Evidence map›Paper›PMID 40755466›Full record

ReviewInternational journal of nanomedicine2025

Recent Advances in Nanozymes for the Treatment of Atherosclerosis.

Zheng Zou, Xiaojun Bi, Huan Ma, Ligang Chen, Hai Jin, Shun Gong, Xinning Li, Xiyu Liu

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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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

8 authors.

Zheng Zou *Department of Neurosurgery, General Hospital of Northern Theater Command, Liaoning, 110016, People's Republic of China.
Xiaojun Bi *Department of Urology, General Hospital of Northern Theater Command, Liaoning, 110016, People's Republic of China.
Huan MaThe Fourth Affiliated Hospital, China Medical University, Liaoning, 110031, People's Republic of China.
Ligang ChenDepartment of Neurosurgery, General Hospital of Northern Theater Command, Liaoning, 110016, People's Republic of China.
Hai JinDepartment of Neurosurgery, General Hospital of Northern Theater Command, Liaoning, 110016, People's Republic of China.
Shun GongDepartment of Neurosurgery, General Hospital of Northern Theater Command, Liaoning, 110016, People's Republic of China.
Xinning LiDepartment of Neurosurgery, General Hospital of Northern Theater Command, Liaoning, 110016, People's Republic of China.
Xiyu LiuDepartment of Neurosurgery, General Hospital of Northern Theater Command, Liaoning, 110016, People's Republic of China.ORCID 0009-0002-2778-9665

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atherosclerosis (AS) is a complex, multifactorial cardiovascular disease characterized by lipid accumulation, chronic inflammation, oxidative stress, and endothelial dysfunction. Conventional therapies, including lipid-lowering and anti-inflammatory agents, offer limited efficacy due to inadequate lesion targeting, low bioavailability, and systemic side effects. Nanozymes, which engineered nanomaterials with intrinsic enzyme-mimetic catalytic activities have recently emerged as a transformative therapeutic strategy capable of simultaneously modulating oxidative stress, inflammation, and lipid metabolism. This review comprehensively summarizes recent advances in nanozyme-based interventions for AS, focusing on representative systems such as Prussian blue, cerium oxide, selenium-based, and multifunctional composite nanozymes. We critically discuss their design principles, catalytic mechanisms, lesion-targeting strategies, and therapeutic outcomes in preclinical models. Additionally, we highlight key translational challenges, including biosafety concerns, pharmacokinetic limitations, and manufacturing standardization, which currently impede clinical application. By integrating catalytic activity with targeted delivery and microenvironment-responsive functionalities, nanozymes offer a promising paradigm for precision therapy in AS. Future research should prioritize enhancing biocompatibility, optimizing therapeutic specificity, and establishing scalable, reproducible fabrication methods to facilitate clinical translation. This review aims to provide a systematic framework and insightful guidance for advancing nanozyme-based therapeutics toward clinical application in cardiovascular disease management.

Indexed as

AtherosclerosisNanostructuresAnimalsCatalysisCeriumFerrocyanidesHumansLipid MetabolismOxidative StressSeleniumceric oxideCeriumferric ferrocyanideFerrocyanidesSeleniumatherosclerosisdrug deliverynanomedicinenanozymes

Identifiers

PMID40755466
PMCPMC12317701

What OpenQuestion holds

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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.