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Biocompatibility and mineralization potential of new calcium silicate cements

BACKGROUND/PURPOSE: As calcium silicate cements (CSCs) have been successfully used in various types of vital pulp therapy, many new CSC products have been developed. The aim of this study was to evaluate the biocompatibilities and mineralization potential of new CSC. The experimental materials were...

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Autores principales: Kim, Byurira, Lee, Yong-Hyuk, Kim, Ik-Hwan, Lee, Ko Eun, Kang, Chung-Min, Lee, Hyo-Seol, Choi, Hyung-Jun, Cheon, Kyounga, Song, Je Seon, Shin, Yooseok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Association for Dental Sciences of the Republic of China 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316440/
https://www.ncbi.nlm.nih.gov/pubmed/37404639
http://dx.doi.org/10.1016/j.jds.2022.10.004
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author Kim, Byurira
Lee, Yong-Hyuk
Kim, Ik-Hwan
Lee, Ko Eun
Kang, Chung-Min
Lee, Hyo-Seol
Choi, Hyung-Jun
Cheon, Kyounga
Song, Je Seon
Shin, Yooseok
author_facet Kim, Byurira
Lee, Yong-Hyuk
Kim, Ik-Hwan
Lee, Ko Eun
Kang, Chung-Min
Lee, Hyo-Seol
Choi, Hyung-Jun
Cheon, Kyounga
Song, Je Seon
Shin, Yooseok
author_sort Kim, Byurira
collection PubMed
description BACKGROUND/PURPOSE: As calcium silicate cements (CSCs) have been successfully used in various types of vital pulp therapy, many new CSC products have been developed. The aim of this study was to evaluate the biocompatibilities and mineralization potential of new CSC. The experimental materials were NeoMTA Plus and EndoSequence Root Repair Material-Fast Set Putty (ERRM-FS) which were compared to ProRoot MTA. MATERIALS AND METHODS: In vitro, the effects of the new CSC on stem cells were evaluated. Each CSC was prepared for cell viability testing, alkaline phosphatase (ALP) assay, and calcium ion release assay. In vivo, the exposed pulp model was used for the partial pulpotomy procedure. Thirty-six teeth were treated with three materials: ProRoot MTA, NeoMTA Plus, or ERRM-FS. After four weeks, the teeth were extracted and processed for histologic analysis. Dentin bridge formation, pulp inflammation, and odontoblastic cell layer were evaluated and the area of newly formed calcific barrier of each group was measured. RESULTS: Three CSCs demonstrated similar cell viability on stem cells and the levels of ALP and calcium release were not significantly different between tested materials. ProRoot MTA and ERRM-FS showed better tissue healing process than NeoMTA Plus after partial pulpotomy, in terms of quality of calcific barrier and pulp inflammation. The outcomes from measuring newly formed calcific area demonstrated no significant differences between the materials. CONCLUSION: NeoMTA Plus and ERRM-FS displayed similar biocompatibilities and mineralization potential compared to ProRoot MTA. Therefore, these new CSCs can be used as desirable alternatives to ProRoot MTA.
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spelling pubmed-103164402023-07-04 Biocompatibility and mineralization potential of new calcium silicate cements Kim, Byurira Lee, Yong-Hyuk Kim, Ik-Hwan Lee, Ko Eun Kang, Chung-Min Lee, Hyo-Seol Choi, Hyung-Jun Cheon, Kyounga Song, Je Seon Shin, Yooseok J Dent Sci Original Article BACKGROUND/PURPOSE: As calcium silicate cements (CSCs) have been successfully used in various types of vital pulp therapy, many new CSC products have been developed. The aim of this study was to evaluate the biocompatibilities and mineralization potential of new CSC. The experimental materials were NeoMTA Plus and EndoSequence Root Repair Material-Fast Set Putty (ERRM-FS) which were compared to ProRoot MTA. MATERIALS AND METHODS: In vitro, the effects of the new CSC on stem cells were evaluated. Each CSC was prepared for cell viability testing, alkaline phosphatase (ALP) assay, and calcium ion release assay. In vivo, the exposed pulp model was used for the partial pulpotomy procedure. Thirty-six teeth were treated with three materials: ProRoot MTA, NeoMTA Plus, or ERRM-FS. After four weeks, the teeth were extracted and processed for histologic analysis. Dentin bridge formation, pulp inflammation, and odontoblastic cell layer were evaluated and the area of newly formed calcific barrier of each group was measured. RESULTS: Three CSCs demonstrated similar cell viability on stem cells and the levels of ALP and calcium release were not significantly different between tested materials. ProRoot MTA and ERRM-FS showed better tissue healing process than NeoMTA Plus after partial pulpotomy, in terms of quality of calcific barrier and pulp inflammation. The outcomes from measuring newly formed calcific area demonstrated no significant differences between the materials. CONCLUSION: NeoMTA Plus and ERRM-FS displayed similar biocompatibilities and mineralization potential compared to ProRoot MTA. Therefore, these new CSCs can be used as desirable alternatives to ProRoot MTA. Association for Dental Sciences of the Republic of China 2023-07 2022-10-20 /pmc/articles/PMC10316440/ /pubmed/37404639 http://dx.doi.org/10.1016/j.jds.2022.10.004 Text en © 2022 Association for Dental Sciences of the Republic of China. Publishing services by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Kim, Byurira
Lee, Yong-Hyuk
Kim, Ik-Hwan
Lee, Ko Eun
Kang, Chung-Min
Lee, Hyo-Seol
Choi, Hyung-Jun
Cheon, Kyounga
Song, Je Seon
Shin, Yooseok
Biocompatibility and mineralization potential of new calcium silicate cements
title Biocompatibility and mineralization potential of new calcium silicate cements
title_full Biocompatibility and mineralization potential of new calcium silicate cements
title_fullStr Biocompatibility and mineralization potential of new calcium silicate cements
title_full_unstemmed Biocompatibility and mineralization potential of new calcium silicate cements
title_short Biocompatibility and mineralization potential of new calcium silicate cements
title_sort biocompatibility and mineralization potential of new calcium silicate cements
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316440/
https://www.ncbi.nlm.nih.gov/pubmed/37404639
http://dx.doi.org/10.1016/j.jds.2022.10.004
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