Evidence map›Paper›PMID 38090364›Full record

ReviewInternational journal of nanomedicine2023

Biomembrane-Derived Nanoparticles in Alzheimer's Disease Therapy: A Comprehensive Review of Synthetic Lipid Nanoparticles and Natural Cell-Derived Vesicles.

Chao Gao, Yan Liu, Ting-Lin Zhang, Yi Luo, Jie Gao, Jian-Jian Chu, Bao-Feng Gong, Xiao-Han Chen, Tong Yin, Jian Zhang and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of nanomedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 27% of its field
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

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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  8. Nanotherapy of Glioblastoma-Where Hope Grows.International journal of molecular sciences · 2025
    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

11 authors at 4 institutions in 2 countries.

Chao Gao *Department of Neurology, Second Affiliated Hospital (Shanghai Changzheng Hospital) of Naval Medical University, Shanghai, People's Republic of China.
Yan Liu *Department of Clinical Pharmacy, Shanghai Jiao Tong University of Medicine, Shanghai, People's Republic of China.
Ting-Lin Zhang *Changhai Clinical Research Unit, Shanghai Changhai Hospital of Naval Medical University, Shanghai, People's Republic of China.
Yi Luo *Department of Clinical Pharmacy, Shanghai Jiao Tong University of Medicine, Shanghai, People's Republic of China.
Jie Gao *Changhai Clinical Research Unit, Shanghai Changhai Hospital of Naval Medical University, Shanghai, People's Republic of China.
Jian-Jian ChuDepartment of Neurology, Second Affiliated Hospital (Shanghai Changzheng Hospital) of Naval Medical University, Shanghai, People's Republic of China.
Bao-Feng GongDepartment of Neurology, Second Affiliated Hospital (Shanghai Changzheng Hospital) of Naval Medical University, Shanghai, People's Republic of China.
Xiao-Han ChenDepartment of Neurology, Second Affiliated Hospital (Shanghai Changzheng Hospital) of Naval Medical University, Shanghai, People's Republic of China.
Tong YinDepartment of Neurology, Second Affiliated Hospital (Shanghai Changzheng Hospital) of Naval Medical University, Shanghai, People's Republic of China.
Jian ZhangDepartment of Clinical Pharmacy, Shanghai Jiao Tong University of Medicine, Shanghai, People's Republic of China.
You YinDepartment of Neurology, Second Affiliated Hospital (Shanghai Changzheng Hospital) of Naval Medical University, Shanghai, People's Republic of China.
Shanghai Changzheng Hospital · CNShanghai Jiao Tong University · CNChanghai Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current therapies for Alzheimer's disease used in the clinic predominantly focus on reducing symptoms with limited capability to control disease progression; thus, novel drugs are urgently needed. While nanoparticles (liposomes, high-density lipoprotein-based nanoparticles) constructed with synthetic biomembranes have shown great potential in AD therapy due to their excellent biocompatibility, multifunctionality and ability to penetrate the BBB, nanoparticles derived from natural biomembranes (extracellular vesicles, cell membrane-based nanoparticles) display inherent biocompatibility, stability, homing ability and ability to penetrate the BBB, which may present a safer and more effective treatment for AD. In this paper, we reviewed the synthetic and natural biomembrane-derived nanoparticles that are used in AD therapy. The challenges associated with the clinical translation of biomembrane-derived nanoparticles and future perspectives are also discussed.

Indexed as

Alzheimer DiseaseNanoparticlesBlood-Brain BarrierHumansLiposomesLipid NanoparticlesLiposomesAlzheimer’s diseasebionanotechnologyblood‒brain barrierliposomesnanoparticlesneurodegenerative diseases

Identifiers

PMID38090364
PMCPMC10712251
OpenAlexW4389451932

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.