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Bone Regeneration Assessment of Polycaprolactone Membrane on Critical-Size Defects in Rat Calvaria
Biomaterials for use in guided bone regeneration (GBR) are constantly being investigated and developed to improve clinical outcomes. The present study aimed to comparatively evaluate the biological performance of different membranes during the bone healing process of 8 mm critical defects in rat cal...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916152/ https://www.ncbi.nlm.nih.gov/pubmed/33572318 http://dx.doi.org/10.3390/membranes11020124 |
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author | Bassi, Ana Paula Farnezi Bizelli, Vinícius Ferreira Francatti, Tamires Mello Rezende de Moares Ferreira, Ana Carulina Carvalho Pereira, Járede Al-Sharani, Hesham Mohammed de Almeida Lucas, Flavia Faverani, Leonardo Perez |
author_facet | Bassi, Ana Paula Farnezi Bizelli, Vinícius Ferreira Francatti, Tamires Mello Rezende de Moares Ferreira, Ana Carulina Carvalho Pereira, Járede Al-Sharani, Hesham Mohammed de Almeida Lucas, Flavia Faverani, Leonardo Perez |
author_sort | Bassi, Ana Paula Farnezi |
collection | PubMed |
description | Biomaterials for use in guided bone regeneration (GBR) are constantly being investigated and developed to improve clinical outcomes. The present study aimed to comparatively evaluate the biological performance of different membranes during the bone healing process of 8 mm critical defects in rat calvaria in order to assess their influence on the quality of the newly formed bone. Seventy-two adult male rats were divided into three experimental groups (n = 24) based on the membranes used: the CG—membrane-free control group (only blood clot, negative control), BG—porcine collagen membrane group (Bio-Guide(®), positive control), and the PCL—polycaprolactone (enriched with 5% hydroxyapatite) membrane group (experimental group). Histological and histometric analyses were performed at 7, 15, 30, and 60 days postoperatively. The quantitative data were analyzed by two-way ANOVA and Tukey’s test (p < 0.05). At 7 and 15 days, the inflammatory responses in the BG and PCL groups were significantly different (p < 0.05). The PCL group, at 15 days, showed a large area of newly formed bone. At 30 and 60 days postoperatively, the PCL and BG groups exhibited similar bone healing, including some specimens showing complete closure of the critical defect (p = 0.799). Thus, the PCL membrane was biocompatible, and has the potential to help with GBR procedures. |
format | Online Article Text |
id | pubmed-7916152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79161522021-03-01 Bone Regeneration Assessment of Polycaprolactone Membrane on Critical-Size Defects in Rat Calvaria Bassi, Ana Paula Farnezi Bizelli, Vinícius Ferreira Francatti, Tamires Mello Rezende de Moares Ferreira, Ana Carulina Carvalho Pereira, Járede Al-Sharani, Hesham Mohammed de Almeida Lucas, Flavia Faverani, Leonardo Perez Membranes (Basel) Article Biomaterials for use in guided bone regeneration (GBR) are constantly being investigated and developed to improve clinical outcomes. The present study aimed to comparatively evaluate the biological performance of different membranes during the bone healing process of 8 mm critical defects in rat calvaria in order to assess their influence on the quality of the newly formed bone. Seventy-two adult male rats were divided into three experimental groups (n = 24) based on the membranes used: the CG—membrane-free control group (only blood clot, negative control), BG—porcine collagen membrane group (Bio-Guide(®), positive control), and the PCL—polycaprolactone (enriched with 5% hydroxyapatite) membrane group (experimental group). Histological and histometric analyses were performed at 7, 15, 30, and 60 days postoperatively. The quantitative data were analyzed by two-way ANOVA and Tukey’s test (p < 0.05). At 7 and 15 days, the inflammatory responses in the BG and PCL groups were significantly different (p < 0.05). The PCL group, at 15 days, showed a large area of newly formed bone. At 30 and 60 days postoperatively, the PCL and BG groups exhibited similar bone healing, including some specimens showing complete closure of the critical defect (p = 0.799). Thus, the PCL membrane was biocompatible, and has the potential to help with GBR procedures. MDPI 2021-02-09 /pmc/articles/PMC7916152/ /pubmed/33572318 http://dx.doi.org/10.3390/membranes11020124 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Bassi, Ana Paula Farnezi Bizelli, Vinícius Ferreira Francatti, Tamires Mello Rezende de Moares Ferreira, Ana Carulina Carvalho Pereira, Járede Al-Sharani, Hesham Mohammed de Almeida Lucas, Flavia Faverani, Leonardo Perez Bone Regeneration Assessment of Polycaprolactone Membrane on Critical-Size Defects in Rat Calvaria |
title | Bone Regeneration Assessment of Polycaprolactone Membrane on Critical-Size Defects in Rat Calvaria |
title_full | Bone Regeneration Assessment of Polycaprolactone Membrane on Critical-Size Defects in Rat Calvaria |
title_fullStr | Bone Regeneration Assessment of Polycaprolactone Membrane on Critical-Size Defects in Rat Calvaria |
title_full_unstemmed | Bone Regeneration Assessment of Polycaprolactone Membrane on Critical-Size Defects in Rat Calvaria |
title_short | Bone Regeneration Assessment of Polycaprolactone Membrane on Critical-Size Defects in Rat Calvaria |
title_sort | bone regeneration assessment of polycaprolactone membrane on critical-size defects in rat calvaria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916152/ https://www.ncbi.nlm.nih.gov/pubmed/33572318 http://dx.doi.org/10.3390/membranes11020124 |
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