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Bone Regeneration and Remodeling within a Unidirectional Porous Hydroxyapatite Bone Substitute at a Cortical Bone Defect Site: Histological Analysis at One and Two Years after Implantation

Unidirectional porous hydroxyapatite (UDPHAp) is an artificial bone substitute with a unique microstructure consisting of 100–300-µm oval pores that present the material unidirectionally. UDPHAp has a compression strength of 14 MPa and a porosity of 75%, which promotes cell migration and capillary f...

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Autores principales: Iwasashi, Masashi, Funayama, Toru, Watanabe, Arata, Noguchi, Hiroshi, Tsukanishi, Toshinori, Suetsugu, Yasushi, Makihara, Takeshi, Ochiai, Naoyuki, Yamazaki, Masashi, Sakane, Masataka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455501/
https://www.ncbi.nlm.nih.gov/pubmed/28793479
http://dx.doi.org/10.3390/ma8084884
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author Iwasashi, Masashi
Funayama, Toru
Watanabe, Arata
Noguchi, Hiroshi
Tsukanishi, Toshinori
Suetsugu, Yasushi
Makihara, Takeshi
Ochiai, Naoyuki
Yamazaki, Masashi
Sakane, Masataka
author_facet Iwasashi, Masashi
Funayama, Toru
Watanabe, Arata
Noguchi, Hiroshi
Tsukanishi, Toshinori
Suetsugu, Yasushi
Makihara, Takeshi
Ochiai, Naoyuki
Yamazaki, Masashi
Sakane, Masataka
author_sort Iwasashi, Masashi
collection PubMed
description Unidirectional porous hydroxyapatite (UDPHAp) is an artificial bone substitute with a unique microstructure consisting of 100–300-µm oval pores that present the material unidirectionally. UDPHAp has a compression strength of 14 MPa and a porosity of 75%, which promotes cell migration and capillary formation within the material. Despite these advantageous properties, bone remodeling and bone formation with UDPHAp remain unclear. To examine long-term remodeling and differences in bone formation based on the defect site, trapezoidal prism-shaped UDPHAp blocks were implanted into rectangular-shaped cortical bone defects in the proximal tibia of Japanese white rabbits. Histological analysis performed at 52 and 104 weeks after implantation revealed that bone and capillaries had formed within the implanted UDPHAp material. Bone formed within the UDPHAp implanted in the cortical defect of rabbit tibia and remodel up to two years. The percentage of new bone area within UDPHAp was larger in cortical lesions than that in medullary lesions. These findings suggest that UDPHAp is a promising material for the repair of non-critical-sized cortical bone defects.
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spelling pubmed-54555012017-07-28 Bone Regeneration and Remodeling within a Unidirectional Porous Hydroxyapatite Bone Substitute at a Cortical Bone Defect Site: Histological Analysis at One and Two Years after Implantation Iwasashi, Masashi Funayama, Toru Watanabe, Arata Noguchi, Hiroshi Tsukanishi, Toshinori Suetsugu, Yasushi Makihara, Takeshi Ochiai, Naoyuki Yamazaki, Masashi Sakane, Masataka Materials (Basel) Article Unidirectional porous hydroxyapatite (UDPHAp) is an artificial bone substitute with a unique microstructure consisting of 100–300-µm oval pores that present the material unidirectionally. UDPHAp has a compression strength of 14 MPa and a porosity of 75%, which promotes cell migration and capillary formation within the material. Despite these advantageous properties, bone remodeling and bone formation with UDPHAp remain unclear. To examine long-term remodeling and differences in bone formation based on the defect site, trapezoidal prism-shaped UDPHAp blocks were implanted into rectangular-shaped cortical bone defects in the proximal tibia of Japanese white rabbits. Histological analysis performed at 52 and 104 weeks after implantation revealed that bone and capillaries had formed within the implanted UDPHAp material. Bone formed within the UDPHAp implanted in the cortical defect of rabbit tibia and remodel up to two years. The percentage of new bone area within UDPHAp was larger in cortical lesions than that in medullary lesions. These findings suggest that UDPHAp is a promising material for the repair of non-critical-sized cortical bone defects. MDPI 2015-07-30 /pmc/articles/PMC5455501/ /pubmed/28793479 http://dx.doi.org/10.3390/ma8084884 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Iwasashi, Masashi
Funayama, Toru
Watanabe, Arata
Noguchi, Hiroshi
Tsukanishi, Toshinori
Suetsugu, Yasushi
Makihara, Takeshi
Ochiai, Naoyuki
Yamazaki, Masashi
Sakane, Masataka
Bone Regeneration and Remodeling within a Unidirectional Porous Hydroxyapatite Bone Substitute at a Cortical Bone Defect Site: Histological Analysis at One and Two Years after Implantation
title Bone Regeneration and Remodeling within a Unidirectional Porous Hydroxyapatite Bone Substitute at a Cortical Bone Defect Site: Histological Analysis at One and Two Years after Implantation
title_full Bone Regeneration and Remodeling within a Unidirectional Porous Hydroxyapatite Bone Substitute at a Cortical Bone Defect Site: Histological Analysis at One and Two Years after Implantation
title_fullStr Bone Regeneration and Remodeling within a Unidirectional Porous Hydroxyapatite Bone Substitute at a Cortical Bone Defect Site: Histological Analysis at One and Two Years after Implantation
title_full_unstemmed Bone Regeneration and Remodeling within a Unidirectional Porous Hydroxyapatite Bone Substitute at a Cortical Bone Defect Site: Histological Analysis at One and Two Years after Implantation
title_short Bone Regeneration and Remodeling within a Unidirectional Porous Hydroxyapatite Bone Substitute at a Cortical Bone Defect Site: Histological Analysis at One and Two Years after Implantation
title_sort bone regeneration and remodeling within a unidirectional porous hydroxyapatite bone substitute at a cortical bone defect site: histological analysis at one and two years after implantation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455501/
https://www.ncbi.nlm.nih.gov/pubmed/28793479
http://dx.doi.org/10.3390/ma8084884
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