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In Vivo Investigation of Polymer-Ceramic PCL/HA and PCL/β-TCP 3D Composite Scaffolds and Electrical Stimulation for Bone Regeneration

Critical bone defects are a major clinical challenge in reconstructive bone surgery. Polycaprolactone (PCL) mixed with bioceramics, such as hydroxyapatite (HA) and tricalcium phosphate (TCP), create composite scaffolds with improved biological recognition and bioactivity. Electrical stimulation (ES)...

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Autores principales: Helaehil, Júlia Venturini, Lourenço, Carina Basqueira, Huang, Boyang, Helaehil, Luiza Venturini, de Camargo, Isaque Xavier, Chiarotto, Gabriela Bortolança, Santamaria-Jr, Milton, Bártolo, Paulo, Caetano, Guilherme Ferreira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8747620/
https://www.ncbi.nlm.nih.gov/pubmed/35012090
http://dx.doi.org/10.3390/polym14010065
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author Helaehil, Júlia Venturini
Lourenço, Carina Basqueira
Huang, Boyang
Helaehil, Luiza Venturini
de Camargo, Isaque Xavier
Chiarotto, Gabriela Bortolança
Santamaria-Jr, Milton
Bártolo, Paulo
Caetano, Guilherme Ferreira
author_facet Helaehil, Júlia Venturini
Lourenço, Carina Basqueira
Huang, Boyang
Helaehil, Luiza Venturini
de Camargo, Isaque Xavier
Chiarotto, Gabriela Bortolança
Santamaria-Jr, Milton
Bártolo, Paulo
Caetano, Guilherme Ferreira
author_sort Helaehil, Júlia Venturini
collection PubMed
description Critical bone defects are a major clinical challenge in reconstructive bone surgery. Polycaprolactone (PCL) mixed with bioceramics, such as hydroxyapatite (HA) and tricalcium phosphate (TCP), create composite scaffolds with improved biological recognition and bioactivity. Electrical stimulation (ES) aims to compensate the compromised endogenous electrical signals and to stimulate cell proliferation and differentiation. We investigated the effects of composite scaffolds (PCL with HA; and PCL with β-TCP) and the use of ES on critical bone defects in Wistar rats using eight experimental groups: untreated, ES, PCL, PCL/ES, HA, HA/ES, TCP, and TCP/ES. The investigation was based on histomorphometry, immunohistochemistry, and gene expression analysis. The vascular area was greater in the HA/ES group on days 30 and 60. Tissue mineralization was greater in the HA, HA/ES, and TCP groups at day 30, and TCP/ES at day 60. Bmp-2 gene expression was higher in the HA, TCP, and TCP/ES groups at day 30, and in the TCP/ES and PCL/ES groups at day 60. Runx-2, Osterix, and Osteopontin gene expression were also higher in the TCP/ES group at day 60. These results suggest that scaffolds printed with PCL and TCP, when paired with electrical therapy application, improve bone regeneration.
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spelling pubmed-87476202022-01-11 In Vivo Investigation of Polymer-Ceramic PCL/HA and PCL/β-TCP 3D Composite Scaffolds and Electrical Stimulation for Bone Regeneration Helaehil, Júlia Venturini Lourenço, Carina Basqueira Huang, Boyang Helaehil, Luiza Venturini de Camargo, Isaque Xavier Chiarotto, Gabriela Bortolança Santamaria-Jr, Milton Bártolo, Paulo Caetano, Guilherme Ferreira Polymers (Basel) Article Critical bone defects are a major clinical challenge in reconstructive bone surgery. Polycaprolactone (PCL) mixed with bioceramics, such as hydroxyapatite (HA) and tricalcium phosphate (TCP), create composite scaffolds with improved biological recognition and bioactivity. Electrical stimulation (ES) aims to compensate the compromised endogenous electrical signals and to stimulate cell proliferation and differentiation. We investigated the effects of composite scaffolds (PCL with HA; and PCL with β-TCP) and the use of ES on critical bone defects in Wistar rats using eight experimental groups: untreated, ES, PCL, PCL/ES, HA, HA/ES, TCP, and TCP/ES. The investigation was based on histomorphometry, immunohistochemistry, and gene expression analysis. The vascular area was greater in the HA/ES group on days 30 and 60. Tissue mineralization was greater in the HA, HA/ES, and TCP groups at day 30, and TCP/ES at day 60. Bmp-2 gene expression was higher in the HA, TCP, and TCP/ES groups at day 30, and in the TCP/ES and PCL/ES groups at day 60. Runx-2, Osterix, and Osteopontin gene expression were also higher in the TCP/ES group at day 60. These results suggest that scaffolds printed with PCL and TCP, when paired with electrical therapy application, improve bone regeneration. MDPI 2021-12-25 /pmc/articles/PMC8747620/ /pubmed/35012090 http://dx.doi.org/10.3390/polym14010065 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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Helaehil, Júlia Venturini
Lourenço, Carina Basqueira
Huang, Boyang
Helaehil, Luiza Venturini
de Camargo, Isaque Xavier
Chiarotto, Gabriela Bortolança
Santamaria-Jr, Milton
Bártolo, Paulo
Caetano, Guilherme Ferreira
In Vivo Investigation of Polymer-Ceramic PCL/HA and PCL/β-TCP 3D Composite Scaffolds and Electrical Stimulation for Bone Regeneration
title In Vivo Investigation of Polymer-Ceramic PCL/HA and PCL/β-TCP 3D Composite Scaffolds and Electrical Stimulation for Bone Regeneration
title_full In Vivo Investigation of Polymer-Ceramic PCL/HA and PCL/β-TCP 3D Composite Scaffolds and Electrical Stimulation for Bone Regeneration
title_fullStr In Vivo Investigation of Polymer-Ceramic PCL/HA and PCL/β-TCP 3D Composite Scaffolds and Electrical Stimulation for Bone Regeneration
title_full_unstemmed In Vivo Investigation of Polymer-Ceramic PCL/HA and PCL/β-TCP 3D Composite Scaffolds and Electrical Stimulation for Bone Regeneration
title_short In Vivo Investigation of Polymer-Ceramic PCL/HA and PCL/β-TCP 3D Composite Scaffolds and Electrical Stimulation for Bone Regeneration
title_sort in vivo investigation of polymer-ceramic pcl/ha and pcl/β-tcp 3d composite scaffolds and electrical stimulation for bone regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8747620/
https://www.ncbi.nlm.nih.gov/pubmed/35012090
http://dx.doi.org/10.3390/polym14010065
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