Cargando…
Bone regeneration using a porcine bone substitute collagen composite in vitro and in vivo
The biocharacteristics of xenogeneic grafts make them a possible substitute for autogenous bone grafts in dental bone graft procedures. This study aimed to develop a novel porcine graft with collagen capable of generating new bone in bone defects via osteoconduction over 8 weeks of healing and to co...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772614/ https://www.ncbi.nlm.nih.gov/pubmed/29343794 http://dx.doi.org/10.1038/s41598-018-19629-y |
_version_ | 1783293437304373248 |
---|---|
author | Salamanca, Eisner Hsu, Chia-Chen Huang, Haw-Ming Teng, Nai-Chia Lin, Che-Tong Pan, Yu-Hwa Chang, Wei-Jen |
author_facet | Salamanca, Eisner Hsu, Chia-Chen Huang, Haw-Ming Teng, Nai-Chia Lin, Che-Tong Pan, Yu-Hwa Chang, Wei-Jen |
author_sort | Salamanca, Eisner |
collection | PubMed |
description | The biocharacteristics of xenogeneic grafts make them a possible substitute for autogenous bone grafts in dental bone graft procedures. This study aimed to develop a novel porcine graft with collagen capable of generating new bone in bone defects via osteoconduction over 8 weeks of healing and to compare it with a porcine graft. The porcine collagen graft was made to undergo a cell viability test (MTT) and alkaline phosphatase assay (ALP). The surgical procedure was performed in 20 male adult New Zealand white rabbits. Four calvarial critical-size defects of 6 mm in diameter were prepared in each rabbit. The upper left defect was filled with a porcine graft of 500–1000 μm, the upper right with a porcine collagen graft, the lower left with hydroxyapatite/beta-tricalcium phosphate and the lower right served as the control without any filling material. The rabbits were divided and sacrificed at 2, 4, 6 and 8 weeks after surgery. Histological and micro-CT scan results showed that the performance of the porcine collagen graft is superior for regenerating new bone. Porcine collagen graft showed cell viability and osteoblast-like cell differentiation in vitro. The results indicate that porcine collagen graft is a potential bone substitute for clinical application. |
format | Online Article Text |
id | pubmed-5772614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57726142018-01-26 Bone regeneration using a porcine bone substitute collagen composite in vitro and in vivo Salamanca, Eisner Hsu, Chia-Chen Huang, Haw-Ming Teng, Nai-Chia Lin, Che-Tong Pan, Yu-Hwa Chang, Wei-Jen Sci Rep Article The biocharacteristics of xenogeneic grafts make them a possible substitute for autogenous bone grafts in dental bone graft procedures. This study aimed to develop a novel porcine graft with collagen capable of generating new bone in bone defects via osteoconduction over 8 weeks of healing and to compare it with a porcine graft. The porcine collagen graft was made to undergo a cell viability test (MTT) and alkaline phosphatase assay (ALP). The surgical procedure was performed in 20 male adult New Zealand white rabbits. Four calvarial critical-size defects of 6 mm in diameter were prepared in each rabbit. The upper left defect was filled with a porcine graft of 500–1000 μm, the upper right with a porcine collagen graft, the lower left with hydroxyapatite/beta-tricalcium phosphate and the lower right served as the control without any filling material. The rabbits were divided and sacrificed at 2, 4, 6 and 8 weeks after surgery. Histological and micro-CT scan results showed that the performance of the porcine collagen graft is superior for regenerating new bone. Porcine collagen graft showed cell viability and osteoblast-like cell differentiation in vitro. The results indicate that porcine collagen graft is a potential bone substitute for clinical application. Nature Publishing Group UK 2018-01-17 /pmc/articles/PMC5772614/ /pubmed/29343794 http://dx.doi.org/10.1038/s41598-018-19629-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Salamanca, Eisner Hsu, Chia-Chen Huang, Haw-Ming Teng, Nai-Chia Lin, Che-Tong Pan, Yu-Hwa Chang, Wei-Jen Bone regeneration using a porcine bone substitute collagen composite in vitro and in vivo |
title | Bone regeneration using a porcine bone substitute collagen composite in vitro and in vivo |
title_full | Bone regeneration using a porcine bone substitute collagen composite in vitro and in vivo |
title_fullStr | Bone regeneration using a porcine bone substitute collagen composite in vitro and in vivo |
title_full_unstemmed | Bone regeneration using a porcine bone substitute collagen composite in vitro and in vivo |
title_short | Bone regeneration using a porcine bone substitute collagen composite in vitro and in vivo |
title_sort | bone regeneration using a porcine bone substitute collagen composite in vitro and in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772614/ https://www.ncbi.nlm.nih.gov/pubmed/29343794 http://dx.doi.org/10.1038/s41598-018-19629-y |
work_keys_str_mv | AT salamancaeisner boneregenerationusingaporcinebonesubstitutecollagencompositeinvitroandinvivo AT hsuchiachen boneregenerationusingaporcinebonesubstitutecollagencompositeinvitroandinvivo AT huanghawming boneregenerationusingaporcinebonesubstitutecollagencompositeinvitroandinvivo AT tengnaichia boneregenerationusingaporcinebonesubstitutecollagencompositeinvitroandinvivo AT linchetong boneregenerationusingaporcinebonesubstitutecollagencompositeinvitroandinvivo AT panyuhwa boneregenerationusingaporcinebonesubstitutecollagencompositeinvitroandinvivo AT changweijen boneregenerationusingaporcinebonesubstitutecollagencompositeinvitroandinvivo |