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Pulp regeneration with hemostatic matrices as a scaffold in an immature tooth minipig model
Control of blood clotting in root canal systems is one of the most critical and difficult concerns for regenerative endodontics therapy (RET). The purpose of this study was to investigate the effects of using gelatin- and fibrin-based hemostatic hydrogels as a scaffold on pulp regeneration in a mini...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385085/ https://www.ncbi.nlm.nih.gov/pubmed/32719323 http://dx.doi.org/10.1038/s41598-020-69437-6 |
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author | Jang, Ji-Hyun Moon, Joung-Ho Kim, Sahng Gyoon Kim, Sun-Young |
author_facet | Jang, Ji-Hyun Moon, Joung-Ho Kim, Sahng Gyoon Kim, Sun-Young |
author_sort | Jang, Ji-Hyun |
collection | PubMed |
description | Control of blood clotting in root canal systems is one of the most critical and difficult concerns for regenerative endodontics therapy (RET). The purpose of this study was to investigate the effects of using gelatin- and fibrin-based hemostatic hydrogels as a scaffold on pulp regeneration in a minipig model. Cell viability of human dental pulp stem cells cultured three-dimensionally in gelatin-based and fibrin-based scaffolds was evaluated by MTT and live/dead assay. RET was performed on 24 immature premolars with an autologous blood clot (PC), gelatin-based and fibrin-based hemostatic matrices (GM and FM), or without the insertion of a scaffold (NC). The follow-up period was 12 weeks. Radiographic and histologic assessments for pulp regeneration were performed. Gelatin-based scaffolds exhibited significantly higher cell viability than fibrin-based scaffolds after 15 days (P < 0.05). The PC and GM groups showed favorable root development without inflammation and newly mineralized tissue deposited in the root canal system, while FM group presented inflammatory changes with the continuation of root development. The NC group exhibited internal root resorption with periapical lesions. The application of GM in RET led to favorable clinical outcomes of root development without inflammatory changes compared to conventional RET. Our results suggest that GM may serve as a viable regenerative scaffold for pulp regeneration. |
format | Online Article Text |
id | pubmed-7385085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73850852020-07-28 Pulp regeneration with hemostatic matrices as a scaffold in an immature tooth minipig model Jang, Ji-Hyun Moon, Joung-Ho Kim, Sahng Gyoon Kim, Sun-Young Sci Rep Article Control of blood clotting in root canal systems is one of the most critical and difficult concerns for regenerative endodontics therapy (RET). The purpose of this study was to investigate the effects of using gelatin- and fibrin-based hemostatic hydrogels as a scaffold on pulp regeneration in a minipig model. Cell viability of human dental pulp stem cells cultured three-dimensionally in gelatin-based and fibrin-based scaffolds was evaluated by MTT and live/dead assay. RET was performed on 24 immature premolars with an autologous blood clot (PC), gelatin-based and fibrin-based hemostatic matrices (GM and FM), or without the insertion of a scaffold (NC). The follow-up period was 12 weeks. Radiographic and histologic assessments for pulp regeneration were performed. Gelatin-based scaffolds exhibited significantly higher cell viability than fibrin-based scaffolds after 15 days (P < 0.05). The PC and GM groups showed favorable root development without inflammation and newly mineralized tissue deposited in the root canal system, while FM group presented inflammatory changes with the continuation of root development. The NC group exhibited internal root resorption with periapical lesions. The application of GM in RET led to favorable clinical outcomes of root development without inflammatory changes compared to conventional RET. Our results suggest that GM may serve as a viable regenerative scaffold for pulp regeneration. Nature Publishing Group UK 2020-07-27 /pmc/articles/PMC7385085/ /pubmed/32719323 http://dx.doi.org/10.1038/s41598-020-69437-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jang, Ji-Hyun Moon, Joung-Ho Kim, Sahng Gyoon Kim, Sun-Young Pulp regeneration with hemostatic matrices as a scaffold in an immature tooth minipig model |
title | Pulp regeneration with hemostatic matrices as a scaffold in an immature tooth minipig model |
title_full | Pulp regeneration with hemostatic matrices as a scaffold in an immature tooth minipig model |
title_fullStr | Pulp regeneration with hemostatic matrices as a scaffold in an immature tooth minipig model |
title_full_unstemmed | Pulp regeneration with hemostatic matrices as a scaffold in an immature tooth minipig model |
title_short | Pulp regeneration with hemostatic matrices as a scaffold in an immature tooth minipig model |
title_sort | pulp regeneration with hemostatic matrices as a scaffold in an immature tooth minipig model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385085/ https://www.ncbi.nlm.nih.gov/pubmed/32719323 http://dx.doi.org/10.1038/s41598-020-69437-6 |
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