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Bioactive skin-mimicking hydrogel band-aids for diabetic wound healing and infectious skin incision treatment
The treatment of diabetic chronic wounds remains a global challenge due to the up-regulated inflammation response, oxidant stress, and persistent infection during healing process. Developing wound dressing materials with ideal biocompatibility, adequate mechanical strength, considerable under-water...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079829/ https://www.ncbi.nlm.nih.gov/pubmed/33937595 http://dx.doi.org/10.1016/j.bioactmat.2021.04.007 |
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author | Yang, Yuxuan Zhao, Xiaodan Yu, Jing Chen, Xingxing Wang, Ruyue Zhang, Mengyuan Zhang, Qiang Zhang, Yanfeng Wang, Shuang Cheng, Yilong |
author_facet | Yang, Yuxuan Zhao, Xiaodan Yu, Jing Chen, Xingxing Wang, Ruyue Zhang, Mengyuan Zhang, Qiang Zhang, Yanfeng Wang, Shuang Cheng, Yilong |
author_sort | Yang, Yuxuan |
collection | PubMed |
description | The treatment of diabetic chronic wounds remains a global challenge due to the up-regulated inflammation response, oxidant stress, and persistent infection during healing process. Developing wound dressing materials with ideal biocompatibility, adequate mechanical strength, considerable under-water adhesion, sufficient anti-inflammation, antioxidant, and antibacterial properties is on-demand for clinical applications. In this study, we developed a bioactive skin-mimicking hydrogel band-aid through the combination of tannic acid (TA) and imidazolidinyl urea reinforced polyurethane (PMI) (TAP hydrogel) and explored its potentials in various medical applications, including hemostasis, normal skin incision, full-thickness skin wounds, and bacterial-infection skin incision on diabetic mice. TA was loaded into PMI hydrogel network to enhance the mechanical properties of TAP hydrogels through multiple non-covalent interactions (break strength: 0.28–0.64 MPa; elongation at break: 650–930%), which could resist the local stress and maintain the structural integrity of wound dressings during applications. Moreover, owing to the promising moisture-resistant adhesiveness and organ hemostasis, outstanding anti-inflammation, antibacterial, and antioxidant properties, TAP hydrogels could efficiently promote the recovery of skin incision and defects on diabetic mice. To further simulate the practical situation and explore the potential in clinical application, we also verified the treatment efficiency of TAP hydrogel in S. aureus-infected skin incision model on diabetic mice. |
format | Online Article Text |
id | pubmed-8079829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-80798292021-04-30 Bioactive skin-mimicking hydrogel band-aids for diabetic wound healing and infectious skin incision treatment Yang, Yuxuan Zhao, Xiaodan Yu, Jing Chen, Xingxing Wang, Ruyue Zhang, Mengyuan Zhang, Qiang Zhang, Yanfeng Wang, Shuang Cheng, Yilong Bioact Mater Article The treatment of diabetic chronic wounds remains a global challenge due to the up-regulated inflammation response, oxidant stress, and persistent infection during healing process. Developing wound dressing materials with ideal biocompatibility, adequate mechanical strength, considerable under-water adhesion, sufficient anti-inflammation, antioxidant, and antibacterial properties is on-demand for clinical applications. In this study, we developed a bioactive skin-mimicking hydrogel band-aid through the combination of tannic acid (TA) and imidazolidinyl urea reinforced polyurethane (PMI) (TAP hydrogel) and explored its potentials in various medical applications, including hemostasis, normal skin incision, full-thickness skin wounds, and bacterial-infection skin incision on diabetic mice. TA was loaded into PMI hydrogel network to enhance the mechanical properties of TAP hydrogels through multiple non-covalent interactions (break strength: 0.28–0.64 MPa; elongation at break: 650–930%), which could resist the local stress and maintain the structural integrity of wound dressings during applications. Moreover, owing to the promising moisture-resistant adhesiveness and organ hemostasis, outstanding anti-inflammation, antibacterial, and antioxidant properties, TAP hydrogels could efficiently promote the recovery of skin incision and defects on diabetic mice. To further simulate the practical situation and explore the potential in clinical application, we also verified the treatment efficiency of TAP hydrogel in S. aureus-infected skin incision model on diabetic mice. KeAi Publishing 2021-04-17 /pmc/articles/PMC8079829/ /pubmed/33937595 http://dx.doi.org/10.1016/j.bioactmat.2021.04.007 Text en © 2021 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 | Article Yang, Yuxuan Zhao, Xiaodan Yu, Jing Chen, Xingxing Wang, Ruyue Zhang, Mengyuan Zhang, Qiang Zhang, Yanfeng Wang, Shuang Cheng, Yilong Bioactive skin-mimicking hydrogel band-aids for diabetic wound healing and infectious skin incision treatment |
title | Bioactive skin-mimicking hydrogel band-aids for diabetic wound healing and infectious skin incision treatment |
title_full | Bioactive skin-mimicking hydrogel band-aids for diabetic wound healing and infectious skin incision treatment |
title_fullStr | Bioactive skin-mimicking hydrogel band-aids for diabetic wound healing and infectious skin incision treatment |
title_full_unstemmed | Bioactive skin-mimicking hydrogel band-aids for diabetic wound healing and infectious skin incision treatment |
title_short | Bioactive skin-mimicking hydrogel band-aids for diabetic wound healing and infectious skin incision treatment |
title_sort | bioactive skin-mimicking hydrogel band-aids for diabetic wound healing and infectious skin incision treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079829/ https://www.ncbi.nlm.nih.gov/pubmed/33937595 http://dx.doi.org/10.1016/j.bioactmat.2021.04.007 |
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