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Investigation of dental elastomers as oral mucosa simulant materials

OBJECTIVE: To measure mechanical properties of dental soft liners in tensional stress to identify their suitability as human oral mucosa simulant materials. METHODS: Eleven different dental elastomers were subjected to tensile testing to obtain their tensile strength and elastic moduli (n = 15/group...

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Autores principales: Choi, Joanne Jung Eun, Chen, Shiyao, Waddell, John Neil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543465/
https://www.ncbi.nlm.nih.gov/pubmed/33512785
http://dx.doi.org/10.1002/cre2.399
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author Choi, Joanne Jung Eun
Chen, Shiyao
Waddell, John Neil
author_facet Choi, Joanne Jung Eun
Chen, Shiyao
Waddell, John Neil
author_sort Choi, Joanne Jung Eun
collection PubMed
description OBJECTIVE: To measure mechanical properties of dental soft liners in tensional stress to identify their suitability as human oral mucosa simulant materials. METHODS: Eleven different dental elastomers were subjected to tensile testing to obtain their tensile strength and elastic moduli (n = 15/group) according to the ISO‐527 method. Fractured surfaces of one specimen per sample group were examined under the light microscope and scanning electron microscope (SEM). Energy‐dispersive X‐ray spectroscopy (EDS) was performed for the elemental analysis or chemical characterization of each sample group. The obtained data were quantitatively and qualitatively analysed. They were also statistically analysed using SPSS version 25. RESULTS: The tensile strength of dental elastomers ranged from 0.43 MPa (±0.09) to 7.41 MPa (±1.11) and had statistically significant differences between tested groups (p = 0.001). Vertex soft heat‐cure soft liner, GC impression silicones and Silagum soft liners were found to have tensile strengths close to that of the oral mucosa reported by previous studies. SEM analysis revealed that the elastomers with higher filler contents showed rough fractured surface with plucking of particles after tensile fracture. CONCLUSION: This is the first study assessing the suitability of dental elastomers as human oral mucosa simulant materials which can be used for in vitro, mathematical modeling and finite element analysis (FEA) to study masticatory force distribution in oral mucosa. Out of 11 studied, six (Vertex Soft, GC heavy and Light body, Molloplast B, Algin X Ultra and Exaclear) dental elastomers showed similar mechanical properties to the Theil embalmed gingival tissues. Vertex Soft, GC Light body, and Molloplast B may be used for the majority of oral mucosal model when considering tensile strength as the primary factor for mechanical stimulation.
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spelling pubmed-85434652021-10-29 Investigation of dental elastomers as oral mucosa simulant materials Choi, Joanne Jung Eun Chen, Shiyao Waddell, John Neil Clin Exp Dent Res Original Articles OBJECTIVE: To measure mechanical properties of dental soft liners in tensional stress to identify their suitability as human oral mucosa simulant materials. METHODS: Eleven different dental elastomers were subjected to tensile testing to obtain their tensile strength and elastic moduli (n = 15/group) according to the ISO‐527 method. Fractured surfaces of one specimen per sample group were examined under the light microscope and scanning electron microscope (SEM). Energy‐dispersive X‐ray spectroscopy (EDS) was performed for the elemental analysis or chemical characterization of each sample group. The obtained data were quantitatively and qualitatively analysed. They were also statistically analysed using SPSS version 25. RESULTS: The tensile strength of dental elastomers ranged from 0.43 MPa (±0.09) to 7.41 MPa (±1.11) and had statistically significant differences between tested groups (p = 0.001). Vertex soft heat‐cure soft liner, GC impression silicones and Silagum soft liners were found to have tensile strengths close to that of the oral mucosa reported by previous studies. SEM analysis revealed that the elastomers with higher filler contents showed rough fractured surface with plucking of particles after tensile fracture. CONCLUSION: This is the first study assessing the suitability of dental elastomers as human oral mucosa simulant materials which can be used for in vitro, mathematical modeling and finite element analysis (FEA) to study masticatory force distribution in oral mucosa. Out of 11 studied, six (Vertex Soft, GC heavy and Light body, Molloplast B, Algin X Ultra and Exaclear) dental elastomers showed similar mechanical properties to the Theil embalmed gingival tissues. Vertex Soft, GC Light body, and Molloplast B may be used for the majority of oral mucosal model when considering tensile strength as the primary factor for mechanical stimulation. John Wiley and Sons Inc. 2021-01-29 /pmc/articles/PMC8543465/ /pubmed/33512785 http://dx.doi.org/10.1002/cre2.399 Text en © 2021 The Authors. Clinical and Experimental Dental Research published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Choi, Joanne Jung Eun
Chen, Shiyao
Waddell, John Neil
Investigation of dental elastomers as oral mucosa simulant materials
title Investigation of dental elastomers as oral mucosa simulant materials
title_full Investigation of dental elastomers as oral mucosa simulant materials
title_fullStr Investigation of dental elastomers as oral mucosa simulant materials
title_full_unstemmed Investigation of dental elastomers as oral mucosa simulant materials
title_short Investigation of dental elastomers as oral mucosa simulant materials
title_sort investigation of dental elastomers as oral mucosa simulant materials
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543465/
https://www.ncbi.nlm.nih.gov/pubmed/33512785
http://dx.doi.org/10.1002/cre2.399
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