AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (11.7 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Research Article | Open Access

Multifunctional nanoparticle-reinforced tissue-derived hydrogel for accelerated healing of drug-resistant Pseudomonas aeruginosa infected wounds

Jialu Lang1,2,3,§Chunlei Shan1,§Yuanzhi Ju2Qi Zhu3Jiawen Zhu3Xiaochuan Wu3Jiahao Hu3Yuanyan Huang3Di Chen2Gang Han1 ( )Yongzhong Du2,3 ( )Zhenwei Yu1,2 ( )
Department of Pharmacy, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou 310016, China
Research Center for Clinical Pharmacy, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China
State Key Laboratory of Advanced Drug Delivery and Release Systems, Institute of Pharmaceutics, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China

§ Jialu Lang and Chunlei Shan contributed equally to this work.

Show Author Information

Abstract

Chronic wounds complicated by multidrug-resistant bacterial infections pose a serious therapeutic challenge. Here, we develop a multifunctional hydrogel (PmB/Ag-PDA@ECM) by integrating silver nanoparticle-modified polydopamine (Ag-PDA) and polymyxin B (PmB) into a thermosensitive, pro-regenerative extracellular matrix (ECM) hydrogel. The hydrogel exhibits favorable physicochemical properties, including a porous microstructure (49.24% porosity), rapid swelling (~ 1068%), and strong tissue adhesion (6.24 kPa). Upon near-infrared (NIR) irradiation, it achieves mild photothermal heating (~ 50 °C), triggering synergistic antibacterial effects that completely eradicate polymyxin B-resistant Pseudomonas aeruginosa (PRPA). In vitro, the hydrogel promotes keratinocyte and endothelial cell proliferation and migration, while maintaining excellent cytocompatibility and hemocompatibility. In a PRPA-infected full-thickness wound model, the hydrogel rapidly sterilizes the wound bed and accelerates wound closure. Moreover, it effectively suppresses inflammation (reduced tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6)), promotes M2 macrophage polarization, and facilitates tissue remodeling, including neovascularization and regeneration of skin appendages. This work presents a clinically translatable hydrogel platform that simultaneously addresses antimicrobial resistance and supports high-quality tissue regeneration, offering a promising strategy for the treatment of complex infected wounds.

Graphical Abstract

This study developed a multifunctional PmB/Ag-PDA@ECM hydrogel that combines silver nanoparticle-modified polydopamine and polymyxin B to eradicate drug-resistant Pseudomonas aeruginosa through photothermal and chemical therapy.

Electronic Supplementary Material

Download File(s)
8546_ESM.pdf (1.3 MB)

References

【1】
【1】
 
 
Nano Research
Article number: 94908546

{{item.num}}

Comments on this article

Go to comment

< Back to all reports

Review Status: {{reviewData.commendedNum}} Commended , {{reviewData.revisionRequiredNum}} Revision Required , {{reviewData.notCommendedNum}} Not Commended Under Peer Review

Review Comment

Close
Close
Cite this article:
Lang J, Shan C, Ju Y, et al. Multifunctional nanoparticle-reinforced tissue-derived hydrogel for accelerated healing of drug-resistant Pseudomonas aeruginosa infected wounds. Nano Research, 2026, 19(6): 94908546. https://doi.org/10.26599/NR.2026.94908546
Topics:

831

Views

119

Downloads

0

Crossref

0

Web of Science

0

Scopus

0

CSCD

Received: 18 December 2025
Revised: 04 February 2026
Accepted: 06 February 2026
Published: 29 April 2026
© The Author(s) 2026. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).