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Efficacy and safety of a new heterologous fibrin biopolymer on socket bone healing after tooth extraction: An experimental pre-clinical study

dc.contributor.authorBighetti, Ana Carolina Cestari
dc.contributor.authorCestari, Tania Mary
dc.contributor.authorPaini, Suelen
dc.contributor.authorPomini, Karina T.
dc.contributor.authorBuchaim, Daniela Vieira
dc.contributor.authorOrtiz, Rafael Carneiro
dc.contributor.authorJúnior, Rui Seabra Ferreira [UNESP]
dc.contributor.authorBarraviera, Benedito [UNESP]
dc.contributor.authorBullen, Izabel R. F. R.
dc.contributor.authorGarlet, Gustavo Pompermaier
dc.contributor.authorBuchaim, Rogério Leone
dc.contributor.authorde Assis, Gerson F.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversity of Marilia (UNIMAR)
dc.contributor.institutionUniversity Center of Adamantina (UNI-FAI)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T19:34:11Z
dc.date.issued2024-08-01
dc.description.abstractAim: To assess the efficacy of heterologous fibrin biopolymer (HFB) in promoting alveolar bone healing after tooth extraction in rats. Materials and Methods: The upper right incisors of 48 Wistar rats were extracted. Toothless sockets were filled with HFB (HFBG, n = 24) or blood clot (BCG, n = 24). The tooth extraction sites were subjected to micro-computed tomography (micro-CT), histological, histomorphometric and immunohistochemical (for Runt-related transcription factor 2/Runx2 and tartrate-resistant acid phosphatase/TRAP) analyses on days 0, 7, 14 and 42 after extraction. Results: Socket volume remained similar between days 0 and 14 (69 ± 5.4 mm3), except in the BCG on day 14, when it was 10% lower (p =.043). Although the number of Runx2+ osteoblasts was high and similar in both groups (34 × 102 cells/mm2), the HFBG showed lower inflammatory process and osteoclast activity than BCG at 7 days. On day 14, the number of Runx2+ osteoblasts remained high and similar to the previous period in both groups. However, osteoclast activity increased. This increase was 55% lower in the HFBG than BCG. In the BCG, the presence of an inflammatory process and larger and numerous osteoclasts on day 14 led to resorption of the alveolar bone ridge and newly formed bone. On day 42, numbers of Runx2+ osteoblast and TRAP+ osteoclasts decreased dramatically in both groups. Although the BCG exhibited a more mature cortical bone formation, it exhibited a higher socket reduction (28.3 ± 6.67%) and smaller bone volume (37 ± 5.8 mm3) compared with HFBG (socket reduction of 14.8 ± 7.14% and total bone volume of 46 ± 5.4 mm3). Conclusions: HFB effectively suppresses osteoclast activity and reduces alveolar bone resorption compared with blood clot, thus preventing three-dimensional bone loss, particularly during the early healing period. HFB emerges as a promising biopharmaceutical material for enhancing healing processes after tooth extraction.en
dc.description.affiliationDepartment of Biological Sciences Bauru School of Dentristy University of São Paulo, São Paulo
dc.description.affiliationPostgraduate Program in Structural and Functional Interactions in Rehabilitation University of Marilia (UNIMAR)
dc.description.affiliationTeaching and Research Coordination of the Medical School University Center of Adamantina (UNI-FAI)
dc.description.affiliationCenter for the Study of Venoms and Venomous Animals (CEVAP) São Paulo State University (Univ Estadual Paulista UNESP), São Paulo
dc.description.affiliationGraduate Program in Tropical Diseases Botucatu Medical School (FMB) São Paulo State University (UNESP–Univ Estadual Paulista), São Paulo
dc.description.affiliationGraduate Program in Anatomy of Domestic and Wild Animals Faculty of Veterinary Medicine and Animal Science University of São Paulo (FMVZ/USP)
dc.description.affiliationUnespCenter for the Study of Venoms and Venomous Animals (CEVAP) São Paulo State University (Univ Estadual Paulista UNESP), São Paulo
dc.description.affiliationUnespGraduate Program in Tropical Diseases Botucatu Medical School (FMB) São Paulo State University (UNESP–Univ Estadual Paulista), São Paulo
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipIdCAPES: 001
dc.description.sponsorshipIdCNPq: 303224/2018-5
dc.description.sponsorshipIdCNPq: 306339/2020-0
dc.format.extent1017-1033
dc.identifierhttp://dx.doi.org/10.1111/jcpe.13992
dc.identifier.citationJournal of Clinical Periodontology, v. 51, n. 8, p. 1017-1033, 2024.
dc.identifier.doi10.1111/jcpe.13992
dc.identifier.issn1600-051X
dc.identifier.issn0303-6979
dc.identifier.scopus2-s2.0-85192103484
dc.identifier.urihttps://hdl.handle.net/11449/304198
dc.language.isoeng
dc.relation.ispartofJournal of Clinical Periodontology
dc.sourceScopus
dc.subjectalveolar ridge preservation
dc.subjectbone repair
dc.subjectfibrin tissue adhesive
dc.subjectmicro-computed tomography
dc.subjecttooth extraction
dc.titleEfficacy and safety of a new heterologous fibrin biopolymer on socket bone healing after tooth extraction: An experimental pre-clinical studyen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationa3cdb24b-db92-40d9-b3af-2eacecf9f2ba
relation.isOrgUnitOfPublication.latestForDiscoverya3cdb24b-db92-40d9-b3af-2eacecf9f2ba
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unesp.author.orcid0000-0003-1287-5974[2]
unesp.author.orcid0000-0001-8528-3756[3]
unesp.author.orcid0000-0003-2858-4717[4]
unesp.author.orcid0000-0002-9914-1262[5]
unesp.author.orcid0000-0002-2794-0460[6]
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unesp.author.orcid0000-0002-9855-5594[8]
unesp.author.orcid0000-0002-5069-9433[9]
unesp.author.orcid0000-0002-5071-8382[10]
unesp.author.orcid0000-0002-5881-2218[11]
unesp.author.orcid0000-0001-8225-3164[12]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Centro de Estudos de Venenos e Animais Peçonhentos, Botucatupt

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