Cargando…

Incorporation of Chitosan Microspheres into Collagen-Chitosan Scaffolds for the Controlled Release of Nerve Growth Factor

BACKGROUND: Artifical nerve scaffold can be used as a promising alternative to autologous nerve grafts to enhance the repair of peripheral nerve defects. However, current nerve scaffolds lack efficient microstructure and neurotrophic support. METHODS: Microsphere–Scaffold composite was developed by...

Descripción completa

Detalles Bibliográficos
Autores principales: Zeng, Wen, Rong, Mengyao, Hu, Xueyu, Xiao, Wei, Qi, Fengyu, Huang, Jinghui, Luo, Zhuojing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077743/
https://www.ncbi.nlm.nih.gov/pubmed/24983464
http://dx.doi.org/10.1371/journal.pone.0101300
_version_ 1782323644331982848
author Zeng, Wen
Rong, Mengyao
Hu, Xueyu
Xiao, Wei
Qi, Fengyu
Huang, Jinghui
Luo, Zhuojing
author_facet Zeng, Wen
Rong, Mengyao
Hu, Xueyu
Xiao, Wei
Qi, Fengyu
Huang, Jinghui
Luo, Zhuojing
author_sort Zeng, Wen
collection PubMed
description BACKGROUND: Artifical nerve scaffold can be used as a promising alternative to autologous nerve grafts to enhance the repair of peripheral nerve defects. However, current nerve scaffolds lack efficient microstructure and neurotrophic support. METHODS: Microsphere–Scaffold composite was developed by incorporating chitosan microspheres loaded with nerve growth factor (NGF–CMSs) into collagen-chitosan scaffolds (CCH) with longitudinally oriented microchannels (NGF–CMSs/CCH). The morphological characterizations, in vitro release kinetics study, neurite outgrowth assay, and bioactivity assay were evaluated. After that, a 15-mm-long sciatic nerve gap in rats was bridged by the NGF–CMSs/CCH, CCH physically absorbed NGF (NGF/CCH), CCH or nerve autograft. 16 weeks after implantation, electrophysiology, fluoro-gold retrograde tracing, and nerve morphometry were performed. RESULTS: The NGF–CMSs were evenly distributed throughout the longitudinally oriented microchannels of the scaffold. The NGF–CMSs/CCH was capable of sustained release of bioactive NGF within 28 days as compared with others in vitro. In vivo animal study demonstrated that the outcomes of NGF–CMSs/CCH were better than those of NGF/CCH or CCH. CONCLUSION: Our findings suggest that incorporation of NGF–CMSs into the CCH may be a promising tool in the repair of peripheral nerve defects.
format Online
Article
Text
id pubmed-4077743
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-40777432014-07-03 Incorporation of Chitosan Microspheres into Collagen-Chitosan Scaffolds for the Controlled Release of Nerve Growth Factor Zeng, Wen Rong, Mengyao Hu, Xueyu Xiao, Wei Qi, Fengyu Huang, Jinghui Luo, Zhuojing PLoS One Research Article BACKGROUND: Artifical nerve scaffold can be used as a promising alternative to autologous nerve grafts to enhance the repair of peripheral nerve defects. However, current nerve scaffolds lack efficient microstructure and neurotrophic support. METHODS: Microsphere–Scaffold composite was developed by incorporating chitosan microspheres loaded with nerve growth factor (NGF–CMSs) into collagen-chitosan scaffolds (CCH) with longitudinally oriented microchannels (NGF–CMSs/CCH). The morphological characterizations, in vitro release kinetics study, neurite outgrowth assay, and bioactivity assay were evaluated. After that, a 15-mm-long sciatic nerve gap in rats was bridged by the NGF–CMSs/CCH, CCH physically absorbed NGF (NGF/CCH), CCH or nerve autograft. 16 weeks after implantation, electrophysiology, fluoro-gold retrograde tracing, and nerve morphometry were performed. RESULTS: The NGF–CMSs were evenly distributed throughout the longitudinally oriented microchannels of the scaffold. The NGF–CMSs/CCH was capable of sustained release of bioactive NGF within 28 days as compared with others in vitro. In vivo animal study demonstrated that the outcomes of NGF–CMSs/CCH were better than those of NGF/CCH or CCH. CONCLUSION: Our findings suggest that incorporation of NGF–CMSs into the CCH may be a promising tool in the repair of peripheral nerve defects. Public Library of Science 2014-07-01 /pmc/articles/PMC4077743/ /pubmed/24983464 http://dx.doi.org/10.1371/journal.pone.0101300 Text en © 2014 Zeng 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
Zeng, Wen
Rong, Mengyao
Hu, Xueyu
Xiao, Wei
Qi, Fengyu
Huang, Jinghui
Luo, Zhuojing
Incorporation of Chitosan Microspheres into Collagen-Chitosan Scaffolds for the Controlled Release of Nerve Growth Factor
title Incorporation of Chitosan Microspheres into Collagen-Chitosan Scaffolds for the Controlled Release of Nerve Growth Factor
title_full Incorporation of Chitosan Microspheres into Collagen-Chitosan Scaffolds for the Controlled Release of Nerve Growth Factor
title_fullStr Incorporation of Chitosan Microspheres into Collagen-Chitosan Scaffolds for the Controlled Release of Nerve Growth Factor
title_full_unstemmed Incorporation of Chitosan Microspheres into Collagen-Chitosan Scaffolds for the Controlled Release of Nerve Growth Factor
title_short Incorporation of Chitosan Microspheres into Collagen-Chitosan Scaffolds for the Controlled Release of Nerve Growth Factor
title_sort incorporation of chitosan microspheres into collagen-chitosan scaffolds for the controlled release of nerve growth factor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077743/
https://www.ncbi.nlm.nih.gov/pubmed/24983464
http://dx.doi.org/10.1371/journal.pone.0101300
work_keys_str_mv AT zengwen incorporationofchitosanmicrospheresintocollagenchitosanscaffoldsforthecontrolledreleaseofnervegrowthfactor
AT rongmengyao incorporationofchitosanmicrospheresintocollagenchitosanscaffoldsforthecontrolledreleaseofnervegrowthfactor
AT huxueyu incorporationofchitosanmicrospheresintocollagenchitosanscaffoldsforthecontrolledreleaseofnervegrowthfactor
AT xiaowei incorporationofchitosanmicrospheresintocollagenchitosanscaffoldsforthecontrolledreleaseofnervegrowthfactor
AT qifengyu incorporationofchitosanmicrospheresintocollagenchitosanscaffoldsforthecontrolledreleaseofnervegrowthfactor
AT huangjinghui incorporationofchitosanmicrospheresintocollagenchitosanscaffoldsforthecontrolledreleaseofnervegrowthfactor
AT luozhuojing incorporationofchitosanmicrospheresintocollagenchitosanscaffoldsforthecontrolledreleaseofnervegrowthfactor