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Silicon Oxynitrophosphide Nanoscale Coating Enhances Antioxidant Marker‐Induced Angiogenesis During in vivo Cranial Bone‐Defect Healing
Critical‐sized bone defects are challenging to heal because of the sudden and large volume of lost bone. Fixative plates are often used to stabilize defects, yet oxidative stress and delayed angiogenesis are contributing factors to poor biocompatibility and delayed bone healing. This study tests the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046063/ https://www.ncbi.nlm.nih.gov/pubmed/33869985 http://dx.doi.org/10.1002/jbm4.10425 |
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author | do Monte, Felipe A Ahuja, Neelam Awad, Kamal R Pan, Zui Young, Simon Kim, Harry KW Aswath, Pranesh Brotto, Marco Varanasi, Venu G |
author_facet | do Monte, Felipe A Ahuja, Neelam Awad, Kamal R Pan, Zui Young, Simon Kim, Harry KW Aswath, Pranesh Brotto, Marco Varanasi, Venu G |
author_sort | do Monte, Felipe A |
collection | PubMed |
description | Critical‐sized bone defects are challenging to heal because of the sudden and large volume of lost bone. Fixative plates are often used to stabilize defects, yet oxidative stress and delayed angiogenesis are contributing factors to poor biocompatibility and delayed bone healing. This study tests the angiogenic and antioxidant properties of amorphous silicon oxynitrophosphide (SiONPx) nanoscale‐coating material on endothelial cells to regenerate vascular tissue in vitro and in bone defects. in vitro studies evaluate the effect of silicon oxynitride (SiONx) and two different SiONPx compositions on human endothelial cells exposed to ROS (eg, hydrogen peroxide) that simulates oxidative stress conditions. in vivo studies using adult male Sprague Dawley rats (approximately 450 g) were performed to compare a bare plate, a SiONPx‐coated implant plate, and a sham control group using a rat standard‐sized calvarial defect. Results from this study showed that plates coated with SiONPx significantly reduced cell death, and enhanced vascular tubule formation and matrix deposition by upregulating angiogenic and antioxidant expression (eg, vascular endothelial growth factor A, angiopoetin‐1, superoxide dismutase 1, nuclear factor erythroid 2‐related factor 2, and catalase 1). Moreover, endothelial cell markers (CD31) showed a significant tubular structure in the SiONPx coating group compared with an empty and uncoated plate group. This reveals that atomic doping of phosphate into the nanoscale coating of SiONx produced markedly elevated levels of antioxidant and angiogenic markers that enhance vascular tissue regeneration. This study found that SiONPx or SiONx nanoscale‐coated materials enhance antioxidant expression, angiogenic marker expression, and reduce ROS levels needed for accelerating vascular tissue regeneration. These results further suggest that SiONPx nanoscale coating could be a promising candidate for titanium plate for rapid and enhanced cranial bone‐defect healing. © 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC. on behalf of American Society for Bone and Mineral Research. |
format | Online Article Text |
id | pubmed-8046063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80460632021-04-16 Silicon Oxynitrophosphide Nanoscale Coating Enhances Antioxidant Marker‐Induced Angiogenesis During in vivo Cranial Bone‐Defect Healing do Monte, Felipe A Ahuja, Neelam Awad, Kamal R Pan, Zui Young, Simon Kim, Harry KW Aswath, Pranesh Brotto, Marco Varanasi, Venu G JBMR Plus Original Articles Critical‐sized bone defects are challenging to heal because of the sudden and large volume of lost bone. Fixative plates are often used to stabilize defects, yet oxidative stress and delayed angiogenesis are contributing factors to poor biocompatibility and delayed bone healing. This study tests the angiogenic and antioxidant properties of amorphous silicon oxynitrophosphide (SiONPx) nanoscale‐coating material on endothelial cells to regenerate vascular tissue in vitro and in bone defects. in vitro studies evaluate the effect of silicon oxynitride (SiONx) and two different SiONPx compositions on human endothelial cells exposed to ROS (eg, hydrogen peroxide) that simulates oxidative stress conditions. in vivo studies using adult male Sprague Dawley rats (approximately 450 g) were performed to compare a bare plate, a SiONPx‐coated implant plate, and a sham control group using a rat standard‐sized calvarial defect. Results from this study showed that plates coated with SiONPx significantly reduced cell death, and enhanced vascular tubule formation and matrix deposition by upregulating angiogenic and antioxidant expression (eg, vascular endothelial growth factor A, angiopoetin‐1, superoxide dismutase 1, nuclear factor erythroid 2‐related factor 2, and catalase 1). Moreover, endothelial cell markers (CD31) showed a significant tubular structure in the SiONPx coating group compared with an empty and uncoated plate group. This reveals that atomic doping of phosphate into the nanoscale coating of SiONx produced markedly elevated levels of antioxidant and angiogenic markers that enhance vascular tissue regeneration. This study found that SiONPx or SiONx nanoscale‐coated materials enhance antioxidant expression, angiogenic marker expression, and reduce ROS levels needed for accelerating vascular tissue regeneration. These results further suggest that SiONPx nanoscale coating could be a promising candidate for titanium plate for rapid and enhanced cranial bone‐defect healing. © 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC. on behalf of American Society for Bone and Mineral Research. John Wiley & Sons, Inc. 2021-03-18 /pmc/articles/PMC8046063/ /pubmed/33869985 http://dx.doi.org/10.1002/jbm4.10425 Text en © 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC. on behalf of American Society for Bone and Mineral Research. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles do Monte, Felipe A Ahuja, Neelam Awad, Kamal R Pan, Zui Young, Simon Kim, Harry KW Aswath, Pranesh Brotto, Marco Varanasi, Venu G Silicon Oxynitrophosphide Nanoscale Coating Enhances Antioxidant Marker‐Induced Angiogenesis During in vivo Cranial Bone‐Defect Healing |
title | Silicon Oxynitrophosphide Nanoscale Coating Enhances Antioxidant Marker‐Induced Angiogenesis During in vivo Cranial Bone‐Defect Healing |
title_full | Silicon Oxynitrophosphide Nanoscale Coating Enhances Antioxidant Marker‐Induced Angiogenesis During in vivo Cranial Bone‐Defect Healing |
title_fullStr | Silicon Oxynitrophosphide Nanoscale Coating Enhances Antioxidant Marker‐Induced Angiogenesis During in vivo Cranial Bone‐Defect Healing |
title_full_unstemmed | Silicon Oxynitrophosphide Nanoscale Coating Enhances Antioxidant Marker‐Induced Angiogenesis During in vivo Cranial Bone‐Defect Healing |
title_short | Silicon Oxynitrophosphide Nanoscale Coating Enhances Antioxidant Marker‐Induced Angiogenesis During in vivo Cranial Bone‐Defect Healing |
title_sort | silicon oxynitrophosphide nanoscale coating enhances antioxidant marker‐induced angiogenesis during in vivo cranial bone‐defect healing |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046063/ https://www.ncbi.nlm.nih.gov/pubmed/33869985 http://dx.doi.org/10.1002/jbm4.10425 |
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