Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/174714
Title: Hydrogel dressings with intrinsic antibiofilm and antioxidative dual functionalities accelerate infected diabetic wound healing
Authors: Pranantyo, Dicky
Yeo, Chun Kiat
Wu, Yang
Fan, Chen
Xu, Xiaofei
Yip, Yun Sheng
Vos, Marcus Ivan Gerard
Mahadevegowda, Surendra H.
Lim, Priscilla Lay Keng
Yang, Liang
Hammond, Paula T.
Leavesley, David Ian
Tan, Nguan Soon
Chan-Park, Mary B.
Keywords: Medicine, Health and Life Sciences
Issue Date: 2024
Source: Pranantyo, D., Yeo, C. K., Wu, Y., Fan, C., Xu, X., Yip, Y. S., Vos, M. I. G., Mahadevegowda, S. H., Lim, P. L. K., Yang, L., Hammond, P. T., Leavesley, D. I., Tan, N. S. & Chan-Park, M. B. (2024). Hydrogel dressings with intrinsic antibiofilm and antioxidative dual functionalities accelerate infected diabetic wound healing. Nature Communications, 15(1), 954-. https://dx.doi.org/10.1038/s41467-024-44968-y
Project: H17/01/a0/0B9 
H17/01/a0/0M9 
H19/01/a0/OY9 
H17/ 01/a0/009 
MOE2018-T3-1-003 
Journal: Nature Communications 
Abstract: Chronic wounds are often infected with biofilm bacteria and characterized by high oxidative stress. Current dressings that promote chronic wound healing either require additional processes such as photothermal irradiation or leave behind gross amounts of undesirable residues. We report a dual-functionality hydrogel dressing with intrinsic antibiofilm and antioxidative properties that are synergistic and low-leaching. The hydrogel is a crosslinked network with tethered antibacterial cationic polyimidazolium and antioxidative N-acetylcysteine. In a murine diabetic wound model, the hydrogel accelerates the closure of wounds infected with methicillin-resistant Staphylococcus aureus or carbapenem-resistant Pseudomonas aeruginosa biofilm. Furthermore, a three-dimensional ex vivo human skin equivalent model shows that N-acetylcysteine promotes the keratinocyte differentiation and accelerates the re-epithelialization process. Our hydrogel dressing can be made into different formats for the healing of both flat and deep infected chronic wounds without contamination of the wound or needing other modalities such as photothermal irradiation.
URI: https://hdl.handle.net/10356/174714
ISSN: 2041-1723
DOI: 10.1038/s41467-024-44968-y
Schools: School of Chemistry, Chemical Engineering and Biotechnology 
Interdisciplinary Graduate School (IGS) 
Lee Kong Chian School of Medicine (LKCMedicine) 
School of Biological Sciences 
Organisations: Singapore-MIT Alliance for Research and Technology 
Research Centres: Centre for Antimicrobial Bioengineering
NTU Institute for Health Technologies
Rights: © The Author(s) 2024. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/ licenses/by/4.0/.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:CCEB Journal Articles

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