Evidence map›Paper›PMID 40470331›Full record

ArticleInnovation (Cambridge (Mass.))2025

A polymerized probucol nanoformulation with neutrophil extracellular vesicle camouflage for cerebral ischemia-reperfusion injury therapy.

Mengjie Jia, Wenjun Miao, Yiliang Li, Yajie Guo, Jieying Zeng, Yan Gao, Xinting Li, Yufan Wang, Zhenghuan Zhao, Zichen Xu and 5 more

Abstract read
In one paragraph

Article in Innovation (Cambridge (Mass.)), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. 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

15 authors.

Mengjie JiaSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Wenjun MiaoSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Yiliang LiThe Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, China.
Yajie GuoSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Jieying ZengSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Yan GaoSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Xinting LiSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Yufan WangSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Zhenghuan ZhaoSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Zichen XuJinfeng Laboratory, Chongqing 401329, China.
Nancy WangSchool of Clinical Medicine, The University of Cambridge, CB2 0SP Cambridge, UK.
Fang YangJiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210009, China.
Jing ZhaoSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Yi WangSchool of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
Guixue WangJinfeng Laboratory, Chongqing 401329, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study leverages the unique advantages of polyprodrug systems and biomimetic technology to develop a novel biomimetic nanoformulation, in which neutrophil extracellular vesicles (NEVs) are coated onto reactive oxygen species (ROS)-sensitive probucol-based polyprodrug nanoparticles (NPPBNPs). This NEV-camouflaged biomimetic nanoformulation holds significant potential for the effective treatment of cerebral ischemia-reperfusion injury (CIRI), offering multifaceted therapeutic effects, such as ROS elimination, inhibition of oxidative stress-induced neuronal apoptosis, attenuation of glial hyperactivation, and suppression of pro-inflammatory mediator secretion. In a murine CIRI model, NPPBNPs markedly enhanced neuronal viability, ameliorated the ischemic penumbra, restored behavioral functions, and exhibited an acceptable safety profile. The therapeutic mechanism of NPPBNPs involves NEV-mediated camouflage, which enables selective targeting of the pathological endothelium, thereby reducing peripheral neutrophil recruitment and facilitating blood-brain barrier (BBB) transport. Upon internalization by neurons, astrocytes, and microglia within ischemic regions, NPPBNPs respond to elevated intracellular ROS levels by releasing probucol in a controlled manner, which synergistically mitigates oxidative stress and inflammatory responses in CIRI-affected areas. Collectively, this multifunctional biomimetic nanoformulation represents a promising and practical strategy for the safe and effective treatment of CIRI.

Identifiers

PMID40470331
PMCPMC12131010

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Registered trials

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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.