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Nanoparticles in Vascular Dementia: Advantages and Challenges.

Nanoparticles in Vascular Dementia: Advantages and Challenges.

期刊: CNS neuroscience & therapeutics 日期: 2026-06-01 PMID: 42237946 DOI: 10.1002/cns.70966 浏览: 31
作者: Liu X, Hu J, Qiu Y, Wang H, Shen C, Liu Z, He Y, Du X, Zhang X
X, L., J, H., Y, Q., H, W., C, S., Z, L., Y, H., X, D., & X, Z. (2026). Nanoparticles in Vascular Dementia: Advantages and Challenges.. CNS neuroscience & therapeutics. https://doi.org/10.1002/cns.70966
X L, J H, Y Q, H W, C S, Z L, et al. Nanoparticles in Vascular Dementia: Advantages and Challenges.. CNS neuroscience & therapeutics. 2026; doi: 10.1002/cns.70966
X L, J H, Y Q, et al. Nanoparticles in Vascular Dementia: Advantages and Challenges.[J]. CNS neuroscience & therapeutics. 2026. DOI: 10.1002/cns.70966.
@article{x2026,
  author = {Liu X and Hu J and Qiu Y and Wang H and Shen C and Liu Z and He Y and Du X and Zhang X},
  title = {Nanoparticles in Vascular Dementia: Advantages and Challenges.},
  journal = {CNS neuroscience & therapeutics},
  year = {2026},
  doi = {10.1002/cns.70966},
  note = {PMID: 42237946},
}
TY  - JOUR
AU  - Liu X
AU  - Hu J
AU  - Qiu Y
AU  - Wang H
AU  - Shen C
AU  - Liu Z
AU  - He Y
AU  - Du X
AU  - Zhang X
TI  - Nanoparticles in Vascular Dementia: Advantages and Challenges.
T2  - CNS neuroscience & therapeutics
PY  - 2026
DO  - 10.1002/cns.70966
AN  - PMID:42237946
ER  - 

摘要

BACKGROUND: Vascular dementia (VaD) is the second most prevalent form of dementia, accounting for 15%-20% of dementia cases and is primarily caused by cerebrovascular disorders. Current treatments predominantly focus on risk factor management and symptom alleviation, lacking the ability to cure the disease or reverse cognitive decline, which underscores the urgent need for novel therapeutic approaches like nanotechnology. METHODS: This paper provides a comprehensive review integrating materials science, clinical medicine, and bioinformatics to evaluate the current status of nanomaterial research in VaD. It focuses on the molecular mechanisms of action of various nanomaterials and provides an analysis of their therapeutic potential and future development challenges. RESULTS: In diagnostic applications, nanomaterials (e.g., SPIONs and fluorescent nanoparticles) enable high-contrast imaging of early-stage vascular inflammation, blood-brain barrier (BBB) leakage, and amyloid β (Aβ) deposits. In therapeutic applications, engineered nanocarriers (including liposomes, polymeric nanoparticles, and gold nanoparticles) exhibit specific targeting, controlled release, and BBB penetration capabilities. They mitigate VaD pathology by promoting angiogenesis, scavenging reactive oxygen species (ROS) to reduce oxidative stress, inhibiting neuroinflammation, protecting the neurovascular unit (NVU), and facilitating white matter repair. CONCLUSION: Nanotechnology provides an innovative framework for the diagnosis and treatment of VaD through intelligent, targeted drug delivery systems. Future advancements require establishing systematic biocompatibility evaluation frameworks, addressing long-term toxicity concerns, and expanding multicenter clinical trials to validate safety and efficacy for clinical translation.

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