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Article: GelMA/TCP nanocomposite scaffold for vital pulp therapy

TitleGelMA/TCP nanocomposite scaffold for vital pulp therapy
Authors
Issue Date7-Nov-2023
PublisherElsevier
Citation
Acta Biomaterialia, 2023 How to Cite?
Abstract

Pulp capping is a necessary procedure for preserving the vitality and health of the dental pulp, playing a crucial role in preventing the need for root canal treatment or tooth extraction. Here, we developed an electrospun gelatin methacryloyl (GelMA) fibrous scaffold incorporating beta-tricalcium phosphate (TCP) particles for pulp capping. A comprehensive morphological, physical-chemical, and mechanical characterization of the engineered fibrous scaffolds was performed. In vitro bioactivity, cell compatibility, and odontogenic differentiation potential of the scaffolds in dental pulp stem cells (DPSCs) were also evaluated. A pre-clinical in vivo model was used to determine the therapeutic role of the GelMA/TCP scaffolds in promoting hard tissue formation. Morphological, chemical, and thermal analyses confirmed effective TCP incorporation in the GelMA nanofibers. The GelMA+20%TCP nanofibrous scaffold exhibited bead-free morphology and suitable mechanical and degradation properties. In vitro, GelMA+20%TCP scaffolds supported apatite-like formation, improved cell spreading, and increased deposition of mineralization nodules. Gene expression analysis revealed upregulation of ALPLRUNX2, COL1A1, and DMP1 in the presence of TCP-laden scaffolds. In vivo, analyses showed mild inflammatory reaction upon scaffolds’ contact while supporting mineralized tissue formation. Although the levels of Nestin and DMP1 proteins did not exceed those associated with the clinical reference treatment (i.e., mineral trioxide aggregate), the GelMA+20%TCP scaffold exhibited comparable levels, thus suggesting the emergence of differentiated odontoblast-like cells capable of dentin matrix secretion. Our innovative GelMA/TCP scaffold represents a simplified and efficient alternative to conventional pulp-capping biomaterials.


Persistent Identifierhttp://hdl.handle.net/10722/339150
ISSN
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 1.925

 

DC FieldValueLanguage
dc.contributor.authorYuanyuan, Han-
dc.contributor.authorRenan, Dal-Fabbro-
dc.contributor.authorAbdel, H Mahmoud-
dc.contributor.authorMaedeh, Rahimnejad-
dc.contributor.authorJinping, Xu-
dc.contributor.authorMiguel, Castilho-
dc.contributor.authorWaruna, L Dissanayaka-
dc.contributor.authorMarco, C Bottino -
dc.date.accessioned2024-03-11T10:34:16Z-
dc.date.available2024-03-11T10:34:16Z-
dc.date.issued2023-11-07-
dc.identifier.citationActa Biomaterialia, 2023-
dc.identifier.issn1742-7061-
dc.identifier.urihttp://hdl.handle.net/10722/339150-
dc.description.abstract<p>Pulp capping is a necessary procedure for preserving the vitality and health of the dental pulp, playing a crucial role in preventing the need for root canal treatment or tooth extraction. Here, we developed an electrospun gelatin methacryloyl (GelMA) fibrous scaffold incorporating beta-tricalcium phosphate (TCP) particles for pulp capping. A comprehensive morphological, physical-chemical, and mechanical characterization of the engineered fibrous scaffolds was performed. <em>In vitro</em> bioactivity, cell compatibility, and odontogenic differentiation potential of the scaffolds in dental pulp stem cells (DPSCs) were also evaluated. A pre-clinical <em>in vivo</em> model was used to determine the therapeutic role of the GelMA/TCP scaffolds in promoting hard tissue formation. Morphological, chemical, and thermal analyses confirmed effective TCP incorporation in the GelMA <a href="https://www.sciencedirect.com/topics/materials-science/nanofiber" title="Learn more about nanofibers from ScienceDirect's AI-generated Topic Pages">nanofibers</a>. The GelMA+20%TCP nanofibrous scaffold exhibited bead-free morphology and suitable mechanical and degradation properties. <em>In vitro</em>, GelMA+20%TCP scaffolds supported apatite-like formation, improved cell spreading, and increased deposition of <a href="https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/mineralization" title="Learn more about mineralization from ScienceDirect's AI-generated Topic Pages">mineralization</a> nodules. <a href="https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/gene-expression-profiling" title="Learn more about Gene expression analysis from ScienceDirect's AI-generated Topic Pages">Gene expression analysis</a> revealed upregulation of <a href="https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/alpl" title="Learn more about ALPL from ScienceDirect's AI-generated Topic Pages">ALPL</a>, <a href="https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/runx2" title="Learn more about RUNX2 from ScienceDirect's AI-generated Topic Pages">RUNX2</a>, COL1A1, and DMP1 in the presence of TCP-laden scaffolds. <em>In vivo</em>, analyses showed mild inflammatory reaction upon scaffolds’ contact while supporting <a href="https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/mineralized-tissue" title="Learn more about mineralized tissue from ScienceDirect's AI-generated Topic Pages">mineralized tissue</a> formation. Although the levels of Nestin and DMP1 proteins did not exceed those associated with the clinical reference treatment (i.e., mineral trioxide aggregate), the GelMA+20%TCP scaffold exhibited comparable levels, thus suggesting the emergence of differentiated odontoblast-like cells capable of dentin matrix secretion. Our innovative GelMA/TCP scaffold represents a simplified and efficient alternative to conventional pulp-capping biomaterials.</p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofActa Biomaterialia-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleGelMA/TCP nanocomposite scaffold for vital pulp therapy-
dc.typeArticle-
dc.identifier.doi10.1016/j.actbio.2023.11.005-
dc.identifier.eissn1878-7568-
dc.identifier.issnl1742-7061-

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