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https://hdl.handle.net/2445/219233
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DC Field | Value | Language |
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dc.contributor.author | Belkadi, Roumaissa | - |
dc.contributor.author | Sanz-Serrano, Diana | - |
dc.contributor.author | Ventura Pujol, Francesc | - |
dc.contributor.author | Mercadé Bellido, Montserrat | - |
dc.date.accessioned | 2025-02-25T13:31:04Z | - |
dc.date.available | 2025-02-25T13:31:04Z | - |
dc.date.issued | 2024-10-01 | - |
dc.identifier.issn | 0143-2885 | - |
dc.identifier.uri | https://hdl.handle.net/2445/219233 | - |
dc.description.abstract | Background: The dental pulp's environment is essential for the regulation of mesenchymal stem cells' homeostasis and thus, it is of great importance to evaluate the materials used in regenerative procedures. Aim: To assess in vitro (i) the effect of chitosan nanoparticles, 0.2% chitosan irrigation solution, Dual Rinse®, 17% EDTA, 10% citric acid and 2.5% NaOCl on DSCS viability; (ii) the effect of different concentrations of TGF-β1 on DCSC proliferation; and (iii) whether treatment with TGF-β1 following exposure to the different irrigation solutions could compensate for their negative effects. Methodology: (i) DSCS were treated with three dilutions (1:10, 1:100 and 1:1000) of the six irrigation solutions prepared in DMEM for 10 and 60min to assess the effect on viability. (ii) The effect of different concentrations (0, 1, 5 and 10ng/mL) of TGFβ1 on DCSC proliferation was assessed at 1, 3 and 7days. (iii) The proliferative effect of TGF-β1 following 10-min exposure to 1:10 dilution of each irrigation solution was also tested. We used MTT assay to assess viability and proliferation. We performed statistical analysis using Prism software. Results: (i) The different endodontic irrigation solutions tested showed a significant effect on cell viability (p≤.0001). Significant interactions between the endodontic irrigation solutions and their dilutions were also found for all parameters (p≤.0001). Chitosan nanoparticles and 0.2% chitosan irrigation solution were the least cytotoxic to DSCS whilst 2.5% NaOCl was the most cytotoxic followed by 17% EDTA. (ii) TGF-β1 at concentrations of 1 and 5ng/mL resulted in significantly higher proliferation compared to the control group. (iii) Exposure to 17% EDTA or 2.5% NaOCl for 10min was sufficient to make DSCS cells refractory to the proliferative effects of TGF-β1. DSCS groups treated with TGF-β1 following exposure to chitosan nanoparticles, 0.2% chitosan irrigation solution. | - |
dc.format.extent | 13 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | John Wiley & Sons | - |
dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.1111/iej.14112 | - |
dc.relation.ispartof | International Endodontic Journal, 2024, vol. 57, num.10, p. 1942-1504 | - |
dc.relation.uri | https://doi.org/10.1111/iej.14112 | - |
dc.rights | cc by-nc-nd (c) Belkadi, Roumaissa et al., 2024 | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | - |
dc.source | Articles publicats en revistes (Odontoestomatologia) | - |
dc.subject.classification | Proliferació cel·lular | - |
dc.subject.classification | Quitosan | - |
dc.subject.classification | Polpa dental | - |
dc.subject.other | Cell proliferation | - |
dc.subject.other | Chitosan | - |
dc.subject.other | Dental pulp | - |
dc.title | Chitosan-based endodontic irrigation solutions and TGF-β1 treatment: Creating the most favourable environment for the survival and proliferation of stem cells of the apical papilla in vitro | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.identifier.idgrec | 749087 | - |
dc.date.updated | 2025-02-25T13:31:04Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
dc.identifier.pmid | 38888363 | - |
Appears in Collections: | Articles publicats en revistes (Odontoestomatologia) Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) |
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862170.pdf | 1.82 MB | Adobe PDF | View/Open |
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