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Multifunctional Lithium-Doped Mesoporous Nanoparticles for Effective Dentin Regeneration in vivo
INTRODUCTION: Effective infection control without irritating the pulp tissue is the key to successful vital pulp therapy. Developing a novel antibacterial biomaterial that promotes dentin regeneration for pulp capping is thus a promising strategy for enhancing vital pulp therapy. METHODS: Lithium-do...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516199/ https://www.ncbi.nlm.nih.gov/pubmed/37746049 http://dx.doi.org/10.2147/IJN.S424930 |
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author | Liang, Zitian Chen, Ding Jiang, Ye Su, Zhikang Pi, Yixing Luo, Tao Jiang, Qianzhou Yang, Li Guo, Lvhua |
author_facet | Liang, Zitian Chen, Ding Jiang, Ye Su, Zhikang Pi, Yixing Luo, Tao Jiang, Qianzhou Yang, Li Guo, Lvhua |
author_sort | Liang, Zitian |
collection | PubMed |
description | INTRODUCTION: Effective infection control without irritating the pulp tissue is the key to successful vital pulp therapy. Developing a novel antibacterial biomaterial that promotes dentin regeneration for pulp capping is thus a promising strategy for enhancing vital pulp therapy. METHODS: Lithium-doped mesoporous nanoparticles (Li-MNPs) were synthesized using an alkali-catalyzed sol-gel method. The particle size, elemental distribution, surface morphology, pore structure, and ion release from Li-MNPs were measured. Human dental pulp stem cells (hDPSCs) and Streptococcus mutans (S. mutans) were used to evaluate the biological effects of Li-MNPs. In addition, a dental pulp exposure mouse model was used to evaluate the regenerative effects of Li-MNPs. RESULTS: Li-MNPs had a larger surface area (221.18 m(2)/g), a larger pore volume (0.25 cm(3)/g), and a smaller particle size (520.92 ± 35.21 nm) than MNPs. The in vitro investigation demonstrated that Li-MNPs greatly enhanced the biomineralization and odontogenic differentiation of hDPSCs through the Wnt/β-catenin signaling pathway. Li-MNPs showed a strong antibacterial effect on S. mutans. As expected, Li-MNPs significantly promoted dentin regeneration in situ and in vivo. CONCLUSION: Li-MNPs promoted dentin regeneration and inhibited S. mutans growth, implying a possible application as a pulp capping agent in vital pulp therapy. |
format | Online Article Text |
id | pubmed-10516199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-105161992023-09-23 Multifunctional Lithium-Doped Mesoporous Nanoparticles for Effective Dentin Regeneration in vivo Liang, Zitian Chen, Ding Jiang, Ye Su, Zhikang Pi, Yixing Luo, Tao Jiang, Qianzhou Yang, Li Guo, Lvhua Int J Nanomedicine Original Research INTRODUCTION: Effective infection control without irritating the pulp tissue is the key to successful vital pulp therapy. Developing a novel antibacterial biomaterial that promotes dentin regeneration for pulp capping is thus a promising strategy for enhancing vital pulp therapy. METHODS: Lithium-doped mesoporous nanoparticles (Li-MNPs) were synthesized using an alkali-catalyzed sol-gel method. The particle size, elemental distribution, surface morphology, pore structure, and ion release from Li-MNPs were measured. Human dental pulp stem cells (hDPSCs) and Streptococcus mutans (S. mutans) were used to evaluate the biological effects of Li-MNPs. In addition, a dental pulp exposure mouse model was used to evaluate the regenerative effects of Li-MNPs. RESULTS: Li-MNPs had a larger surface area (221.18 m(2)/g), a larger pore volume (0.25 cm(3)/g), and a smaller particle size (520.92 ± 35.21 nm) than MNPs. The in vitro investigation demonstrated that Li-MNPs greatly enhanced the biomineralization and odontogenic differentiation of hDPSCs through the Wnt/β-catenin signaling pathway. Li-MNPs showed a strong antibacterial effect on S. mutans. As expected, Li-MNPs significantly promoted dentin regeneration in situ and in vivo. CONCLUSION: Li-MNPs promoted dentin regeneration and inhibited S. mutans growth, implying a possible application as a pulp capping agent in vital pulp therapy. Dove 2023-09-18 /pmc/articles/PMC10516199/ /pubmed/37746049 http://dx.doi.org/10.2147/IJN.S424930 Text en © 2023 Liang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Liang, Zitian Chen, Ding Jiang, Ye Su, Zhikang Pi, Yixing Luo, Tao Jiang, Qianzhou Yang, Li Guo, Lvhua Multifunctional Lithium-Doped Mesoporous Nanoparticles for Effective Dentin Regeneration in vivo |
title | Multifunctional Lithium-Doped Mesoporous Nanoparticles for Effective Dentin Regeneration in vivo |
title_full | Multifunctional Lithium-Doped Mesoporous Nanoparticles for Effective Dentin Regeneration in vivo |
title_fullStr | Multifunctional Lithium-Doped Mesoporous Nanoparticles for Effective Dentin Regeneration in vivo |
title_full_unstemmed | Multifunctional Lithium-Doped Mesoporous Nanoparticles for Effective Dentin Regeneration in vivo |
title_short | Multifunctional Lithium-Doped Mesoporous Nanoparticles for Effective Dentin Regeneration in vivo |
title_sort | multifunctional lithium-doped mesoporous nanoparticles for effective dentin regeneration in vivo |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516199/ https://www.ncbi.nlm.nih.gov/pubmed/37746049 http://dx.doi.org/10.2147/IJN.S424930 |
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