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Functionalization of a Cortical Membrane with a Photodynamic Protocol

Guided bone regeneration (GBR) comprehends the application of membranes to drive bone healing and to exclude non-osteogenic tissues from interfering with bone regeneration. However, the membranes may be exposed to bacterial attack, with the risk of failure of the GBR. Recently, an antibacterial phot...

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Autores principales: Pierfelice, Tania Vanessa, D’Amico, Emira, D’Ercole, Simonetta, Lepore, Stefania, Piattelli, Adriano, Barone, Antonio, Iezzi, Giovanna, Petrini, Morena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057199/
https://www.ncbi.nlm.nih.gov/pubmed/36976057
http://dx.doi.org/10.3390/jfb14030133
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author Pierfelice, Tania Vanessa
D’Amico, Emira
D’Ercole, Simonetta
Lepore, Stefania
Piattelli, Adriano
Barone, Antonio
Iezzi, Giovanna
Petrini, Morena
author_facet Pierfelice, Tania Vanessa
D’Amico, Emira
D’Ercole, Simonetta
Lepore, Stefania
Piattelli, Adriano
Barone, Antonio
Iezzi, Giovanna
Petrini, Morena
author_sort Pierfelice, Tania Vanessa
collection PubMed
description Guided bone regeneration (GBR) comprehends the application of membranes to drive bone healing and to exclude non-osteogenic tissues from interfering with bone regeneration. However, the membranes may be exposed to bacterial attack, with the risk of failure of the GBR. Recently, an antibacterial photodynamic protocol (ALAD-PDT) based on a gel with 5% 5-aminolevulinic acid incubated for 45 min and irradiated for 7 min by a LED light at 630 nm, also showed a pro-proliferative effect on human fibroblasts and osteoblasts. The present study hypothesized that the functionalization of a porcine cortical membrane (soft-curved lamina, OsteoBiol) with ALAD-PDT might promote its osteoconductive properties. TEST 1 aimed to verify the response of osteoblasts seeded on lamina with respect to the plate surface (CTRL). TEST 2 aimed to investigate the effects of ALAD-PDT on the osteoblasts cultured on the lamina. SEM analyses were performed to study the topographical characteristics of the membrane surface, the adhesion, and the morphology of cells at 3 days. The viability was assessed at 3 days, the ALP activity at 7 days, and calcium deposition at 14 days. Results showed the porous surface of the lamina and the increase in cell attachment of osteoblasts with respect to controls. The proliferation, the ALP, and bone mineralization activity of osteoblasts seeded on lamina resulted in being significantly higher (p < 0.0001) than controls. Results also showed an additional significative enhancement (p < 0.0001) in the proliferative rate in ALP and calcium deposition after applying ALAD-PDT. In conclusion, the functionalization of the cortical membranes cultured with osteoblasts with the ALAD-PDT improved their osteoconductive properties.
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spelling pubmed-100571992023-03-30 Functionalization of a Cortical Membrane with a Photodynamic Protocol Pierfelice, Tania Vanessa D’Amico, Emira D’Ercole, Simonetta Lepore, Stefania Piattelli, Adriano Barone, Antonio Iezzi, Giovanna Petrini, Morena J Funct Biomater Article Guided bone regeneration (GBR) comprehends the application of membranes to drive bone healing and to exclude non-osteogenic tissues from interfering with bone regeneration. However, the membranes may be exposed to bacterial attack, with the risk of failure of the GBR. Recently, an antibacterial photodynamic protocol (ALAD-PDT) based on a gel with 5% 5-aminolevulinic acid incubated for 45 min and irradiated for 7 min by a LED light at 630 nm, also showed a pro-proliferative effect on human fibroblasts and osteoblasts. The present study hypothesized that the functionalization of a porcine cortical membrane (soft-curved lamina, OsteoBiol) with ALAD-PDT might promote its osteoconductive properties. TEST 1 aimed to verify the response of osteoblasts seeded on lamina with respect to the plate surface (CTRL). TEST 2 aimed to investigate the effects of ALAD-PDT on the osteoblasts cultured on the lamina. SEM analyses were performed to study the topographical characteristics of the membrane surface, the adhesion, and the morphology of cells at 3 days. The viability was assessed at 3 days, the ALP activity at 7 days, and calcium deposition at 14 days. Results showed the porous surface of the lamina and the increase in cell attachment of osteoblasts with respect to controls. The proliferation, the ALP, and bone mineralization activity of osteoblasts seeded on lamina resulted in being significantly higher (p < 0.0001) than controls. Results also showed an additional significative enhancement (p < 0.0001) in the proliferative rate in ALP and calcium deposition after applying ALAD-PDT. In conclusion, the functionalization of the cortical membranes cultured with osteoblasts with the ALAD-PDT improved their osteoconductive properties. MDPI 2023-02-27 /pmc/articles/PMC10057199/ /pubmed/36976057 http://dx.doi.org/10.3390/jfb14030133 Text en © 2023 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
Pierfelice, Tania Vanessa
D’Amico, Emira
D’Ercole, Simonetta
Lepore, Stefania
Piattelli, Adriano
Barone, Antonio
Iezzi, Giovanna
Petrini, Morena
Functionalization of a Cortical Membrane with a Photodynamic Protocol
title Functionalization of a Cortical Membrane with a Photodynamic Protocol
title_full Functionalization of a Cortical Membrane with a Photodynamic Protocol
title_fullStr Functionalization of a Cortical Membrane with a Photodynamic Protocol
title_full_unstemmed Functionalization of a Cortical Membrane with a Photodynamic Protocol
title_short Functionalization of a Cortical Membrane with a Photodynamic Protocol
title_sort functionalization of a cortical membrane with a photodynamic protocol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057199/
https://www.ncbi.nlm.nih.gov/pubmed/36976057
http://dx.doi.org/10.3390/jfb14030133
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