Cargando…
In-Vivo Efficacy of Compliant 3D Nano-Composite in Critical-Size Bone Defect Repair: a Six Month Preclinical Study in Rabbit
Bone defects above critical size do not heal completely by itself and thus represent major clinical challenge to reconstructive surgery. Numerous bone substitutes have already been used to promote bone regeneration, however their use, particularly for critical-sized bone defects along with their lon...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799616/ https://www.ncbi.nlm.nih.gov/pubmed/24204879 http://dx.doi.org/10.1371/journal.pone.0077578 |
_version_ | 1782287901557522432 |
---|---|
author | Sagar, Nitin Pandey, Alok K. Gurbani, Deepak Khan, Kainat Singh, Dhirendra Chaudhari, Bhushan P. Soni, Vivek P. Chattopadhyay, Naibedya Dhawan, Alok Bellare, Jayesh R. |
author_facet | Sagar, Nitin Pandey, Alok K. Gurbani, Deepak Khan, Kainat Singh, Dhirendra Chaudhari, Bhushan P. Soni, Vivek P. Chattopadhyay, Naibedya Dhawan, Alok Bellare, Jayesh R. |
author_sort | Sagar, Nitin |
collection | PubMed |
description | Bone defects above critical size do not heal completely by itself and thus represent major clinical challenge to reconstructive surgery. Numerous bone substitutes have already been used to promote bone regeneration, however their use, particularly for critical-sized bone defects along with their long term in vivo safety and efficacy remains a concern. The present study was designed to obtain a complete healing of critical-size defect made in the proximal tibia of New Zealand White rabbit, using nano-hydroxyapatite/gelatin and chemically carboxymethylated chitin (n-HA/gel/CMC) scaffold construct. The bone-implant interfaces and defect site healing was evaluated for a period up to 25 weeks using radiography, micro-computed tomography, fluorescence labeling, and histology and compared with respective SHAM (empty contra lateral control). The viscoelastic porous scaffold construct allows easy surgical insertion and post-operatively facilitate oxygenation and angiogenesis. Radiography of defect treated with scaffold construct suggested expedited healing at defect edges and within the defect site, unlike confined healing at edges of the SHAM sites. The architecture indices analyzed by micro-computed tomography showed a significant increase in percentage of bone volume fraction, resulted in reconciled cortico-trabecular bone formation at n-HA/gel/CMC constructs treated site (15.2% to 52.7%) when compared with respective SHAM (10.2% to 31.8%). Histological examination and fluorescence labeling revealed that the uniformly interconnected porous surface of scaffold construct enhanced osteoblasts’ activity and mineralization. These preclinical data suggest that, n-HA/gel/CMC construct exhibit stimulation of bone's innate regenerative capacity, thus underscoring their use in guided bone regeneration. |
format | Online Article Text |
id | pubmed-3799616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37996162013-11-07 In-Vivo Efficacy of Compliant 3D Nano-Composite in Critical-Size Bone Defect Repair: a Six Month Preclinical Study in Rabbit Sagar, Nitin Pandey, Alok K. Gurbani, Deepak Khan, Kainat Singh, Dhirendra Chaudhari, Bhushan P. Soni, Vivek P. Chattopadhyay, Naibedya Dhawan, Alok Bellare, Jayesh R. PLoS One Research Article Bone defects above critical size do not heal completely by itself and thus represent major clinical challenge to reconstructive surgery. Numerous bone substitutes have already been used to promote bone regeneration, however their use, particularly for critical-sized bone defects along with their long term in vivo safety and efficacy remains a concern. The present study was designed to obtain a complete healing of critical-size defect made in the proximal tibia of New Zealand White rabbit, using nano-hydroxyapatite/gelatin and chemically carboxymethylated chitin (n-HA/gel/CMC) scaffold construct. The