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Regulating Preparation Of Functional Alginate-Chitosan Three-Dimensional Scaffold For Skin Tissue Engineering

AIM: In this study, we attempted to regulate the preparation of Alg-CS-Flu three-dimensional scaffolds via a facile freeze-drying method combined with amidation. MATERIALS AND METHODS: Three-dimensional porous flurbiprofen-grafted alginate (Alg)–chitosan (CS) scaffolds were successfully prepared by...

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Autores principales: Zhu, Tonghe, Jiang, Jia, Zhao, Jinzhong, Chen, Sihao, Yan, Xiaoyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859126/
https://www.ncbi.nlm.nih.gov/pubmed/32009786
http://dx.doi.org/10.2147/IJN.S210329
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author Zhu, Tonghe
Jiang, Jia
Zhao, Jinzhong
Chen, Sihao
Yan, Xiaoyu
author_facet Zhu, Tonghe
Jiang, Jia
Zhao, Jinzhong
Chen, Sihao
Yan, Xiaoyu
author_sort Zhu, Tonghe
collection PubMed
description AIM: In this study, we attempted to regulate the preparation of Alg-CS-Flu three-dimensional scaffolds via a facile freeze-drying method combined with amidation. MATERIALS AND METHODS: Three-dimensional porous flurbiprofen-grafted alginate (Alg)–chitosan (CS) scaffolds were successfully prepared by a facile freeze-drying method combined with amidation for skin tissue engineering applications. Alg-CS composite was first used to load flurbiprofen (Flu), which is a kind of anti-inflammatory non-steroidal molecule. The Flu-loaded Alg/CS composite solution, through freeze-drying and 1-ethyl-3(3-(dimethylamino)propyl) carbodiimide/N-hydroxysuccinimide crosslinking to form an Alg-CS-Flu scaffold, exhibited a uniform and porous morphology that was characterized using scanning electron microscopy. The Alg-CS-Flu as-prepared scaffold was also characterized using Fourier-transform infrared spectroscopy, water contact angle, thermal properties, and stress-strain testing. RESULTS: The results reveal that Flu was successfully grafted onto the surfaces of the Alg-CS-Flu scaffold, which showed good hydrophilicity and appropriate mechanical properties. Furthermore, cell viability, cell morphology from cells cultured in vitro, and hematoxylin-eosin staining after the graft was subcutaneously embedded in mice for 7 d demonstrated that the Alg-CS-Flu scaffold had no unfavorable effects on the adhesion and proliferation of fibroblasts, as well as a good anti-inflammatory property. CONCLUSION: The developed Alg-CS-Flu scaffold is proposed as a promising material or skin tissue engineering application.
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spelling pubmed-68591262020-01-31 Regulating Preparation Of Functional Alginate-Chitosan Three-Dimensional Scaffold For Skin Tissue Engineering Zhu, Tonghe Jiang, Jia Zhao, Jinzhong Chen, Sihao Yan, Xiaoyu Int J Nanomedicine Original Research AIM: In this study, we attempted to regulate the preparation of Alg-CS-Flu three-dimensional scaffolds via a facile freeze-drying method combined with amidation. MATERIALS AND METHODS: Three-dimensional porous flurbiprofen-grafted alginate (Alg)–chitosan (CS) scaffolds were successfully prepared by a facile freeze-drying method combined with amidation for skin tissue engineering applications. Alg-CS composite was first used to load flurbiprofen (Flu), which is a kind of anti-inflammatory non-steroidal molecule. The Flu-loaded Alg/CS composite solution, through freeze-drying and 1-ethyl-3(3-(dimethylamino)propyl) carbodiimide/N-hydroxysuccinimide crosslinking to form an Alg-CS-Flu scaffold, exhibited a uniform and porous morphology that was characterized using scanning electron microscopy. The Alg-CS-Flu as-prepared scaffold was also characterized using Fourier-transform infrared spectroscopy, water contact angle, thermal properties, and stress-strain testing. RESULTS: The results reveal that Flu was successfully grafted onto the surfaces of the Alg-CS-Flu scaffold, which showed good hydrophilicity and appropriate mechanical properties. Furthermore, cell viability, cell morphology from cells cultured in vitro, and hematoxylin-eosin staining after the graft was subcutaneously embedded in mice for 7 d demonstrated that the Alg-CS-Flu scaffold had no unfavorable effects on the adhesion and proliferation of fibroblasts, as well as a good anti-inflammatory property. CONCLUSION: The developed Alg-CS-Flu scaffold is proposed as a promising material or skin tissue engineering application. Dove 2019-11-13 /pmc/articles/PMC6859126/ /pubmed/32009786 http://dx.doi.org/10.2147/IJN.S210329 Text en © 2019 Zhu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zhu, Tonghe
Jiang, Jia
Zhao, Jinzhong
Chen, Sihao
Yan, Xiaoyu
Regulating Preparation Of Functional Alginate-Chitosan Three-Dimensional Scaffold For Skin Tissue Engineering
title Regulating Preparation Of Functional Alginate-Chitosan Three-Dimensional Scaffold For Skin Tissue Engineering
title_full Regulating Preparation Of Functional Alginate-Chitosan Three-Dimensional Scaffold For Skin Tissue Engineering
title_fullStr Regulating Preparation Of Functional Alginate-Chitosan Three-Dimensional Scaffold For Skin Tissue Engineering
title_full_unstemmed Regulating Preparation Of Functional Alginate-Chitosan Three-Dimensional Scaffold For Skin Tissue Engineering
title_short Regulating Preparation Of Functional Alginate-Chitosan Three-Dimensional Scaffold For Skin Tissue Engineering
title_sort regulating preparation of functional alginate-chitosan three-dimensional scaffold for skin tissue engineering
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859126/
https://www.ncbi.nlm.nih.gov/pubmed/32009786
http://dx.doi.org/10.2147/IJN.S210329
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