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The effect of green synthesis of TiO(2) nanoparticles/collagen/HA scaffold in bone regeneration: As an animal study
BACKGROUND: The bone defects cannot heal by themselves when their range exceeds the critical size defect (CSD). In clinical treatment, significant bone defects are often caused by trauma, developmental deformity, tumour resection and infection. OBJECTIVES: The purpose of this study was to investigat...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508526/ https://www.ncbi.nlm.nih.gov/pubmed/37485579 http://dx.doi.org/10.1002/vms3.1222 |
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author | Yazdanian, Alireza Jahandideh, Alireza Hesaraki, Saeed |
author_facet | Yazdanian, Alireza Jahandideh, Alireza Hesaraki, Saeed |
author_sort | Yazdanian, Alireza |
collection | PubMed |
description | BACKGROUND: The bone defects cannot heal by themselves when their range exceeds the critical size defect (CSD). In clinical treatment, significant bone defects are often caused by trauma, developmental deformity, tumour resection and infection. OBJECTIVES: The purpose of this study was to investigate the effect of green synthesis of TiO(2) from propolis extract/collagen/HA (Hydroxyapatite) scaffolds on bone regeneration in rats. METHODS: Water uptake, biodegradability, porosity and biodegradation of the scaffolds were evaluated after they were synthesised using freeze‐dry method. Cell viability by MTT assay was then evaluated. During the 4, 8 and 12 weeks following the scaffold implantation, the bone regeneration was evaluated using macroscopic and microscopic tests to determine the effectiveness of green synthesis of TiO(2) from propolis extract/collagen/HA scaffolds. RESULTS: Compared to the HA/Coll scaffold, ProTiO(2)/HA/Coll scaffold was reduced porosity, water absorption and degradability porosity. Based on in vitro tests, both synthetic scaffolds induced cell growth and were less toxic and stimulated cell growth. Based on histopathological testing, the ProTiO(2)/HA/Coll scaffolds formed high levels of bone during 12 weeks in comparison with HA/Coll and control group. CONCLUSIONS: ProTiO(2)/HA/Coll composite can be used in regenerative medicine, bone fillers and scaffolds. As a result, this research suggests that ProTiO(2)/HA/Coll composites could be promising candidates for bone regeneration. |
format | Online Article Text |
id | pubmed-10508526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105085262023-09-20 The effect of green synthesis of TiO(2) nanoparticles/collagen/HA scaffold in bone regeneration: As an animal study Yazdanian, Alireza Jahandideh, Alireza Hesaraki, Saeed Vet Med Sci OTHER BACKGROUND: The bone defects cannot heal by themselves when their range exceeds the critical size defect (CSD). In clinical treatment, significant bone defects are often caused by trauma, developmental deformity, tumour resection and infection. OBJECTIVES: The purpose of this study was to investigate the effect of green synthesis of TiO(2) from propolis extract/collagen/HA (Hydroxyapatite) scaffolds on bone regeneration in rats. METHODS: Water uptake, biodegradability, porosity and biodegradation of the scaffolds were evaluated after they were synthesised using freeze‐dry method. Cell viability by MTT assay was then evaluated. During the 4, 8 and 12 weeks following the scaffold implantation, the bone regeneration was evaluated using macroscopic and microscopic tests to determine the effectiveness of green synthesis of TiO(2) from propolis extract/collagen/HA scaffolds. RESULTS: Compared to the HA/Coll scaffold, ProTiO(2)/HA/Coll scaffold was reduced porosity, water absorption and degradability porosity. Based on in vitro tests, both synthetic scaffolds induced cell growth and were less toxic and stimulated cell growth. Based on histopathological testing, the ProTiO(2)/HA/Coll scaffolds formed high levels of bone during 12 weeks in comparison with HA/Coll and control group. CONCLUSIONS: ProTiO(2)/HA/Coll composite can be used in regenerative medicine, bone fillers and scaffolds. As a result, this research suggests that ProTiO(2)/HA/Coll composites could be promising candidates for bone regeneration. John Wiley and Sons Inc. 2023-07-22 /pmc/articles/PMC10508526/ /pubmed/37485579 http://dx.doi.org/10.1002/vms3.1222 Text en © 2023 The Authors. Veterinary Medicine and Science published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | OTHER Yazdanian, Alireza Jahandideh, Alireza Hesaraki, Saeed The effect of green synthesis of TiO(2) nanoparticles/collagen/HA scaffold in bone regeneration: As an animal study |
title | The effect of green synthesis of TiO(2) nanoparticles/collagen/HA scaffold in bone regeneration: As an animal study |
title_full | The effect of green synthesis of TiO(2) nanoparticles/collagen/HA scaffold in bone regeneration: As an animal study |
title_fullStr | The effect of green synthesis of TiO(2) nanoparticles/collagen/HA scaffold in bone regeneration: As an animal study |
title_full_unstemmed | The effect of green synthesis of TiO(2) nanoparticles/collagen/HA scaffold in bone regeneration: As an animal study |
title_short | The effect of green synthesis of TiO(2) nanoparticles/collagen/HA scaffold in bone regeneration: As an animal study |
title_sort | effect of green synthesis of tio(2) nanoparticles/collagen/ha scaffold in bone regeneration: as an animal study |
topic | OTHER |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508526/ https://www.ncbi.nlm.nih.gov/pubmed/37485579 http://dx.doi.org/10.1002/vms3.1222 |
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