bone-implant interfaces and defect site healing was evaluated for a period up to 25 weeks using radiography, micro-computed tomography, fluorescence labeling, and histology and compared with respective SHAM (empty contra lateral control). The viscoelastic porous scaffold construct allows easy surgical insertion and post-operatively facilitate oxygenation and angiogenesis. Radiography of defect treated with scaffold construct suggested expedited healing at defect edges and within the defect site, unlike confined healing at edges of the SHAM sites. The architecture indices analyzed by micro-computed tomography showed a significant increase in percentage of bone volume fraction, resulted in reconciled cortico-trabecular bone formation at n-HA/gel/CMC constructs treated site (15.2% to 52.7%) when compared with respective SHAM (10.2% to 31.8%). Histological examination and fluorescence labeling revealed that the uniformly interconnected porous surface of scaffold construct enhanced osteoblasts’ activity and mineralization. These preclinical data suggest that, n-HA/gel/CMC construct exhibit stimulation of bone's innate regenerative capacity, thus underscoring their use in guided bone regeneration. Public Library of Science 2013-10-18 /pmc/articles/PMC3799616/ /pubmed/24204879 http://dx.doi.org/10.1371/journal.pone.0077578 Text en © 2013 Sagar 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 Sagar, Nitin Pandey, Alok K. Gurbani, Deepak Khan, Kainat Singh, Dhirendra Chaudhari, Bhushan P. Soni, Vivek P. Chattopadhyay, Naibedya Dhawan, Alok Bellare, Jayesh R. In-Vivo Efficacy of Compliant 3D Nano-Composite in Critical-Size Bone Defect Repair: a Six Month Preclinical Study in Rabbit |
title |
In-Vivo Efficacy of Compliant 3D Nano-Composite in Critical-Size Bone Defect Repair: a Six Month Preclinical Study in Rabbit |
title_full |
In-Vivo Efficacy of Compliant 3D Nano-Composite in Critical-Size Bone Defect Repair: a Six Month Preclinical Study in Rabbit |
title_fullStr |
In-Vivo Efficacy of Compliant 3D Nano-Composite in Critical-Size Bone Defect Repair: a Six Month Preclinical Study in Rabbit |
title_full_unstemmed |
In-Vivo Efficacy of Compliant 3D Nano-Composite in Critical-Size Bone Defect Repair: a Six Month Preclinical Study in Rabbit |
title_short |
In-Vivo Efficacy of Compliant 3D Nano-Composite in Critical-Size Bone Defect Repair: a Six Month Preclinical Study in Rabbit |
title_sort | in-vivo efficacy of compliant 3d nano-composite in critical-size bone defect repair: a six month preclinical study in rabbit |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799616/ https://www.ncbi.nlm.nih.gov/pubmed/24204879 http://dx.doi.org/10.1371/journal.pone.0077578 |
work_keys_str_mv | AT sagarnitin invivoefficacyofcompliant3dnanocompositeincriticalsizebonedefectrepairasixmonthpreclinicalstudyinrabbit AT pandeyalokk invivoefficacyofcompliant3dnanocompositeincriticalsizebonedefectrepairasixmonthpreclinicalstudyinrabbit AT gurbanideepak invivoefficacyofcompliant3dnanocompositeincriticalsizebonedefectrepairasixmonthpreclinicalstudyinrabbit AT khankainat invivoefficacyofcompliant3dnanocompositeincriticalsizebonedefectrepairasixmonthpreclinicalstudyinrabbit AT singhdhirendra invivoefficacyofcompliant3dnanocompositeincriticalsizebonedefectrepairasixmonthpreclinicalstudyinrabbit AT chaudharibhushanp invivoefficacyofcompliant3dnanocompositeincriticalsizebonedefectrepairasixmonthpreclinicalstudyinrabbit AT sonivivekp invivoefficacyofcompliant3dnanocompositeincriticalsizebonedefectrepairasixmonthpreclinicalstudyinrabbit AT chattopadhyaynaibedya invivoefficacyofcompliant3dnanocompositeincriticalsizebonedefectrepairasixmonthpreclinicalstudyinrabbit AT dhawanalok invivoefficacyofcompliant3dnanocompositeincriticalsizebonedefectrepairasixmonthpreclinicalstudyinrabbit AT bellarejayeshr invivoefficacyofcompliant3dnanocompositeincriticalsizebonedefectrepairasixmonthpreclinicalstudyinrabbit |