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A novel dentin bonding scheme based on extrafibrillar demineralization combined with covalent adhesion using a dry-bonding technique

Dentin bonding is a dynamic process that involves the penetration of adhesive resin monomers into the extrafibrillar and intrafibrillar demineralized collagen matrix using a wet-bonding technique. However, adhesive resin monomers lack the capacity to infiltrate the intrafibrillar space, and the exce...

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Detalles Bibliográficos
Autores principales: Yu, F., Luo, M.L., Xu, R.C., Huang, L., Yu, H.H., Meng, M., Jia, J.Q., Hu, Z.H., Wu, W.Z., Tay, F.R., Xiao, Y.H., Niu, L.N., Chen, J.H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022110/
https://www.ncbi.nlm.nih.gov/pubmed/33842741
http://dx.doi.org/10.1016/j.bioactmat.2021.03.024
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author Yu, F.
Luo, M.L.
Xu, R.C.
Huang, L.
Yu, H.H.
Meng, M.
Jia, J.Q.
Hu, Z.H.
Wu, W.Z.
Tay, F.R.
Xiao, Y.H.
Niu, L.N.
Chen, J.H.
author_facet Yu, F.
Luo, M.L.
Xu, R.C.
Huang, L.
Yu, H.H.
Meng, M.
Jia, J.Q.
Hu, Z.H.
Wu, W.Z.
Tay, F.R.
Xiao, Y.H.
Niu, L.N.
Chen, J.H.
author_sort Yu, F.
collection PubMed
description Dentin bonding is a dynamic process that involves the penetration of adhesive resin monomers into the extrafibrillar and intrafibrillar demineralized collagen matrix using a wet-bonding technique. However, adhesive resin monomers lack the capacity to infiltrate the intrafibrillar space, and the excess water that is introduced by the wet-bonding technique remains at the bonding interface. This imperfectly bonded interface is inclined to hydrolytic degradation, severely jeopardizing the longevity of bonded clinical restorations. The present study introduces a dentin bonding scheme based on a dry-bonding technique, combined with the use of extrafibrillar demineralization and a collagen-reactive monomer (CRM)-based adhesive (CBA). Selective extrafibrillar demineralization was achieved using 1-wt% high-molecular weight (MW) carboxymethyl chitosan (CMCS) within a clinically acceptable timeframe to create a less aggressive bonding substance for dentin bonding due to its selectively extrafibrillar demineralization capacity. CMCS demineralization decreased the activation of in situ collagenase, improved the shrinking resistance of demineralized collagen, and thus provided stronger and more durable bonding than traditional phosphoric acid etching. The new dentin bonding scheme that contained CMCS and CBA and used a dry-bonding technique achieved an encouraging dentin bonding strength and durability with low technical sensitivity. This bonding scheme can be used to improve the stability of the resin-dentin interface and foster the longevity of bonded clinical restorations.
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spelling pubmed-80221102021-04-08 A novel dentin bonding scheme based on extrafibrillar demineralization combined with covalent adhesion using a dry-bonding technique Yu, F. Luo, M.L. Xu, R.C. Huang, L. Yu, H.H. Meng, M. Jia, J.Q. Hu, Z.H. Wu, W.Z. Tay, F.R. Xiao, Y.H. Niu, L.N. Chen, J.H. Bioact Mater Article Dentin bonding is a dynamic process that involves the penetration of adhesive resin monomers into the extrafibrillar and intrafibrillar demineralized collagen matrix using a wet-bonding technique. However, adhesive resin monomers lack the capacity to infiltrate the intrafibrillar space, and the excess water that is introduced by the wet-bonding technique remains at the bonding interface. This imperfectly bonded interface is inclined to hydrolytic degradation, severely jeopardizing the longevity of bonded clinical restorations. The present study introduces a dentin bonding scheme based on a dry-bonding technique, combined with the use of extrafibrillar demineralization and a collagen-reactive monomer (CRM)-based adhesive (CBA). Selective extrafibrillar demineralization was achieved using 1-wt% high-molecular weight (MW) carboxymethyl chitosan (CMCS) within a clinically acceptable timeframe to create a less aggressive bonding substance for dentin bonding due to its selectively extrafibrillar demineralization capacity. CMCS demineralization decreased the activation of in situ collagenase, improved the shrinking resistance of demineralized collagen, and thus provided stronger and more durable bonding than traditional phosphoric acid etching. The new dentin bonding scheme that contained CMCS and CBA and used a dry-bonding technique achieved an encouraging dentin bonding strength and durability with low technical sensitivity. This bonding scheme can be used to improve the stability of the resin-dentin interface and foster the longevity of bonded clinical restorations. KeAi Publishing 2021-03-23 /pmc/articles/PMC8022110/ /pubmed/33842741 http://dx.doi.org/10.1016/j.bioactmat.2021.03.024 Text en © 2021 The Authors http://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 Article
Yu, F.
Luo, M.L.
Xu, R.C.
Huang, L.
Yu, H.H.
Meng, M.
Jia, J.Q.
Hu, Z.H.
Wu, W.Z.
Tay, F.R.
Xiao, Y.H.
Niu, L.N.
Chen, J.H.
A novel dentin bonding scheme based on extrafibrillar demineralization combined with covalent adhesion using a dry-bonding technique
title A novel dentin bonding scheme based on extrafibrillar demineralization combined with covalent adhesion using a dry-bonding technique
title_full A novel dentin bonding scheme based on extrafibrillar demineralization combined with covalent adhesion using a dry-bonding technique
title_fullStr A novel dentin bonding scheme based on extrafibrillar demineralization combined with covalent adhesion using a dry-bonding technique
title_full_unstemmed A novel dentin bonding scheme based on extrafibrillar demineralization combined with covalent adhesion using a dry-bonding technique
title_short A novel dentin bonding scheme based on extrafibrillar demineralization combined with covalent adhesion using a dry-bonding technique
title_sort novel dentin bonding scheme based on extrafibrillar demineralization combined with covalent adhesion using a dry-bonding technique
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022110/
https://www.ncbi.nlm.nih.gov/pubmed/33842741
http://dx.doi.org/10.1016/j.bioactmat.2021.03.024
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