Cited by 205Extracellular vesicles in diseaseNanoparticle-Based Drug DeliveryAdvanced Drug Delivery Systems

Intranasal Administration of Self-Oriented Nanocarriers Based on Therapeutic Exosomes for Synergistic Treatment of Parkinson’s Disease

Peng, Huan, Li, Yan, Ji, Weihong, Zhao, Ruichen, Lu, Zhiguo, Shen, Jie, Wu, Yanyue, Wang, Jianze +5 more·2022·ACS Nano

Abstract

The treatment of Parkinson's disease (PD) has been hindered by the complex pathologies and multiple membrane barriers during drug delivery. Although exosomes derived from mesenchymal stem cells (MSCs) have great potential for PD, MSC-derived exosomes alone could not fully meet the therapeutic requirements due to their limitation in therapy and delivery. Here, we develop a self-oriented nanocarrier called PR-EXO/PP@Cur that combines therapeutic MSC-derived exosomes with curcumin. PR-EXO/PP@Cur can be self-oriented across the multiple membrane barriers and directly release drugs into the cytoplasm of target cells after intranasal administration. With enhanced accumulation of drugs in the action site, PR-EXO/PP@Cur achieves three-pronged synergistic treatment to deal with the complex pathologies of PD by reducing α-synuclein aggregates, promoting neuron function recovery, and alleviating the neuroinflammation. After treatment with PR-EXO/PP@Cur, the movement and coordination ability of PD model mice are significantly improved. These results show that PR-EXO/PP@Cur has great prospects in treatment of PD or other neurodegenerative diseases.

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Registry

Crossref · 10.1021/acsnano.1c08473

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1 of 1 references verified0 citation errors · 0 not checkable

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  • In a PD mouse model, PR-EXO/PP@Cur decreased the concentration of α-syn aggregates, increased the amount of dopaminergic neurons in the substantia nigra, and improved motor function.

    “In a PD mouse model, the PR-EXO/PP@Cur decreased the concentration of α-syn aggregates and increased the amount of dopaminergic neurons in the substantia nigra, and improved the motor function of the PD mice [262].”

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Authors
Peng, H., Li, Y., Ji, W., Zhao, R., Lu, Z., Shen, J., Wu, Y., Wang, J., Hao, Q., Wang, J., Wang, W., Yang, J., & Zhang, X.
Affiliations
  • Chinese Academy of Sciences (CN)
  • University of Science and Technology Beijing (CN)
  • State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, PR China
Corresponding author
Zhang, Xin
Venue
ACS Nano
Published
2022-01-05
Volume
16
Issue
1
Pages
869-884
ISSN
  • 1936-0851 (ISSN-L)
  • 1936-086X
OpenAlex
W4206764354
Cited by
205
References
1
Citations by year
2026: 30 · 2025: 59 · 2024: 58 · 2023: 45 · 2022: 13
FWCI
14.29
Type
journal article
Language
en
Open access
closed
Locations
  • ACS Nano (publishedVersion)
  • PubMed (publishedVersion)
  • Institute of Process Engineering, CAS Institutional Repository (submittedVersion)
Funders
  • Natural Science Foundation of Beijing Municipality (2192057)
  • National Natural Science Foundation of China (21875254, 21905283, 22075289, 31771095, 32071391, 52073287)
  • Beijing Nova Program (Z201100006820140)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
Keywords
Parkinson's disease, mesenchymal stem cell-derived exosomes, intranasal drug delivery, curcumin, alpha-synuclein aggregation, neuroinflammation, neuroprotection, synergistic therapy, neurodegenerative diseases
MeSH terms
Administration, Intranasal, Animals, Curcumin, Parkinson Disease, Mice, Exosomes, Mesenchymal Stem Cells

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