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3D-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking

3-dimensional (3D) bioprinting technology provides promising strategy in the fabrication of artificial tissues and organs. As the fundamental element in bioprinting process, preparation of bioink with ideal mechanical properties without sacrifice of biocompatibility is a great challenge. In this stu...

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Autores principales: Hu, Tian, Cui, Xiaoliang, Zhu, Meng, Wu, Man, Tian, Ye, Yao, Bin, Song, Wei, Niu, Zhongwei, Huang, Sha, Fu, Xiaobing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317699/
https://www.ncbi.nlm.nih.gov/pubmed/32637745
http://dx.doi.org/10.1016/j.bioactmat.2020.06.001
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author Hu, Tian
Cui, Xiaoliang
Zhu, Meng
Wu, Man
Tian, Ye
Yao, Bin
Song, Wei
Niu, Zhongwei
Huang, Sha
Fu, Xiaobing
author_facet Hu, Tian
Cui, Xiaoliang
Zhu, Meng
Wu, Man
Tian, Ye
Yao, Bin
Song, Wei
Niu, Zhongwei
Huang, Sha
Fu, Xiaobing
author_sort Hu, Tian
collection PubMed
description 3-dimensional (3D) bioprinting technology provides promising strategy in the fabrication of artificial tissues and organs. As the fundamental element in bioprinting process, preparation of bioink with ideal mechanical properties without sacrifice of biocompatibility is a great challenge. In this study, a supramolecular hydrogel-based bioink is prepared by polyethylene glycol (PEG) grafted chitosan, α-cyclodextrin (α-CD) and gelatin. It has a primary crosslinking structure through the aggregation of the pseudo-polyrotaxane-like side chains, which are formed from the host-guest interactions between α-CD and PEG side chain. Apparent viscosity measurement shows the shear-shinning property of this bioink, which might be due to the reversibility of the physical crosslinking. Moreover, with β-glycerophosphate at different concentrations as the secondary crosslinking agent, the printed constructs demonstrate different Young's modulus (p < 0.001). They could also maintain the Young's modulus in cell culture condition for at least 21 days (p < 0.05). By co-culturing each component with fibroblasts, CCK-8 assay demonstrate cellular viability is higher than 80%. After bioprinting and culturing, immunofluorescence staining with quantification indicate the expression of Ki-67, Paxillin, and N-cadherin is higher in day 14 than those in day 3 (p < 0.05). Oil red O and Nissl body specific staining reflect strength tunable bioink may have impact on the cell fate of mesenchymal stem cells (p < 0.05). This work might provide new idea for advanced bioink in the application of re-establishing complicated tissues and organs.
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spelling pubmed-73176992020-07-06 3D-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking Hu, Tian Cui, Xiaoliang Zhu, Meng Wu, Man Tian, Ye Yao, Bin Song, Wei Niu, Zhongwei Huang, Sha Fu, Xiaobing Bioact Mater Article 3-dimensional (3D) bioprinting technology provides promising strategy in the fabrication of artificial tissues and organs. As the fundamental element in bioprinting process, preparation of bioink with ideal mechanical properties without sacrifice of biocompatibility is a great challenge. In this study, a supramolecular hydrogel-based bioink is prepared by polyethylene glycol (PEG) grafted chitosan, α-cyclodextrin (α-CD) and gelatin. It has a primary crosslinking structure through the aggregation of the pseudo-polyrotaxane-like side chains, which are formed from the host-guest interactions between α-CD and PEG side chain. Apparent viscosity measurement shows the shear-shinning property of this bioink, which might be due to the reversibility of the physical crosslinking. Moreover, with β-glycerophosphate at different concentrations as the secondary crosslinking agent, the printed constructs demonstrate different Young's modulus (p < 0.001). They could also maintain the Young's modulus in cell culture condition for at least 21 days (p < 0.05). By co-culturing each component with fibroblasts, CCK-8 assay demonstrate cellular viability is higher than 80%. After bioprinting and culturing, immunofluorescence staining with quantification indicate the expression of Ki-67, Paxillin, and N-cadherin is higher in day 14 than those in day 3 (p < 0.05). Oil red O and Nissl body specific staining reflect strength tunable bioink may have impact on the cell fate of mesenchymal stem cells (p < 0.05). This work might provide new idea for advanced bioink in the application of re-establishing complicated tissues and organs. KeAi Publishing 2020-06-22 /pmc/articles/PMC7317699/ /pubmed/32637745 http://dx.doi.org/10.1016/j.bioactmat.2020.06.001 Text en © 2020 Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Hu, Tian
Cui, Xiaoliang
Zhu, Meng
Wu, Man
Tian, Ye
Yao, Bin
Song, Wei
Niu, Zhongwei
Huang, Sha
Fu, Xiaobing
3D-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking
title 3D-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking
title_full 3D-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking
title_fullStr 3D-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking
title_full_unstemmed 3D-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking
title_short 3D-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking
title_sort 3d-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317699/
https://www.ncbi.nlm.nih.gov/pubmed/32637745
http://dx.doi.org/10.1016/j.bioactmat.2020.06.001
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