Evidence map›Paper›PMID 42436805›Full record

ArticleMaterials today. Bio2026

Mechanoregulative hydrogel enables scar-reduced and functional healing of infected diabetic mobile wounds.

Jiakang Zhang, Yuanru Lang, Yuhui Zhang, Qian Liu, Long Chen, Hongli Jin, Yuntong Zhang, Shuo Fang

Abstract read
In one paragraph

Article in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jiakang ZhangShanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, PR China.
Yuanru LangInstitute of Molecular Medicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, PR China.
Yuhui ZhangShanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, PR China.
Qian LiuShanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, PR China.
Long ChenShanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, PR China.
Hongli JinShanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, PR China.
Yuntong ZhangDepartment of Trauma and Orthopedic Surgery, The First Affiliated Hospital of Navy Medical University, Shanghai, 200433, PR China.
Shuo FangDepartment of Plastic Surgery, The First Affiliated Hospital of Navy Medical University, Shanghai, 200433, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic infected wounds at mobile sites are characterized by persistent hyperglycemia, oxidative stress, and drug-resistant bacterial colonization, which collectively establish a self-amplifying infection-inflammation cycle. Meanwhile, wounds located at mechanically active regions, such as the nape and joints, are continuously exposed to stretching and repetitive deformation, leading to heterogeneous stress distribution at the wound edge, fibrotic remodeling, and hypertrophic scar formation. Therefore, simultaneous regulation of biochemical pathology and mechanical imbalance is essential for high-quality healing of diabetic mobile wounds. Here, we develop a multilevel mechanoregulative hydrogel to coordinately regulate the bio-mechanical microenvironment of diabetic infected wounds at mobile sites. The inner dynamic boronate ester network functions as a glucose-responsive delivery platform for on-demand release of polyhexamethylene biguanide (PHMB) and oxidative stress-balancing OPC-Ce nanoparticles (OPC-Ce NPs), enabling efficient eradication of drug-resistant bacteria, ROS scavenging, and inflammatory microenvironment remodeling. The outer elastic network absorbs, disperses, and homogenizes wound-edge forces to reconfigure local stress distribution, thereby suppressing fibrosis activation in high-stress regions while improving impaired cellular activity in low-stress regions. In addition, the outer layer recaptures excess PHMB, reducing cytotoxicity associated with prolonged antibacterial exposure. In vivo, this hydrogel markedly promotes ordered regeneration of diabetic mobile wounds, as evidenced by normalized epidermal differentiation, enhanced hair follicle neogenesis, restrained dermal fibroblast overactivation, and functional remodeling of neovasculature and extracellular matrix. This study establishes a therapeutic strategy that integrates anti-infective/anti-inflammatory regulation, dynamic antibacterial agent management, and mechanical stress regulation, offering a new materials paradigm for scar-reduced repair of infected diabetic wounds on mobile joints.

Indexed as

Controlled release and recapture behaviorInfected diabetic mobile woundsMechanical force regulationMechanical homeostasis

Identifiers

PMID42436805
PMCPMC13355570

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.