Evidence map›Paper›PMID 39425199›Full record

ArticleJournal of nanobiotechnology2024

A novel biomimetic nanovesicle containing caffeic acid-coupled carbon quantum dots for the the treatment of Alzheimer's disease via nasal administration.

Yu Hu, Jingwen Cui, Junpeng Sun, Xiaobang Liu, Shuang Gao, Xifan Mei, Chao Wu, He Tian

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Nanoparticles as an Encouraging Therapeutic Approach to Alzheimer's Disease.International journal of molecular sciences · 2025
    Review
  10. Review
  11. Review
  12. Carbon dots derived fromFrontiers in molecular biosciences · 2025
    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

8 authors.

Yu Hu *School of Basic Medicine, Jinzhou Medical University, Jinzhou, Liaoning, 121001, China.
Jingwen CuiThe First Affiliated Hospital of Jinzhou Medical University, Jinzhou, Liaoning, 121001, China.
Junpeng SunPharmacy School, Jinzhou Medical University, Jinzhou, Liaoning, 121001, China.
Xiaobang LiuPharmacy School, Jinzhou Medical University, Jinzhou, Liaoning, 121001, China.
Shuang GaoSchool of Basic Medicine, Jinzhou Medical University, Jinzhou, Liaoning, 121001, China.
Xifan Mei *Liaoning Vocational College of Medicine, Shenyang, Liaoning, 110101, China. meixifan@jzmu.edu.cn.
Chao Wu *Liaoning Provincial Collaborative Innovation Center for Medical Testing and Drug Research, Jinzhou Medical University, Jinzhou, Liaoning, 121001, China. wuchao@jzmu.edu.cn.
He Tian *School of Basic Medicine, Jinzhou Medical University, Jinzhou, Liaoning, 121001, China. tianhe@jzmu.edu.cn.

Funding

Basic Research Projects of Higher Education Institutions by Liaoning Provincial Department of Education NO. jytms20231734
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a common neurodegenerative disease characterized by progressive cognitive and physical impairment. Neuroinflammation is related to AD, and the misfolding and aggregation of amyloid protein in the brain creates an inflammatory microenvironment. Microglia are the predominant contributors to neuroinflammation, and abnormal activation of microglia induces the release of a large amount of inflammatory factors, promotes neuronal apoptosis, and leads to cognitive impairment. In this study, we used microglial membranes containing caffeic acid-coupled carbon quantum dots to prepare a novel biomimetic nanocapsule (CDs-CA-MGs) for the treatment of AD. The application of CDs-CA-MGs via nasal administration can bypass the blood‒brain barrier (BBB) and directly target the site of inflammation. After treatment with CDs-CA-MGs, AD mice showed reduced inflammation in the brain, decreased neuronal apoptosis, and significantly improved learning and memory abilities. In addition, CDs-CA-MGs affect inflammation-related JAK-STAT and Toll-like receptor signaling pathways in AD mice. CDs-CA-MGs significantly downregulated interleukins (IL-1β and IL-6) and tumor necrosis factor (TNF-α). This finding suggested that CDs-CA-MGs may improve cognitive impairment by modulating inflammatory responses. In conclusion, the use of CDs-CA-MGs provides a possible therapeutic strategy for the treatment of AD.

Indexed as

Administration, IntranasalAlzheimer DiseaseCaffeic AcidsCarbonQuantum DotsAnimalsApoptosisBiomimetic MaterialsBiomimeticsBrainDisease Models, AnimalMaleMiceMicrogliacaffeic acidCaffeic AcidsCarbonAlzheimer’s diseaseCaffeic acidCarbon quantum dotsMicrogliaNeuroinflammation

Identifiers

PMID39425199
PMCPMC11490022

What OpenQuestion 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 OpenQuestion graph.