp.author.lattes1427125996716282
unesp.departmentFármacos e Medicamentos - FCFpt

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