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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...

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Autores principales: do Monte, Felipe A, Ahuja, Neelam, Awad, Kamal R, Pan, Zui, Young, Simon, Kim, Harry KW, Aswath, Pranesh, Brotto, Marco, Varanasi, Venu G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
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.
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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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