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Smart Delivery of Biomolecules Interfering with Peri-Implant Repair in Osteoporotic Rats

dc.contributor.authorPaludetto, Laura Vidoto [UNESP]
dc.contributor.authorMonteiro, Naara Gabriela [UNESP]
dc.contributor.authorBreseghello, Isadora [UNESP]
dc.contributor.authorde Souza Batista, Fábio Roberto [UNESP]
dc.contributor.authorAntoniali, Cristina [UNESP]
dc.contributor.authorLisboa-Filho, Paulo Noronha [UNESP]
dc.contributor.authorOkamoto, Roberta [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T19:30:16Z
dc.date.issued2024-08-01
dc.description.abstractBisphosphonates are widely used for the treatment of postmenopausal osteoporosis; however, they cause several long-term side effects, necessitating the investigation of local ways to improve osseointegration in compromised bone tissue. The purpose of this study was to evaluate peri-implant bone repair using implants functionalized with zoledronic acid alone (OVX ZOL group, n = 11), zoledronic acid + teriparatide (OVX ZOL + TERI group, n = 11), and zoledronic acid + ruterpy (OVX ZOL + TERPY group, n = 11) compared to the control group (OVX CONV, n = 11). Analyses included computer-assisted microtomography, qualitative histologic analysis, and real-time PCR analysis. Histologically, all functionalized surfaces improved peri-implant repair, with the OVX ZOL + TERI group standing out. Similar results were found in computerized microtomography analysis. In real-time PCR analysis, however, the OVX ZOL and OVX ZOL + TERPY groups showed better results for bone formation, with the OVX ZOL + TERPY group standing out, while there were no statistical differences between the OVX CONV and OVX ZOL + TERI groups for the genes studied at 28 postoperative days. Nevertheless, all functionalized groups showed a reduced rate of bone resorption. In short, all surface functionalization groups outperformed the control group, with overall better results for the OVX ZOL + TERI group.en
dc.description.affiliationDepartment of Basic Sciences Araçatuba Dental School São Paulo State University Júlio de Mesquita Filho—UNESP, SP
dc.description.affiliationDepartment of Physics and Meteorology Bauru Sciences School São Paulo State University Júlio de Mesquita Filho—UNESP, SP
dc.description.affiliationUnespDepartment of Basic Sciences Araçatuba Dental School São Paulo State University Júlio de Mesquita Filho—UNESP, SP
dc.description.affiliationUnespDepartment of Physics and Meteorology Bauru Sciences School São Paulo State University Júlio de Mesquita Filho—UNESP, SP
dc.identifierhttp://dx.doi.org/10.3390/ijms25168963
dc.identifier.citationInternational Journal of Molecular Sciences, v. 25, n. 16, 2024.
dc.identifier.doi10.3390/ijms25168963
dc.identifier.issn1422-0067
dc.identifier.issn1661-6596
dc.identifier.scopus2-s2.0-85202670819
dc.identifier.urihttps://hdl.handle.net/11449/303642
dc.language.isoeng
dc.relation.ispartofInternational Journal of Molecular Sciences
dc.sourceScopus
dc.subjectdental implants
dc.subjectosteoporosis
dc.subjectruterpy
dc.subjectteriparatide
dc.subjectzoledronic acid
dc.titleSmart Delivery of Biomolecules Interfering with Peri-Implant Repair in Osteoporotic Ratsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.author.orcid0000-0001-6251-8604[1]
unesp.author.orcid0000-0002-2857-9195[2]
unesp.author.orcid0000-0002-0315-6161[5]
unesp.author.orcid0000-0002-7734-4069[6]
unesp.author.orcid0000-0002-6773-6966[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt

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