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Osteogenic Properties of PBLG-g-HA/PLLA Nanocomposites
New development of biomaterial scaffolds remains a prominent issue for the regeneration of lost or fractured bone. Of these scaffolds, a number of bioactive polymers have been synthesized and fabricated for diverse biological roles. Although recent evidence has demonstrated that composite scaffolds...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153559/ https://www.ncbi.nlm.nih.gov/pubmed/25184285 http://dx.doi.org/10.1371/journal.pone.0105876 |
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author | Liao, Lan Yang, Shuang Miron, Richard J. Wei, Junchao Zhang, Yufeng Zhang, Meng |
author_facet | Liao, Lan Yang, Shuang Miron, Richard J. Wei, Junchao Zhang, Yufeng Zhang, Meng |
author_sort | Liao, Lan |
collection | PubMed |
description | New development of biomaterial scaffolds remains a prominent issue for the regeneration of lost or fractured bone. Of these scaffolds, a number of bioactive polymers have been synthesized and fabricated for diverse biological roles. Although recent evidence has demonstrated that composite scaffolds such as HA/PLLA have improved properties when compared to either HA or PLLA alone, recent investigations have demonstrated that the phase compatibility between HA and PLLA layers is weak preventing optimal enhancement of the mechanical properties and making the composites prone to breakdown. In the present study, poly (γ-benzyl-L-glutamate) modified hydroxyapatite/(poly (L-lactic acid)) (PBLG-g-HA/PLLA) composite scaffolds were fabricated with improved phase compatibility and tested for their osteogenic properties in 18 Wistar female rats by analyzing new bone formation in 3 mm bilateral femur defects in vivo. At time points, 2, 4 and 8 weeks post surgery, bone formation was evaluated by µ-CT and histological analysis by comparing 4 treatment groups; 1) blank defect, 2) PLLA, 3) HA/PLLA and 4) PBLG-g-HA/PLLA scaffolds. The in vivo analysis demonstrated that new bone formation was much more prominent in HA/PLLA and PBLG-g-HA/PLLA groups as depicted by µ-CT, H&E staining and immunohistochemistry for collagen I. TRAP staining was also utilized to determine the influence of osteoclast cell number and staining intensity to the various scaffolds. No significant differences in either staining intensity or osteoclast numbers between all treatment modalities was observed, however blank defects did contain a higher number of osteoclast-like cells. The results from the present study illustrate the potential of PBLG-g-HA/PLLA scaffolds for bone tissue engineering applications by demonstrating favorable osteogenic properties. |
format | Online Article Text |
id | pubmed-4153559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41535592014-09-05 Osteogenic Properties of PBLG-g-HA/PLLA Nanocomposites Liao, Lan Yang, Shuang Miron, Richard J. Wei, Junchao Zhang, Yufeng Zhang, Meng PLoS One Research Article New development of biomaterial scaffolds remains a prominent issue for the regeneration of lost or fractured bone. Of these scaffolds, a number of bioactive polymers have been synthesized and fabricated for diverse biological roles. Although recent evidence has demonstrated that composite scaffolds such as HA/PLLA have improved properties when compared to either HA or PLLA alone, recent investigations have demonstrated that the phase compatibility between HA and PLLA layers is weak preventing optimal enhancement of the mechanical properties and making the composites prone to breakdown. In the present study, poly (γ-benzyl-L-glutamate) modified hydroxyapatite/(poly (L-lactic acid)) (PBLG-g-HA/PLLA) composite scaffolds were fabricated with improved phase compatibility and tested for their osteogenic properties in 18 Wistar female rats by analyzing new bone formation in 3 mm bilateral femur defects in vivo. At time points, 2, 4 and 8 weeks post surgery, bone formation was evaluated by µ-CT and histological analysis by comparing 4 treatment groups; 1) blank defect, 2) PLLA, 3) HA/PLLA and 4) PBLG-g-HA/PLLA scaffolds. The in vivo analysis demonstrated that new bone formation was much more prominent in HA/PLLA and PBLG-g-HA/PLLA groups as depicted by µ-CT, H&E staining and immunohistochemistry for collagen I. TRAP staining was also utilized to determine the influence of osteoclast cell number and staining intensity to the various scaffolds. No significant differences in either staining intensity or osteoclast numbers between all treatment modalities was observed, however blank defects did contain a higher number of osteoclast-like cells. The results from the present study illustrate the potential of PBLG-g-HA/PLLA scaffolds for bone tissue engineering applications by demonstrating favorable osteogenic properties. Public Library of Science 2014-09-03 /pmc/articles/PMC4153559/ /pubmed/25184285 http://dx.doi.org/10.1371/journal.pone.0105876 Text en © 2014 Liao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Liao, Lan Yang, Shuang Miron, Richard J. Wei, Junchao Zhang, Yufeng Zhang, Meng Osteogenic Properties of PBLG-g-HA/PLLA Nanocomposites |
title | Osteogenic Properties of PBLG-g-HA/PLLA Nanocomposites |
title_full | Osteogenic Properties of PBLG-g-HA/PLLA Nanocomposites |
title_fullStr | Osteogenic Properties of PBLG-g-HA/PLLA Nanocomposites |
title_full_unstemmed | Osteogenic Properties of PBLG-g-HA/PLLA Nanocomposites |
title_short | Osteogenic Properties of PBLG-g-HA/PLLA Nanocomposites |
title_sort | osteogenic properties of pblg-g-ha/plla nanocomposites |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153559/ https://www.ncbi.nlm.nih.gov/pubmed/25184285 http://dx.doi.org/10.1371/journal.pone.0105876 |
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