Evidence map›Paper›PMID 42209494›Full record

ArticleNature communications2026

Self-adaptive nanozymes with enhanced multi-enzyme activities for sequential multimodal therapy of drug-resistant bacteria-infected wounds.

Xiaoyong Zhang, Hang Yu, Kai Zhu, Yao Xiao, Yuxuan Gong, Dandan Che, Wanyi Chen, Guoxing You, Xiyun Yan, Quan Wang and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

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

13 authors.

Xiaoyong ZhangAcademy of Military Medical Sciences, Beijing, China.ORCID http://orcid.org/0000-0003-1731-1887
Hang YuAcademy of Military Medical Sciences, Beijing, China.
Kai ZhuAcademy of Military Medical Sciences, Beijing, China.
Yao XiaoAcademy of Military Medical Sciences, Beijing, China.ORCID http://orcid.org/0009-0009-4567-9866
Yuxuan GongAcademy of Military Medical Sciences, Beijing, China.
Dandan CheAcademy of Military Medical Sciences, Beijing, China.
Wanyi ChenAcademy of Military Medical Sciences, Beijing, China.
Guoxing YouAcademy of Military Medical Sciences, Beijing, China.
Xiyun YanCAS Engineering Laboratory for Nanozyme, Key Laboratory of Biomacromolecules (CAS), CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.ORCID http://orcid.org/0000-0002-7290-352X
Quan WangAcademy of Military Medical Sciences, Beijing, China. wangquan0220@126.com.ORCID http://orcid.org/0009-0001-3298-2251
Kelong FanCAS Engineering Laboratory for Nanozyme, Key Laboratory of Biomacromolecules (CAS), CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China. fankelong@ibp.ac.cn.ORCID http://orcid.org/0000-0001-6285-1933
Hong ZhouAcademy of Military Medical Sciences, Beijing, China. zhouhtt1966@163.com.
Gan ChenAcademy of Military Medical Sciences, Beijing, China. chenlzu2005@163.com.ORCID http://orcid.org/0000-0003-4586-4526

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82572538National Natural Science Foundation of China (National Science Foundation of China) U23A20686
6 · The paper itself

Abstract

Drug-resistant bacterium-infected wounds pose a serious clinical challenge, underscoring the need for therapeutic materials that respond to dynamic healing stages. Herein, we report a sequential multimodal platform embedding a self-adaptive IrPtCu nanozyme into a madecassoside-enriched hyaluronic acid hydrogel (HIPCM) for rapid bacterial eradication and accelerated wound healing. Leveraging trimetallic synergy and pH-adaptive reactive oxygen species (ROS) regulation, IrPtCu nanozyme exhibits strong oxidase, peroxidase, glutathione oxidase, and glutathione peroxidase-like activities, enabling efficient ROS generation and potent antibacterial performance. After disinfection, it switches to ROS scavenging through superoxide dismutase and catalase-like cascades, alleviating oxidative stress and cooperating with madecassoside to promote tissue repair. In a methicillin-resistant Staphylococcus aureus (MRSA)-infected mouse model, HIPCM demonstrates strong antibacterial efficacy, promotes M2 macrophage polarization and angiogenesis, and accelerates high-quality repair. Preclinical studies in Bama mini-pigs further confirm improved collagen deposition, hair follicle regeneration, and functional restoration. This work offers a comprehensive strategy integrating adaptive nanozymes and natural herbal medicines for treating drug-resistant wounds.

Indexed as

Anti-Bacterial AgentsStaphylococcal InfectionsWound InfectionAnimalsCombined Modality TherapyDrug Resistance, BacterialHyaluronic AcidHydrogelsMethicillin-Resistant Staphylococcus aureusMiceOxidative StressReactive Oxygen SpeciesSwineSwine, MiniatureWound HealingAnti-Bacterial AgentsHyaluronic AcidHydrogelsReactive Oxygen Species

Identifiers

PMID42209494
PMCPMC13389173

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.