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Enzyme-mediated one-pot synthesis of hydrogel with the polyphenol cross-linker for skin regeneration
Polyphenols can trigger immunity that activates intracellular anti-inflammatory signaling and prevents external infections. In this study, we report the fabrication of chitosan-based hydrogels with epigallocatechin gallate (EGCG) using enzyme-mediated one-pot synthesis. The tyrosinase-mediated oxida...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575804/ https://www.ncbi.nlm.nih.gov/pubmed/33103105 http://dx.doi.org/10.1016/j.mtbio.2020.100079 |
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author | Kim, B.S. Kim, S.-H. Kim, K. An, Y.-H. So, K.-H. Kim, B.-G. Hwang, N.S. |
author_facet | Kim, B.S. Kim, S.-H. Kim, K. An, Y.-H. So, K.-H. Kim, B.-G. Hwang, N.S. |
author_sort | Kim, B.S. |
collection | PubMed |
description | Polyphenols can trigger immunity that activates intracellular anti-inflammatory signaling and prevents external infections. In this study, we report the fabrication of chitosan-based hydrogels with epigallocatechin gallate (EGCG) using enzyme-mediated one-pot synthesis. The tyrosinase-mediated oxidative reaction of the phenolic rings of EGCG with the primary amines on chitosan results in stable EGCG-chitosan hydrogels. The EGCG concentrations contributed to the cross-linking density and physical properties of EGCG-chitosan hydrogels. Furthermore, EGCG-chitosan hydrogels maintained intrinsic properties such as antibacterial and antioxidant effects. When endotoxin-activated RAW 264.7 macrophage cells were cultured with EGCG-chitosan hydrogels, the hydrogels reduced the inflammatory response of the RAW 264.7 cells. Furthermore, subcutaneous implantation of EGCG-chitosan hydrogels reduced endogenous macrophage and monocyte activation. When the EGCG-chitosan hydrogels were applied to a full-skin defect wound, they facilitated skin regeneration. Our study demonstrates that the one-pot synthesized EGCG-chitosan hydrogels can be applied in broad tissue regeneration applications that require immune modulation. |
format | Online Article Text |
id | pubmed-7575804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75758042020-10-23 Enzyme-mediated one-pot synthesis of hydrogel with the polyphenol cross-linker for skin regeneration Kim, B.S. Kim, S.-H. Kim, K. An, Y.-H. So, K.-H. Kim, B.-G. Hwang, N.S. Mater Today Bio Full Length Article Polyphenols can trigger immunity that activates intracellular anti-inflammatory signaling and prevents external infections. In this study, we report the fabrication of chitosan-based hydrogels with epigallocatechin gallate (EGCG) using enzyme-mediated one-pot synthesis. The tyrosinase-mediated oxidative reaction of the phenolic rings of EGCG with the primary amines on chitosan results in stable EGCG-chitosan hydrogels. The EGCG concentrations contributed to the cross-linking density and physical properties of EGCG-chitosan hydrogels. Furthermore, EGCG-chitosan hydrogels maintained intrinsic properties such as antibacterial and antioxidant effects. When endotoxin-activated RAW 264.7 macrophage cells were cultured with EGCG-chitosan hydrogels, the hydrogels reduced the inflammatory response of the RAW 264.7 cells. Furthermore, subcutaneous implantation of EGCG-chitosan hydrogels reduced endogenous macrophage and monocyte activation. When the EGCG-chitosan hydrogels were applied to a full-skin defect wound, they facilitated skin regeneration. Our study demonstrates that the one-pot synthesized EGCG-chitosan hydrogels can be applied in broad tissue regeneration applications that require immune modulation. Elsevier 2020-09-21 /pmc/articles/PMC7575804/ /pubmed/33103105 http://dx.doi.org/10.1016/j.mtbio.2020.100079 Text en © 2020 The Authors http://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 Kim, B.S. Kim, S.-H. Kim, K. An, Y.-H. So, K.-H. Kim, B.-G. Hwang, N.S. Enzyme-mediated one-pot synthesis of hydrogel with the polyphenol cross-linker for skin regeneration |
title | Enzyme-mediated one-pot synthesis of hydrogel with the polyphenol cross-linker for skin regeneration |
title_full | Enzyme-mediated one-pot synthesis of hydrogel with the polyphenol cross-linker for skin regeneration |
title_fullStr | Enzyme-mediated one-pot synthesis of hydrogel with the polyphenol cross-linker for skin regeneration |
title_full_unstemmed | Enzyme-mediated one-pot synthesis of hydrogel with the polyphenol cross-linker for skin regeneration |
title_short | Enzyme-mediated one-pot synthesis of hydrogel with the polyphenol cross-linker for skin regeneration |
title_sort | enzyme-mediated one-pot synthesis of hydrogel with the polyphenol cross-linker for skin regeneration |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575804/ https://www.ncbi.nlm.nih.gov/pubmed/33103105 http://dx.doi.org/10.1016/j.mtbio.2020.100079 |
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