Evidence map›Paper›PMID 38799629›Full record

ArticleActa pharmaceutica Sinica. B2024

Metal natural product complex Ru-procyanidins with quadruple enzymatic activity combat infections from drug-resistant bacteria.

Jie Shan, Xu Jin, Cong Zhang, Muchen Huang, Jianghao Xing, Qingrong Li, Yuyu Cui, Qiang Niu, Xu Lin Chen, Xianwen Wang

Abstract read
In one paragraph

Article in Acta pharmaceutica Sinica. B, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

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  18. AuCu@CuOAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

10 authors.

Jie ShanDepartment of Burns, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Xu JinDepartment of Burns, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Cong ZhangDivision of Gastroenterology, the First Affiliated Hospital of USTC, Division of Life Science and Medicine, University of Science and Technology of China, Hefei, Anhui 230026, China.
Muchen HuangThe Second Clinical Medical College, Anhui Medical University, Hefei 230022, China.
Jianghao XingDepartment of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Qingrong LiSchool of Biomedical Engineering, Research and Engineering Center of Biomedical Materials, Anhui Provincial Institute of Translational Medicine, Anhui Medical University, Hefei 230032, China.
Yuyu CuiDepartment of Burns, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Qiang NiuThe Second Clinical Medical College, Anhui Medical University, Hefei 230022, China.
Xu Lin ChenDepartment of Burns, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Xianwen WangSchool of Biomedical Engineering, Research and Engineering Center of Biomedical Materials, Anhui Provincial Institute of Translational Medicine, Anhui Medical University, Hefei 230032, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial infection hampers wound repair by impeding the healing process. Concurrently, inflammation at the wound site triggers the production of reactive oxygen species (ROS), causing oxidative stress and damage to proteins and cells. This can lead to chronic wounds, posing severe risks. Therefore, eliminating bacterial infection and reducing ROS levels are crucial for effective wound healing. Nanozymes, possessing enzyme-like catalytic activity, can convert endogenous substances into highly toxic substances, such as ROS, to combat bacteria and biofilms without inducing drug resistance. However, the current nanozyme model with single enzyme activity falls short of meeting the complex requirements of antimicrobial therapy. Thus, developing nanozymes with multiple enzymatic activities is essential. Herein, we engineered a novel metalloenzyme called Ru-procyanidin nanoparticles (Ru-PC NPs) with diverse enzymatic activities to aid wound healing and combat bacterial infections. Under acidic conditions, due to their glutathione (GSH) depletion and peroxidase (POD)-like activity, Ru-PC NPs combined with H

Indexed as

Antibacterial therapyAnti-inflammatoryNanozymesQuadruple enzymatic activityReactive nitrogen speciesReactive oxygen speciesRNA-seqWound therapy

Identifiers

PMID38799629
PMCPMC11121202

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.