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Repair of the Orbital Wall Fractures in Rabbit Animal Model Using Nanostructured Hydroxyapatite-Based Implant
Cellular uptake and cytotoxicity of nanostructured hydroxyapatite (nanoHAp) are dependent on its physical parameters. Therefore, an understanding of both surface chemistry and morphology of nanoHAp is needed in order to be able to anticipate its in vivo behavior. The aim of this paper is to characte...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302541/ https://www.ncbi.nlm.nih.gov/pubmed/28344268 http://dx.doi.org/10.3390/nano6010011 |
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author | Gradinaru, Sinziana Popescu, Laura Madalina Piticescu, Roxana Mioara Zurac, Sabina Ciuluvica, Radu Burlacu, Alexandrina Tutuianu, Raluca Valsan, Sorina-Nicoleta Motoc, Adrian Mihail Voinea, Liliana Mary |
author_facet | Gradinaru, Sinziana Popescu, Laura Madalina Piticescu, Roxana Mioara Zurac, Sabina Ciuluvica, Radu Burlacu, Alexandrina Tutuianu, Raluca Valsan, Sorina-Nicoleta Motoc, Adrian Mihail Voinea, Liliana Mary |
author_sort | Gradinaru, Sinziana |
collection | PubMed |
description | Cellular uptake and cytotoxicity of nanostructured hydroxyapatite (nanoHAp) are dependent on its physical parameters. Therefore, an understanding of both surface chemistry and morphology of nanoHAp is needed in order to be able to anticipate its in vivo behavior. The aim of this paper is to characterize an engineered nanoHAp in terms of physico-chemical properties, biocompatibility, and its capability to reconstitute the orbital wall fractures in rabbits. NanoHAp was synthesized using a high pressure hydrothermal method and characterized by physico-chemical, structural, morphological, and optical techniques. X-ray diffraction revealed HAp crystallites of 21 nm, while Scanning Electron Microscopy (SEM) images showed spherical shapes of HAp powder. Mean particle size of HAp measured by DLS technique was 146.3 nm. Biocompatibility was estimated by the effect of HAp powder on the adhesion and proliferation of mesenchymal stem cells (MSC) in culture. The results showed that cell proliferation on powder-coated slides was between 73.4% and 98.3% of control cells (cells grown in normal culture conditions). Computed tomography analysis of the preformed nanoHAp implanted in orbital wall fractures, performed at one and two months postoperative, demonstrated the integration of the implants in the bones. In conclusion, our engineered nanoHAp is stable, biocompatible, and may be safely considered for reconstruction of orbital wall fractures. |
format | Online Article Text |
id | pubmed-5302541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-53025412017-03-21 Repair of the Orbital Wall Fractures in Rabbit Animal Model Using Nanostructured Hydroxyapatite-Based Implant Gradinaru, Sinziana Popescu, Laura Madalina Piticescu, Roxana Mioara Zurac, Sabina Ciuluvica, Radu Burlacu, Alexandrina Tutuianu, Raluca Valsan, Sorina-Nicoleta Motoc, Adrian Mihail Voinea, Liliana Mary Nanomaterials (Basel) Article Cellular uptake and cytotoxicity of nanostructured hydroxyapatite (nanoHAp) are dependent on its physical parameters. Therefore, an understanding of both surface chemistry and morphology of nanoHAp is needed in order to be able to anticipate its in vivo behavior. The aim of this paper is to characterize an engineered nanoHAp in terms of physico-chemical properties, biocompatibility, and its capability to reconstitute the orbital wall fractures in rabbits. NanoHAp was synthesized using a high pressure hydrothermal method and characterized by physico-chemical, structural, morphological, and optical techniques. X-ray diffraction revealed HAp crystallites of 21 nm, while Scanning Electron Microscopy (SEM) images showed spherical shapes of HAp powder. Mean particle size of HAp measured by DLS technique was 146.3 nm. Biocompatibility was estimated by the effect of HAp powder on the adhesion and proliferation of mesenchymal stem cells (MSC) in culture. The results showed that cell proliferation on powder-coated slides was between 73.4% and 98.3% of control cells (cells grown in normal culture conditions). Computed tomography analysis of the preformed nanoHAp implanted in orbital wall fractures, performed at one and two months postoperative, demonstrated the integration of the implants in the bones. In conclusion, our engineered nanoHAp is stable, biocompatible, and may be safely considered for reconstruction of orbital wall fractures. MDPI 2016-01-07 /pmc/articles/PMC5302541/ /pubmed/28344268 http://dx.doi.org/10.3390/nano6010011 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gradinaru, Sinziana Popescu, Laura Madalina Piticescu, Roxana Mioara Zurac, Sabina Ciuluvica, Radu Burlacu, Alexandrina Tutuianu, Raluca Valsan, Sorina-Nicoleta Motoc, Adrian Mihail Voinea, Liliana Mary Repair of the Orbital Wall Fractures in Rabbit Animal Model Using Nanostructured Hydroxyapatite-Based Implant |
title | Repair of the Orbital Wall Fractures in Rabbit Animal Model Using Nanostructured Hydroxyapatite-Based Implant |
title_full | Repair of the Orbital Wall Fractures in Rabbit Animal Model Using Nanostructured Hydroxyapatite-Based Implant |
title_fullStr | Repair of the Orbital Wall Fractures in Rabbit Animal Model Using Nanostructured Hydroxyapatite-Based Implant |
title_full_unstemmed | Repair of the Orbital Wall Fractures in Rabbit Animal Model Using Nanostructured Hydroxyapatite-Based Implant |
title_short | Repair of the Orbital Wall Fractures in Rabbit Animal Model Using Nanostructured Hydroxyapatite-Based Implant |
title_sort | repair of the orbital wall fractures in rabbit animal model using nanostructured hydroxyapatite-based implant |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302541/ https://www.ncbi.nlm.nih.gov/pubmed/28344268 http://dx.doi.org/10.3390/nano6010011 |
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