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Mechanical Biocompatibility, Osteogenic Activity, and Antibacterial Efficacy of Calcium Silicate–Zirconia Biocomposites

[Image: see text] Zirconia ceramics with high mechanical properties have been used as a load-bearing implant in the dental and orthopedic surgery. However, poor bone bonding properties and high elastic modulus remain a challenge. Calcium silicate (CaSi)-based ceramic can foster osteoblast adhesion,...

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Autores principales: Ding, Shinn-Jyh, Chu, Ying-Hung, Chen, Pei-Tung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970563/
https://www.ncbi.nlm.nih.gov/pubmed/33748624
http://dx.doi.org/10.1021/acsomega.1c00097
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author Ding, Shinn-Jyh
Chu, Ying-Hung
Chen, Pei-Tung
author_facet Ding, Shinn-Jyh
Chu, Ying-Hung
Chen, Pei-Tung
author_sort Ding, Shinn-Jyh
collection PubMed
description [Image: see text] Zirconia ceramics with high mechanical properties have been used as a load-bearing implant in the dental and orthopedic surgery. However, poor bone bonding properties and high elastic modulus remain a challenge. Calcium silicate (CaSi)-based ceramic can foster osteoblast adhesion, growth, and differentiation and facilitate bone ingrowth. This study was to prepare CaSi-ZrO(2) composites and evaluate their mechanical properties, long-term stability, in vitro osteogenic activity, and antibacterial ability. The Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) bacteria and human mesenchymal stem cells (hMSCs) were used to evaluate the antibacterial and osteogenic activities of implants in vitro, respectively. Results indicated that the three-point bending strength of ZrO(2) was 486 MPa and Young’s modulus was 128 GPa, which were much higher than those of the cortical bone. In contrast, the bending strength and modulus of 20% (201 MPa and 48 GPa, respectively) and 30% CaSi (126 MPa and 20 GPa, respectively) composites were close to the reported strength and modulus of the cortical bone. As expected, higher CaSi content implants significantly enhanced cell growth, differentiation, and mineralization of hMSCs. It is interesting to note the induction ability of CaSi in osteogenic differentiation of hMSCs even when cultured in the absence of an osteogenic differentiation medium. The composite with the higher CaSi contents exhibited the greater bacteriostatic effect against E. coli and S. aureus. In conclusion, the addition of 20 wt % CaSi can effectively improve the mechanical biocompatibility, osteogenesis, and antibacterial activity of ZrO(2) ceramics, which may be a potential choice for load-bearing applications.
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spelling pubmed-79705632021-03-19 Mechanical Biocompatibility, Osteogenic Activity, and Antibacterial Efficacy of Calcium Silicate–Zirconia Biocomposites Ding, Shinn-Jyh Chu, Ying-Hung Chen, Pei-Tung ACS Omega [Image: see text] Zirconia ceramics with high mechanical properties have been used as a load-bearing implant in the dental and orthopedic surgery. However, poor bone bonding properties and high elastic modulus remain a challenge. Calcium silicate (CaSi)-based ceramic can foster osteoblast adhesion, growth, and differentiation and facilitate bone ingrowth. This study was to prepare CaSi-ZrO(2) composites and evaluate their mechanical properties, long-term stability, in vitro osteogenic activity, and antibacterial ability. The Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) bacteria and human mesenchymal stem cells (hMSCs) were used to evaluate the antibacterial and osteogenic activities of implants in vitro, respectively. Results indicated that the three-point bending strength of ZrO(2) was 486 MPa and Young’s modulus was 128 GPa, which were much higher than those of the cortical bone. In contrast, the bending strength and modulus of 20% (201 MPa and 48 GPa, respectively) and 30% CaSi (126 MPa and 20 GPa, respectively) composites were close to the reported strength and modulus of the cortical bone. As expected, higher CaSi content implants significantly enhanced cell growth, differentiation, and mineralization of hMSCs. It is interesting to note the induction ability of CaSi in osteogenic differentiation of hMSCs even when cultured in the absence of an osteogenic differentiation medium. The composite with the higher CaSi contents exhibited the greater bacteriostatic effect against E. coli and S. aureus. In conclusion, the addition of 20 wt % CaSi can effectively improve the mechanical biocompatibility, osteogenesis, and antibacterial activity of ZrO(2) ceramics, which may be a potential choice for load-bearing applications. American Chemical Society 2021-03-04 /pmc/articles/PMC7970563/ /pubmed/33748624 http://dx.doi.org/10.1021/acsomega.1c00097 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Ding, Shinn-Jyh
Chu, Ying-Hung
Chen, Pei-Tung
Mechanical Biocompatibility, Osteogenic Activity, and Antibacterial Efficacy of Calcium Silicate–Zirconia Biocomposites
title Mechanical Biocompatibility, Osteogenic Activity, and Antibacterial Efficacy of Calcium Silicate–Zirconia Biocomposites
title_full Mechanical Biocompatibility, Osteogenic Activity, and Antibacterial Efficacy of Calcium Silicate–Zirconia Biocomposites
title_fullStr Mechanical Biocompatibility, Osteogenic Activity, and Antibacterial Efficacy of Calcium Silicate–Zirconia Biocomposites
title_full_unstemmed Mechanical Biocompatibility, Osteogenic Activity, and Antibacterial Efficacy of Calcium Silicate–Zirconia Biocomposites
title_short Mechanical Biocompatibility, Osteogenic Activity, and Antibacterial Efficacy of Calcium Silicate–Zirconia Biocomposites
title_sort mechanical biocompatibility, osteogenic activity, and antibacterial efficacy of calcium silicate–zirconia biocomposites
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970563/
https://www.ncbi.nlm.nih.gov/pubmed/33748624
http://dx.doi.org/10.1021/acsomega.1c00097
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