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Fabrication of gelatin-based and Zn(2+)-incorporated composite hydrogel for accelerated infected wound healing

Gelatin-based hydrogels have a broad range of biomedical fields due to their biocompatibility, convenience for chemical modifications, and degradability. However, gelatin-based hydrogels present poor antibacterial ability that hinders their applications in treating infected wound healing. Herein, a...

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Autores principales: Tao, Bailong, Lin, Chuanchuan, Qin, Xian, Yu, Yonglin, Guo, Ai, Li, Kai, Tian, Hongchuan, Yi, Weiwei, Lei, Dengliang, Chen, Yue, Chen, Lixue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857474/
https://www.ncbi.nlm.nih.gov/pubmed/35243291
http://dx.doi.org/10.1016/j.mtbio.2022.100216
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author Tao, Bailong
Lin, Chuanchuan
Qin, Xian
Yu, Yonglin
Guo, Ai
Li, Kai
Tian, Hongchuan
Yi, Weiwei
Lei, Dengliang
Chen, Yue
Chen, Lixue
author_facet Tao, Bailong
Lin, Chuanchuan
Qin, Xian
Yu, Yonglin
Guo, Ai
Li, Kai
Tian, Hongchuan
Yi, Weiwei
Lei, Dengliang
Chen, Yue
Chen, Lixue
author_sort Tao, Bailong
collection PubMed
description Gelatin-based hydrogels have a broad range of biomedical fields due to their biocompatibility, convenience for chemical modifications, and degradability. However, gelatin-based hydrogels present poor antibacterial ability that hinders their applications in treating infected wound healing. Herein, a series of multifunctional hydrogels (Gel@Zn) were fabricated through free-radical polymerization interaction based on gelatin methacrylate (GelMA) and dopamine methacrylate (DMA), and then immersed them into zinc nitrate solutions based on the metal coordination and ionic bonding interaction. These designed hydrogels wound dressings show strong antibacterial activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) by increasing intracellular reactive oxygen species (ROS) level and changing bacterial membrane permeability. Meanwhile, the hydrogels exhibit good cytocompatibility, enhance the adhesion, proliferation, and migration of NIH-3T3 cells. Furthermore, Gel@Zn-0.08 (0.08 ​M Zn(2+) immersed with Gel sample) presents a good balance between antibacterial effect, cell viability, and hemolytic property. Compared with 3 ​M commercial dressings, Gel@Zn-0.04, and Gel@Zn-0.16, the Gel@Zn-0.08 could significantly improve the healing process of S. aureus-infected full-thickness wounds via restrained the inflammatory responses, enhanced epidermis and granulation tissue information, and stimulated angiogenesis. Our study indicates that the Zn-incorporated hydrogels are promising bioactive materials as wound dressings for infected full-thickness wound healing and skin regeneration.
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spelling pubmed-88574742022-03-02 Fabrication of gelatin-based and Zn(2+)-incorporated composite hydrogel for accelerated infected wound healing Tao, Bailong Lin, Chuanchuan Qin, Xian Yu, Yonglin Guo, Ai Li, Kai Tian, Hongchuan Yi, Weiwei Lei, Dengliang Chen, Yue Chen, Lixue Mater Today Bio Full Length Article Gelatin-based hydrogels have a broad range of biomedical fields due to their biocompatibility, convenience for chemical modifications, and degradability. However, gelatin-based hydrogels present poor antibacterial ability that hinders their applications in treating infected wound healing. Herein, a series of multifunctional hydrogels (Gel@Zn) were fabricated through free-radical polymerization interaction based on gelatin methacrylate (GelMA) and dopamine methacrylate (DMA), and then immersed them into zinc nitrate solutions based on the metal coordination and ionic bonding interaction. These designed hydrogels wound dressings show strong antibacterial activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) by increasing intracellular reactive oxygen species (ROS) level and changing bacterial membrane permeability. Meanwhile, the hydrogels exhibit good cytocompatibility, enhance the adhesion, proliferation, and migration of NIH-3T3 cells. Furthermore, Gel@Zn-0.08 (0.08 ​M Zn(2+) immersed with Gel sample) presents a good balance between antibacterial effect, cell viability, and hemolytic property. Compared with 3 ​M commercial dressings, Gel@Zn-0.04, and Gel@Zn-0.16, the Gel@Zn-0.08 could significantly improve the healing process of S. aureus-infected full-thickness wounds via restrained the inflammatory responses, enhanced epidermis and granulation tissue information, and stimulated angiogenesis. Our study indicates that the Zn-incorporated hydrogels are promising bioactive materials as wound dressings for infected full-thickness wound healing and skin regeneration. Elsevier 2022-02-09 /pmc/articles/PMC8857474/ /pubmed/35243291 http://dx.doi.org/10.1016/j.mtbio.2022.100216 Text en © 2022 The Authors 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 Full Length Article
Tao, Bailong
Lin, Chuanchuan
Qin, Xian
Yu, Yonglin
Guo, Ai
Li, Kai
Tian, Hongchuan
Yi, Weiwei
Lei, Dengliang
Chen, Yue
Chen, Lixue
Fabrication of gelatin-based and Zn(2+)-incorporated composite hydrogel for accelerated infected wound healing
title Fabrication of gelatin-based and Zn(2+)-incorporated composite hydrogel for accelerated infected wound healing
title_full Fabrication of gelatin-based and Zn(2+)-incorporated composite hydrogel for accelerated infected wound healing
title_fullStr Fabrication of gelatin-based and Zn(2+)-incorporated composite hydrogel for accelerated infected wound healing
title_full_unstemmed Fabrication of gelatin-based and Zn(2+)-incorporated composite hydrogel for accelerated infected wound healing
title_short Fabrication of gelatin-based and Zn(2+)-incorporated composite hydrogel for accelerated infected wound healing
title_sort fabrication of gelatin-based and zn(2+)-incorporated composite hydrogel for accelerated infected wound healing
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857474/
https://www.ncbi.nlm.nih.gov/pubmed/35243291
http://dx.doi.org/10.1016/j.mtbio.2022.100216
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