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Subcutaneous Connective Tissue Reactions to Various Endodontic Biomaterials: An Animal Study

BACKGROUND AND AIMS: Biocompatibility of root-end filling materials is a matter of debate. The aim of this study was to compare the biocompatibility of a variety of commercial ProRoot WMTA cements and a resin-based cement (Geristore®) with different pH values of setting reaction and different alumin...

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Autores principales: Saghiri, Mohammad Ali, Tanideh, Nader, Garcia-Godoy, Franklin, Lotfi, Mehrdad, Karamifar, Kasra, Amanat, Dariush
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593200/
https://www.ncbi.nlm.nih.gov/pubmed/23486841
http://dx.doi.org/10.5681/joddd.2013.003
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author Saghiri, Mohammad Ali
Tanideh, Nader
Garcia-Godoy, Franklin
Lotfi, Mehrdad
Karamifar, Kasra
Amanat, Dariush
author_facet Saghiri, Mohammad Ali
Tanideh, Nader
Garcia-Godoy, Franklin
Lotfi, Mehrdad
Karamifar, Kasra
Amanat, Dariush
author_sort Saghiri, Mohammad Ali
collection PubMed
description BACKGROUND AND AIMS: Biocompatibility of root-end filling materials is a matter of debate. The aim of this study was to compare the biocompatibility of a variety of commercial ProRoot WMTA cements and a resin-based cement (Geristore®) with different pH values of setting reaction and different aluminum contents, implanted into the subcutaneous connective tissue of rats at various time intervals. MATERIALS AND METHODS: Fifty Sprague-Dawley rats were used in this study. Polyethylene tubes were filled with Angelus WMTA, ProRoot WMTA, Bioaggregate, and Geristore. Empty control tubes were implanted into subcutaneous tissues and harvested at 7-, 14-, 28- and 60-day intervals. Tissue sections of 5 μm were stained with hematoxylin and eosin and observed under a light microscope. Inflammatory reactions were categorized as 0, none (without inflammatory cells); 1, mild (inflammatory cells ≤25); 2, moderate (25–125 inflammatory cells); and 3, severe (>125 inflammatory cells). Statistical analysis was performed with Kruskal-Wallis and Mann Whitney U tests. RESULTS: ProRoot WMTA and Angelus elicited significantly less inflammation than other materials (P<0.05). After 7 days, however, all the materials induced significantly more inflammation than the controls (P<0.05). Angelus-MTA group exhi-bited no significant differences from the Bioaggregate group (P=0.15); however, ProRoot WMTA elicited significantly less inflammation than Bioaggregate (P=0.02). Geristore induced significantly more inflammation than other groups (P<0.05). CONCLUSION: Geristore induced an inflammatory response higher than ProRoot WMTA; therefore, it is not recommended for clinical use.
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spelling pubmed-35932002013-03-13 Subcutaneous Connective Tissue Reactions to Various Endodontic Biomaterials: An Animal Study Saghiri, Mohammad Ali Tanideh, Nader Garcia-Godoy, Franklin Lotfi, Mehrdad Karamifar, Kasra Amanat, Dariush J Dent Res Dent Clin Dent Prospects Original Article BACKGROUND AND AIMS: Biocompatibility of root-end filling materials is a matter of debate. The aim of this study was to compare the biocompatibility of a variety of commercial ProRoot WMTA cements and a resin-based cement (Geristore®) with different pH values of setting reaction and different aluminum contents, implanted into the subcutaneous connective tissue of rats at various time intervals. MATERIALS AND METHODS: Fifty Sprague-Dawley rats were used in this study. Polyethylene tubes were filled with Angelus WMTA, ProRoot WMTA, Bioaggregate, and Geristore. Empty control tubes were implanted into subcutaneous tissues and harvested at 7-, 14-, 28- and 60-day intervals. Tissue sections of 5 μm were stained with hematoxylin and eosin and observed under a light microscope. Inflammatory reactions were categorized as 0, none (without inflammatory cells); 1, mild (inflammatory cells ≤25); 2, moderate (25–125 inflammatory cells); and 3, severe (>125 inflammatory cells). Statistical analysis was performed with Kruskal-Wallis and Mann Whitney U tests. RESULTS: ProRoot WMTA and Angelus elicited significantly less inflammation than other materials (P<0.05). After 7 days, however, all the materials induced significantly more inflammation than the controls (P<0.05). Angelus-MTA group exhi-bited no significant differences from the Bioaggregate group (P=0.15); however, ProRoot WMTA elicited significantly less inflammation than Bioaggregate (P=0.02). Geristore induced significantly more inflammation than other groups (P<0.05). CONCLUSION: Geristore induced an inflammatory response higher than ProRoot WMTA; therefore, it is not recommended for clinical use. Tabriz University of Medical Sciences 2013 2013-02-21 /pmc/articles/PMC3593200/ /pubmed/23486841 http://dx.doi.org/10.5681/joddd.2013.003 Text en © 2013 The Authors; Tabriz University of Medical Sciences http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Saghiri, Mohammad Ali
Tanideh, Nader
Garcia-Godoy, Franklin
Lotfi, Mehrdad
Karamifar, Kasra
Amanat, Dariush
Subcutaneous Connective Tissue Reactions to Various Endodontic Biomaterials: An Animal Study
title Subcutaneous Connective Tissue Reactions to Various Endodontic Biomaterials: An Animal Study
title_full Subcutaneous Connective Tissue Reactions to Various Endodontic Biomaterials: An Animal Study
title_fullStr Subcutaneous Connective Tissue Reactions to Various Endodontic Biomaterials: An Animal Study
title_full_unstemmed Subcutaneous Connective Tissue Reactions to Various Endodontic Biomaterials: An Animal Study
title_short Subcutaneous Connective Tissue Reactions to Various Endodontic Biomaterials: An Animal Study
title_sort subcutaneous connective tissue reactions to various endodontic biomaterials: an animal study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593200/
https://www.ncbi.nlm.nih.gov/pubmed/23486841
http://dx.doi.org/10.5681/joddd.2013.003
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