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Biocompatibility of a HA/β-TCP/C Scaffold as a Pulp-Capping Agent for Vital Pulp Treatment: An In Vivo Study in Rat Molars
Bioceramic materials possess desirable biological properties, highlighting their non-reactivity and osteoconductivity. Their use has been extended in vital pulp treatment. The purpose of this study was to evaluate and compare the effects of beta-tricalcium phosphate (β-TCP), hydroxyapatite (HA), and...
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/PMC8068992/ https://www.ncbi.nlm.nih.gov/pubmed/33918101 http://dx.doi.org/10.3390/ijerph18083936 |
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author | Guerrero-Gironés, Julia Alcaina-Lorente, Antonia Ortiz-Ruiz, Clara Ortiz-Ruiz, Eduardo Pecci-Lloret, María P. Ortiz-Ruiz, Antonio José Rodríguez-Lozano, Francisco Javier Pecci-Lloret, Miguel R. |
author_facet | Guerrero-Gironés, Julia Alcaina-Lorente, Antonia Ortiz-Ruiz, Clara Ortiz-Ruiz, Eduardo Pecci-Lloret, María P. Ortiz-Ruiz, Antonio José Rodríguez-Lozano, Francisco Javier Pecci-Lloret, Miguel R. |
author_sort | Guerrero-Gironés, Julia |
collection | PubMed |
description | Bioceramic materials possess desirable biological properties, highlighting their non-reactivity and osteoconductivity. Their use has been extended in vital pulp treatment. The purpose of this study was to evaluate and compare the effects of beta-tricalcium phosphate (β-TCP), hydroxyapatite (HA), and collagen (C) scaffold with mineral trioxide aggregate (MTA) on the vital pulp of rat molars. Thirty-two molars of Sprague–Dawley rats underwent direct pulp capping with β-TCP/HA/C (n = 16) and MTA (n = 16). After 30 days, the following parameters were evaluated in the tested samples: the degree of pulp inflammation and pulp vitality, the presence of reparative dentin, the homogeneity of the odontoblastic layer, and the presence of pulp fibrosis. No statistically significant differences were observed between HA/β-TCP/C and MTA in terms of the degree of inflammation (p = 0.124). Significant differences were found in reparative dentin formation between the treatment groups (p = 0.0005). Dentin bridge formation was observed in the MTA-treated group. The local action of HA/β-TCP/C is similar to that of MTA when used as an agent for pulp vital treatment in terms of absence of inflammation and maintenance of pulp vitality, although there are significant differences between both materials regarding the formation of dentin bridges. |
format | Online Article Text |
id | pubmed-8068992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80689922021-04-26 Biocompatibility of a HA/β-TCP/C Scaffold as a Pulp-Capping Agent for Vital Pulp Treatment: An In Vivo Study in Rat Molars Guerrero-Gironés, Julia Alcaina-Lorente, Antonia Ortiz-Ruiz, Clara Ortiz-Ruiz, Eduardo Pecci-Lloret, María P. Ortiz-Ruiz, Antonio José Rodríguez-Lozano, Francisco Javier Pecci-Lloret, Miguel R. Int J Environ Res Public Health Article Bioceramic materials possess desirable biological properties, highlighting their non-reactivity and osteoconductivity. Their use has been extended in vital pulp treatment. The purpose of this study was to evaluate and compare the effects of beta-tricalcium phosphate (β-TCP), hydroxyapatite (HA), and collagen (C) scaffold with mineral trioxide aggregate (MTA) on the vital pulp of rat molars. Thirty-two molars of Sprague–Dawley rats underwent direct pulp capping with β-TCP/HA/C (n = 16) and MTA (n = 16). After 30 days, the following parameters were evaluated in the tested samples: the degree of pulp inflammation and pulp vitality, the presence of reparative dentin, the homogeneity of the odontoblastic layer, and the presence of pulp fibrosis. No statistically significant differences were observed between HA/β-TCP/C and MTA in terms of the degree of inflammation (p = 0.124). Significant differences were found in reparative dentin formation between the treatment groups (p = 0.0005). Dentin bridge formation was observed in the MTA-treated group. The local action of HA/β-TCP/C is similar to that of MTA when used as an agent for pulp vital treatment in terms of absence of inflammation and maintenance of pulp vitality, although there are significant differences between both materials regarding the formation of dentin bridges. MDPI 2021-04-08 /pmc/articles/PMC8068992/ /pubmed/33918101 http://dx.doi.org/10.3390/ijerph18083936 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 Guerrero-Gironés, Julia Alcaina-Lorente, Antonia Ortiz-Ruiz, Clara Ortiz-Ruiz, Eduardo Pecci-Lloret, María P. Ortiz-Ruiz, Antonio José Rodríguez-Lozano, Francisco Javier Pecci-Lloret, Miguel R. Biocompatibility of a HA/β-TCP/C Scaffold as a Pulp-Capping Agent for Vital Pulp Treatment: An In Vivo Study in Rat Molars |
title | Biocompatibility of a HA/β-TCP/C Scaffold as a Pulp-Capping Agent for Vital Pulp Treatment: An In Vivo Study in Rat Molars |
title_full | Biocompatibility of a HA/β-TCP/C Scaffold as a Pulp-Capping Agent for Vital Pulp Treatment: An In Vivo Study in Rat Molars |
title_fullStr | Biocompatibility of a HA/β-TCP/C Scaffold as a Pulp-Capping Agent for Vital Pulp Treatment: An In Vivo Study in Rat Molars |
title_full_unstemmed | Biocompatibility of a HA/β-TCP/C Scaffold as a Pulp-Capping Agent for Vital Pulp Treatment: An In Vivo Study in Rat Molars |
title_short | Biocompatibility of a HA/β-TCP/C Scaffold as a Pulp-Capping Agent for Vital Pulp Treatment: An In Vivo Study in Rat Molars |
title_sort | biocompatibility of a ha/β-tcp/c scaffold as a pulp-capping agent for vital pulp treatment: an in vivo study in rat molars |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8068992/ https://www.ncbi.nlm.nih.gov/pubmed/33918101 http://dx.doi.org/10.3390/ijerph18083936 |
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