Evidence map›Paper›PMID 40717066›Full record

ReviewJournal of nanobiotechnology2025

Nanomedicine in cardiovascular and cerebrovascular diseases: targeted nanozyme therapies and their clinical potential and current challenges.

Yanhua Jiang, Yongjian Zhou, Zhe Li, Liang Guo

Abstract readReview
In one paragraph

Review in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Immunomodulatory Nanozymes as Programmable Redox-Immune Set-Point Regulators.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Review
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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

4 authors.

Yanhua Jiang *Department of Anesthesiology, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China, Shenyang, China.
Yongjian Zhou *Department of Anesthesiology, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China, Shenyang, China.
Zhe LiDepartment of Anesthesiology, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China, Shenyang, China. jllizhe@126.com.
Liang GuoDepartment of Cardiology, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China, Shenyang, China. lguo@cmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular and cerebrovascular diseases continue to be significant public health problems, with high mortality and morbidity rates worldwide. Inflammation and ROS are believed to be the hallmarks of these diseases, but conventional therapies targeting inflammation and ROS have had limited success due to their limited pharmacokinetics, low bioavailability, shorter half-life, and notable side effects. Over the last decade, nanomedicine has rapidly evolved with diverse applications in diagnostics, drug delivery, and treatment of various diseases, including cardiovascular and cerebrovascular diseases. Nanomaterials such as nanozymes have gained success with remarkable therapeutic efficacy due to their stability, formulations, enzyme-mimetic activities, and ability to deliver more than one drug. Moreover, nanozymes can uphold a constant rate of drug release, maintaining a low frequency of dosing to reduce the side effects of drugs. Due to their multifunctional nature, they can be used as targeted delivery vehicles to the damaged brain, arterial, and other tissues to mitigate inflammation and ROS while promoting blood-brain barrier protection, ischemic stroke neurovascular recovery, and neuronal cell survival. In this review article, we have explored the mechanisms and different types of nanozyme-based targeted therapies for several cardiovascular and cerebrovascular diseases, including myocardial infarction, atherosclerosis, and ischemic stroke. We have discussed their enzyme-mimetic catalytic activities, immune-modulatory effects, ROS scavenging abilities, and anti-inflammatory properties. We have also discussed the challenges that slow down the clinical and translational success of these nanozyme-based therapies. Continuing work with integrated and multidisciplinary approaches, these nanozymes may offer potential solutions for cardiovascular and cerebrovascular diseases.

Indexed as

Cardiovascular DiseasesCerebrovascular DisordersNanomedicineNanostructuresAnimalsAnti-Inflammatory AgentsBlood-Brain BarrierDrug Delivery SystemsHumansReactive Oxygen SpeciesAnti-Inflammatory AgentsReactive Oxygen SpeciesAnti-inflammationCardiovascular diseasesCerebrovascular diseasesNanozymesROS

Identifiers

PMID40717066
PMCPMC12302787

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.