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Chitosan (CS)/Hydroxyapatite (HA)/Tricalcium Phosphate (β-TCP)-Based Composites as a Potential Material for Pulp Tissue Regeneration

This research focused on developing new materials for endodontic treatments to restore tissues affected by infectious or inflammatory processes. Three materials were studied, namely tricalcium phosphate β-hydroxyapatite (β-TCP), commercial and natural hydroxyapatite (HA), and chitosan (CS), in diffe...

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Autores principales: Zamora, Ingrid, Alfonso Morales, Gilbert, Castro, Jorge Iván, Ruiz Rojas, Lina Marcela, Valencia-Llano, Carlos Humberto, Mina Hernandez, Jose Herminsul, Valencia Zapata, Mayra Eliana, Grande-Tovar, Carlos David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10421191/
https://www.ncbi.nlm.nih.gov/pubmed/37571109
http://dx.doi.org/10.3390/polym15153213
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author Zamora, Ingrid
Alfonso Morales, Gilbert
Castro, Jorge Iván
Ruiz Rojas, Lina Marcela
Valencia-Llano, Carlos Humberto
Mina Hernandez, Jose Herminsul
Valencia Zapata, Mayra Eliana
Grande-Tovar, Carlos David
author_facet Zamora, Ingrid
Alfonso Morales, Gilbert
Castro, Jorge Iván
Ruiz Rojas, Lina Marcela
Valencia-Llano, Carlos Humberto
Mina Hernandez, Jose Herminsul
Valencia Zapata, Mayra Eliana
Grande-Tovar, Carlos David
author_sort Zamora, Ingrid
collection PubMed
description This research focused on developing new materials for endodontic treatments to restore tissues affected by infectious or inflammatory processes. Three materials were studied, namely tricalcium phosphate β-hydroxyapatite (β-TCP), commercial and natural hydroxyapatite (HA), and chitosan (CS), in different proportions. The chemical characterization using infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analysis confirmed the composition of the composite. Scanning electron microscopy (SEM) demonstrated that the design and origin of the HA, whether natural or commercial, did not affect the morphology of the composites. In vitro studies using Artemia salina (A. salina) indicated that all three experimental materials were biocompatible after 24 h, with no significant differences in mortality rate observed among the groups. The subdermal implantation of the materials in block form exhibited biocompatibility and biodegradability after 30 and 60 days, with the larger particles undergoing fragmentation and connective tissue formation consisting of collagen type III fibers, blood vessels, and inflammatory cells. The implanted material continued to undergo resorption during this process. The results obtained in this research contribute to developing endodontic technologies for tissue recovery and regeneration.
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spelling pubmed-104211912023-08-12 Chitosan (CS)/Hydroxyapatite (HA)/Tricalcium Phosphate (β-TCP)-Based Composites as a Potential Material for Pulp Tissue Regeneration Zamora, Ingrid Alfonso Morales, Gilbert Castro, Jorge Iván Ruiz Rojas, Lina Marcela Valencia-Llano, Carlos Humberto Mina Hernandez, Jose Herminsul Valencia Zapata, Mayra Eliana Grande-Tovar, Carlos David Polymers (Basel) Article This research focused on developing new materials for endodontic treatments to restore tissues affected by infectious or inflammatory processes. Three materials were studied, namely tricalcium phosphate β-hydroxyapatite (β-TCP), commercial and natural hydroxyapatite (HA), and chitosan (CS), in different proportions. The chemical characterization using infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analysis confirmed the composition of the composite. Scanning electron microscopy (SEM) demonstrated that the design and origin of the HA, whether natural or commercial, did not affect the morphology of the composites. In vitro studies using Artemia salina (A. salina) indicated that all three experimental materials were biocompatible after 24 h, with no significant differences in mortality rate observed among the groups. The subdermal implantation of the materials in block form exhibited biocompatibility and biodegradability after 30 and 60 days, with the larger particles undergoing fragmentation and connective tissue formation consisting of collagen type III fibers, blood vessels, and inflammatory cells. The implanted material continued to undergo resorption during this process. The results obtained in this research contribute to developing endodontic technologies for tissue recovery and regeneration. MDPI 2023-07-28 /pmc/articles/PMC10421191/ /pubmed/37571109 http://dx.doi.org/10.3390/polym15153213 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
Zamora, Ingrid
Alfonso Morales, Gilbert
Castro, Jorge Iván
Ruiz Rojas, Lina Marcela
Valencia-Llano, Carlos Humberto
Mina Hernandez, Jose Herminsul
Valencia Zapata, Mayra Eliana
Grande-Tovar, Carlos David
Chitosan (CS)/Hydroxyapatite (HA)/Tricalcium Phosphate (β-TCP)-Based Composites as a Potential Material for Pulp Tissue Regeneration
title Chitosan (CS)/Hydroxyapatite (HA)/Tricalcium Phosphate (β-TCP)-Based Composites as a Potential Material for Pulp Tissue Regeneration
title_full Chitosan (CS)/Hydroxyapatite (HA)/Tricalcium Phosphate (β-TCP)-Based Composites as a Potential Material for Pulp Tissue Regeneration
title_fullStr Chitosan (CS)/Hydroxyapatite (HA)/Tricalcium Phosphate (β-TCP)-Based Composites as a Potential Material for Pulp Tissue Regeneration
title_full_unstemmed Chitosan (CS)/Hydroxyapatite (HA)/Tricalcium Phosphate (β-TCP)-Based Composites as a Potential Material for Pulp Tissue Regeneration
title_short Chitosan (CS)/Hydroxyapatite (HA)/Tricalcium Phosphate (β-TCP)-Based Composites as a Potential Material for Pulp Tissue Regeneration
title_sort chitosan (cs)/hydroxyapatite (ha)/tricalcium phosphate (β-tcp)-based composites as a potential material for pulp tissue regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10421191/
https://www.ncbi.nlm.nih.gov/pubmed/37571109
http://dx.doi.org/10.3390/polym15153213
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