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Co-delivery of VEGF and bFGF via a PLGA nanoparticle-modified BAM for effective contracture inhibition of regenerated bladder tissue in rabbits

Graft contracture is a common problem associated with the regeneration processes of tissue-engineered bladders. Currently, most strategies used for incorporating bioactive molecules into biomaterial designs do not work during all phases of tissue regeneration. In this study, we used a growth factor-...

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Autores principales: Jiang, Xincheng, Lin, Houwei, Jiang, Dapeng, Xu, Guofeng, Fang, Xiaoliang, He, Lei, Xu, Maosheng, Tang, Bingqiang, Wang, Zhiyong, Cui, Daxiang, Chen, Fang, Geng, Hongquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745101/
https://www.ncbi.nlm.nih.gov/pubmed/26854200
http://dx.doi.org/10.1038/srep20784
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author Jiang, Xincheng
Lin, Houwei
Jiang, Dapeng
Xu, Guofeng
Fang, Xiaoliang
He, Lei
Xu, Maosheng
Tang, Bingqiang
Wang, Zhiyong
Cui, Daxiang
Chen, Fang
Geng, Hongquan
author_facet Jiang, Xincheng
Lin, Houwei
Jiang, Dapeng
Xu, Guofeng
Fang, Xiaoliang
He, Lei
Xu, Maosheng
Tang, Bingqiang
Wang, Zhiyong
Cui, Daxiang
Chen, Fang
Geng, Hongquan
author_sort Jiang, Xincheng
collection PubMed
description Graft contracture is a common problem associated with the regeneration processes of tissue-engineered bladders. Currently, most strategies used for incorporating bioactive molecules into biomaterial designs do not work during all phases of tissue regeneration. In this study, we used a growth factor-PLGA nanoparticle thermo-sensitive gel system (i.e., BAM with incorporated VEGF and bFGF-loaded PLGA nanoparticles and mixed with a hydrophilic gel) to promote bladder tissue regeneration in a rabbit model. At 4 and 12 weeks after surgery, contracture rate assessment and histological examination were conducted to evaluate bladder tissue regeneration. The results indicated that the functional composite scaffold continuously and effectively released VEGF and bFGF and promoted bladder reconstruction with a significant decrease in graft contracture. In addition, the number and arrangement of regenerated urothelial cells and smooth muscle cells as well as microvascular density and maturity were improved in the VEGF/bFGF nanoparticle group compared with the single factor VEGF or bFGF nanoparticle group and BAM alone. The nanoparticle thermo-sensitive gel system, which exhibited favourable performance, may effectively inhibit graft contracture and promote bladder tissue regeneration in rabbits.
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spelling pubmed-47451012016-02-16 Co-delivery of VEGF and bFGF via a PLGA nanoparticle-modified BAM for effective contracture inhibition of regenerated bladder tissue in rabbits Jiang, Xincheng Lin, Houwei Jiang, Dapeng Xu, Guofeng Fang, Xiaoliang He, Lei Xu, Maosheng Tang, Bingqiang Wang, Zhiyong Cui, Daxiang Chen, Fang Geng, Hongquan Sci Rep Article Graft contracture is a common problem associated with the regeneration processes of tissue-engineered bladders. Currently, most strategies used for incorporating bioactive molecules into biomaterial designs do not work during all phases of tissue regeneration. In this study, we used a growth factor-PLGA nanoparticle thermo-sensitive gel system (i.e., BAM with incorporated VEGF and bFGF-loaded PLGA nanoparticles and mixed with a hydrophilic gel) to promote bladder tissue regeneration in a rabbit model. At 4 and 12 weeks after surgery, contracture rate assessment and histological examination were conducted to evaluate bladder tissue regeneration. The results indicated that the functional composite scaffold continuously and effectively released VEGF and bFGF and promoted bladder reconstruction with a significant decrease in graft contracture. In addition, the number and arrangement of regenerated urothelial cells and smooth muscle cells as well as microvascular density and maturity were improved in the VEGF/bFGF nanoparticle group compared with the single factor VEGF or bFGF nanoparticle group and BAM alone. The nanoparticle thermo-sensitive gel system, which exhibited favourable performance, may effectively inhibit graft contracture and promote bladder tissue regeneration in rabbits. Nature Publishing Group 2016-02-08 /pmc/articles/PMC4745101/ /pubmed/26854200 http://dx.doi.org/10.1038/srep20784 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Jiang, Xincheng
Lin, Houwei
Jiang, Dapeng
Xu, Guofeng
Fang, Xiaoliang
He, Lei
Xu, Maosheng
Tang, Bingqiang
Wang, Zhiyong
Cui, Daxiang
Chen, Fang
Geng, Hongquan
Co-delivery of VEGF and bFGF via a PLGA nanoparticle-modified BAM for effective contracture inhibition of regenerated bladder tissue in rabbits
title Co-delivery of VEGF and bFGF via a PLGA nanoparticle-modified BAM for effective contracture inhibition of regenerated bladder tissue in rabbits
title_full Co-delivery of VEGF and bFGF via a PLGA nanoparticle-modified BAM for effective contracture inhibition of regenerated bladder tissue in rabbits
title_fullStr Co-delivery of VEGF and bFGF via a PLGA nanoparticle-modified BAM for effective contracture inhibition of regenerated bladder tissue in rabbits
title_full_unstemmed Co-delivery of VEGF and bFGF via a PLGA nanoparticle-modified BAM for effective contracture inhibition of regenerated bladder tissue in rabbits
title_short Co-delivery of VEGF and bFGF via a PLGA nanoparticle-modified BAM for effective contracture inhibition of regenerated bladder tissue in rabbits
title_sort co-delivery of vegf and bfgf via a plga nanoparticle-modified bam for effective contracture inhibition of regenerated bladder tissue in rabbits
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745101/
https://www.ncbi.nlm.nih.gov/pubmed/26854200
http://dx.doi.org/10.1038/srep20784
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