Evidence map›Paper›PMID 39427214›Full record

ArticleJournal of nanobiotechnology2024

Single-atom nanozyme liposome-integrated microneedles for in situ drug delivery and anti-inflammatory therapy in Parkinson's disease.

Ying Liu, Ye Liu, Peimiao Shi, Xiaopeng Hu, Xiaowan Fan, Yalong Wu, Jiangpeng Pan, Qian Bai, Qing Li

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

9 authors.

Ying Liu *Medical Research Center, The Second Affiliated Hospital of Zhengzhou University, Henan, 450000, China.
Ye Liu *Department of Anaesthesiology, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, 100026, China.
Peimiao ShiThe Affiliated Tengzhou Central People's Hospital of Xuzhou Medical University, Shandong, 277500, China.
Xiaopeng HuMedical Research Center, The Second Affiliated Hospital of Zhengzhou University, Henan, 450000, China.
Xiaowan FanMedical Research Center, The Second Affiliated Hospital of Zhengzhou University, Henan, 450000, China.
Yalong WuHenan Key Laboratory of Chronic Disease Management, Henan Provincial People's Hospital, Central China Fuwai Hospital of Zhengzhou University, Henan, 450000, China.
Jiangpeng PanHenan Key Laboratory of Chronic Disease Management, Henan Provincial People's Hospital, Central China Fuwai Hospital of Zhengzhou University, Henan, 450000, China.
Qian BaiMedical Research Center, The Second Affiliated Hospital of Zhengzhou University, Henan, 450000, China.
Qing LiMedical Research Center, The Second Affiliated Hospital of Zhengzhou University, Henan, 450000, China. lq1515012032@163.com.

Funding

Joint Project of Medical Science and Technology of Henan Province LHGJ20220498Young and Middle-Aged Academic Leaders of Health in Henan Province HNSWJW-2021001Youth Science Foundation Project of Henan Province 232300421285
6 · The paper itself

Abstract

Treatment for Parkinson's disease (PD) has been impeded by inefficient treatment results and multiple membrane barriers during drug delivery. This study reports the design, synthesis, and application of microneedles (MNs) loaded with mitochondrion-targeted liposome encapsulated iron (Fe)-isolated single-atom nanozymes (Mito@Fe-ISAzyme, MFeI), called MFeI MNs, for in situ drug delivery into the brain parenchyma and efficient enrichment of drugs in lesion sites. In in vitro experiments, MFeI can scavenge reactive oxygen species (ROS) and protect the neurons via mitochondrial targeting, guaranteeing the subsequent treatment of PD. Using PD mouse models, we compared the intravenous injection of MFeI with the brain in situ administration of MFeI MNs (in situ MFeI MNs). Results showed that in situ MFeI MNs significantly improved the deep penetration of the drug into brain parenchyma, especially in the vital pathological sites such as the substantia nigra pars compacta and striatum. Importantly, ROS elimination and neuroinflammatory remission in the lesion site were observed, thereby efficiently alleviating the behavioral disorders and pathological symptoms of PD mice. Therefore, the MNs system for in situ single-atom nanozyme liposome delivery exhibits great potential in PD treatment.

Indexed as

Anti-Inflammatory AgentsDrug Delivery SystemsLiposomesParkinson DiseaseReactive Oxygen SpeciesAnimalsBrainDisease Models, AnimalIronMaleMiceMice, Inbred C57BLMitochondriaNeedlesAnti-Inflammatory AgentsIronLiposomesReactive Oxygen SpeciesIn situ deliveryMicroneedlesNeuroinflammatory remissionParkinson’s diseaseSingle-atom nanozyme

Identifiers

PMID39427214
PMCPMC11490154

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.