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Polydioxanone Enhances Bone Regeneration After Resection and Reconstruction of Rat Femur with rhBMP2.
Rios, Barbara Ribeiro; Barbosa, Stéfany; da Silva, William Phillip Pereira; Quirino Louzada, Mario Jefferson; Ervolino, Edilson; Kalil, Eduardo C; Shibli, Jamil Awad; Faverani, Leonardo P.
Afiliação
  • Rios BR; Division of Oral and Maxillofacial Surgery and Implantology, Department of Diagnosis and Surgery, School of Dentistry, São Paulo State University (UNESP), Araçatuba, São Paulo, Brazil.
  • Barbosa S; Division of Oral and Maxillofacial Surgery and Implantology, Department of Diagnosis and Surgery, School of Dentistry, São Paulo State University (UNESP), Araçatuba, São Paulo, Brazil.
  • da Silva WPP; Division of Oral and Maxillofacial Surgery and Implantology, Department of Diagnosis and Surgery, School of Dentistry, São Paulo State University (UNESP), Araçatuba, São Paulo, Brazil.
  • Quirino Louzada MJ; Catholic Salesian Auxilium University Center, Faculty of Dentistry, Araçatuba, São Paulo, Brazil.
  • Ervolino E; Division of Histology, Department of Basic Sciences, School of Dentistry, São Paulo State University (UNESP), Araçatuba, São Paulo, Brazil.
  • Kalil EC; Dental Research Division, Department of Periodontology, Guarulhos University, Centro, Guarulhos, Brazil.
  • Shibli JA; Dental Research Division, Department of Periodontology, Guarulhos University, Centro, Guarulhos, Brazil.
  • Faverani LP; Division of Oral and Maxillofacial Surgery and Implantology, Department of Diagnosis and Surgery, School of Dentistry, São Paulo State University (UNESP), Araçatuba, São Paulo, Brazil.
Tissue Eng Part C Methods ; 30(3): 102-112, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38271574
ABSTRACT
The aim of this study was to assess the bone regeneration potential of a polydioxanone (PDO) scaffold together with recombinant human bone morphogenetic protein-2 (rhBMP-2) for the reconstruction of large bone defect. In total, 24 male rats (6 months old) were subjected to bilateral femoral stabilization using titanium plates to create a 2 mm gap, and reconstruction using rhBMP-2 (Infuse®; 3.25 µg). The bone defects were covered with PDO (PDO group), or with titanium mesh (Ti group). Animals were euthanized on days 14 and 60. Simultaneously, 16 rats received PDO and Ti in their dorsum for the purpose of biocompatibility analysis at 3, 5, 7, and 10 days postoperatively. X-ray densitometry showed a higher density in the PDO group on day 14. On day 60, coverage of the bone defect with PDO showed a larger quantity of newly formed bone than that found for the Ti group, a lower inflammatory infiltrate value, and a more significant number of blood vessels on day 14. By immunohistochemical assessment, runt-related transcription factor 2 (RUNX2) and osteocalcin (OCN) showed higher labeling on day 14 in the PDO group. On day 60, bone morphogenetic protein-2 (BMP-2) showed higher labeling in the PDO group, whereas Ti showed higher labeling for osteoprotegerin, nuclear factor kappa B ligand-activating receptor, RUNX2, and OCN. Furthermore, biocompatibility analysis showed a higher inflammatory response in the Ti group. The PDO scaffold enhanced bone regeneration when associated with rhBMP-2 in rat femur reconstruction. Impact statement Regeneration of segmental bone defects is a difficult task, and several techniques and materials have been used. Recent advances in the production of synthetic polymers, such as polydioxanone (PDO), produced by three-dimensional printing, have shown distinct characteristics that could improve tissue regeneration even in an important bone defect. The present preclinical study showed that PDO membranes used as scaffolds to carry recombinant human bone morphogenetic protein-2 (rhBMP-2) improved bone tissue regeneration by more than 8-fold when compared with titanium mesh, suggesting that PDO membranes could be a feasible and useful material for use in guided bone regeneration. (In English, viable is only used for living creatures capable of sustaining life.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polidioxanona / Subunidade alfa 1 de Fator de Ligação ao Core Limite: Animals / Humans / Infant / Male Idioma: En Revista: Tissue Eng Part C Methods Assunto da revista: BIOTECNOLOGIA / HISTOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polidioxanona / Subunidade alfa 1 de Fator de Ligação ao Core Limite: Animals / Humans / Infant / Male Idioma: En Revista: Tissue Eng Part C Methods Assunto da revista: BIOTECNOLOGIA / HISTOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Estados Unidos