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Non-invasive monitoring of in vivo hydrogel degradation and cartilage regeneration by multiparametric MR imaging
Numerous biodegradable hydrogels for cartilage regeneration have been widely used in the field of tissue engineering. However, to non-invasively monitor hydrogel degradation and efficiently evaluate cartilage restoration in situ is still challenging. Methods: A ultrasmall superparamagnetic iron oxid...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817116/ https://www.ncbi.nlm.nih.gov/pubmed/29464005 http://dx.doi.org/10.7150/thno.22514 |
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author | Chen, Zelong Yan, Chenggong Yan, Shina Liu, Qin Hou, Meirong Xu, Yikai Guo, Rui |
author_facet | Chen, Zelong Yan, Chenggong Yan, Shina Liu, Qin Hou, Meirong Xu, Yikai Guo, Rui |
author_sort | Chen, Zelong |
collection | PubMed |
description | Numerous biodegradable hydrogels for cartilage regeneration have been widely used in the field of tissue engineering. However, to non-invasively monitor hydrogel degradation and efficiently evaluate cartilage restoration in situ is still challenging. Methods: A ultrasmall superparamagnetic iron oxide (USPIO)-labeled cellulose nanocrystal (CNC)/silk fibroin (SF)-blended hydrogel system was developed to monitor hydrogel degradation during cartilage regeneration. The physicochemical characterization and biocompatibility of the hydrogel were evaluated in vitro. The in vivo hydrogel degradation and cartilage regeneration of different implants were assessed using multiparametric magnetic resonance imaging (MRI) and further confirmed by histological analysis in a rabbit cartilage defect model for 3 months. Results: USPIO-labeled hydrogels showed sufficient MR contrast enhancement and retained stability without loss of the relaxation rate. Neither the mechanical properties of the hydrogels nor the proliferation of bone-marrow mesenchymal stem cells (BMSCs) were affected by USPIO labeling in vitro. CNC/SF hydrogels with BMSCs degraded more quickly than the acellular hydrogels as reflected by the MR relaxation rate trends in vivo. The morphology of neocartilage was noninvasively visualized by the three-dimensional water-selective cartilage MRI scan sequence, and the cartilage repair was further demonstrated by macroscopic and histological observations. Conclusion: This USPIO-labeled CNC/SF hydrogel system provides a new perspective on image-guided tissue engineering for cartilage regeneration. |
format | Online Article Text |
id | pubmed-5817116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-58171162018-02-20 Non-invasive monitoring of in vivo hydrogel degradation and cartilage regeneration by multiparametric MR imaging Chen, Zelong Yan, Chenggong Yan, Shina Liu, Qin Hou, Meirong Xu, Yikai Guo, Rui Theranostics Research Paper Numerous biodegradable hydrogels for cartilage regeneration have been widely used in the field of tissue engineering. However, to non-invasively monitor hydrogel degradation and efficiently evaluate cartilage restoration in situ is still challenging. Methods: A ultrasmall superparamagnetic iron oxide (USPIO)-labeled cellulose nanocrystal (CNC)/silk fibroin (SF)-blended hydrogel system was developed to monitor hydrogel degradation during cartilage regeneration. The physicochemical characterization and biocompatibility of the hydrogel were evaluated in vitro. The in vivo hydrogel degradation and cartilage regeneration of different implants were assessed using multiparametric magnetic resonance imaging (MRI) and further confirmed by histological analysis in a rabbit cartilage defect model for 3 months. Results: USPIO-labeled hydrogels showed sufficient MR contrast enhancement and retained stability without loss of the relaxation rate. Neither the mechanical properties of the hydrogels nor the proliferation of bone-marrow mesenchymal stem cells (BMSCs) were affected by USPIO labeling in vitro. CNC/SF hydrogels with BMSCs degraded more quickly than the acellular hydrogels as reflected by the MR relaxation rate trends in vivo. The morphology of neocartilage was noninvasively visualized by the three-dimensional water-selective cartilage MRI scan sequence, and the cartilage repair was further demonstrated by macroscopic and histological observations. Conclusion: This USPIO-labeled CNC/SF hydrogel system provides a new perspective on image-guided tissue engineering for cartilage regeneration. Ivyspring International Publisher 2018-01-13 /pmc/articles/PMC5817116/ /pubmed/29464005 http://dx.doi.org/10.7150/thno.22514 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Chen, Zelong Yan, Chenggong Yan, Shina Liu, Qin Hou, Meirong Xu, Yikai Guo, Rui Non-invasive monitoring of in vivo hydrogel degradation and cartilage regeneration by multiparametric MR imaging |
title | Non-invasive monitoring of in vivo hydrogel degradation and cartilage regeneration by multiparametric MR imaging |
title_full | Non-invasive monitoring of in vivo hydrogel degradation and cartilage regeneration by multiparametric MR imaging |
title_fullStr | Non-invasive monitoring of in vivo hydrogel degradation and cartilage regeneration by multiparametric MR imaging |
title_full_unstemmed | Non-invasive monitoring of in vivo hydrogel degradation and cartilage regeneration by multiparametric MR imaging |
title_short | Non-invasive monitoring of in vivo hydrogel degradation and cartilage regeneration by multiparametric MR imaging |
title_sort | non-invasive monitoring of in vivo hydrogel degradation and cartilage regeneration by multiparametric mr imaging |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817116/ https://www.ncbi.nlm.nih.gov/pubmed/29464005 http://dx.doi.org/10.7150/thno.22514 |
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