Evidence map›Paper›PMID 37807265›Full record

ArticleACS nano2023

Engineered Selenium/Human Serum Albumin Nanoparticles for Efficient Targeted Treatment of Parkinson's Disease via Oral Gavage.

Kai Xu, Peng Huang, Yixuan Wu, Teng Liu, Ningyi Shao, Lulu Zhao, Xiaoyan Hu, Junlei Chang, Yongbo Peng, Shaogang Qu

Open access · hybridAbstract read
In one paragraph

Article in ACS nano, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
11.0field-weighted citation impact, top 1% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Kai XuDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China.
Peng HuangDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China.
Yixuan WuDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China.
Teng LiuDepartment of Neonatology and Pediatrics, Xiangya Hospital of Central South University, Changsha, Hunan 410008, China.
Ningyi ShaoCancer Centre, Faculty of Health Sciences, University of Macau, Taipa, Macau Special Administrative Region 999078, China.
Lulu ZhaoChongqing Key Laboratory for Pharmaceutical Metabolism Research, The Key Laboratory of Biochemistry and Molecular Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing 400016, China.
Xiaoyan HuShenzhen Key Laboratory of Biomimetic Materials and Cellular Immunomodulation, Institute of Biomedicine and Biotechnology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, Guangdong 518055, China.
Junlei ChangShenzhen Key Laboratory of Biomimetic Materials and Cellular Immunomodulation, Institute of Biomedicine and Biotechnology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, Guangdong 518055, China.
Yongbo PengChongqing Key Laboratory for Pharmaceutical Metabolism Research, The Key Laboratory of Biochemistry and Molecular Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing 400016, China.
Shaogang QuDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China.ORCID 0000-0002-0647-3701
Nanfang Hospital · CNChinese Academy of Sciences · CNChongqing Medical and Pharmaceutical College · CNCentral South University · CNGanzhou People's Hospital · CNUniversity of Macau · MO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a neurodegenerative disorder characterized by the degeneration of dopamine (DA) neurons in the midbrain substantia nigra pars compacta (SNpc). While existing therapeutic strategies can alleviate PD symptoms, they cannot inhibit DA neuron loss. Herein, a tailor-made human serum albumin (HSA)-based selenium nanosystem (HSA/Se nanoparticles, HSA/Se NPs) to treat PD that can overcome the intestinal epithelial barrier (IEB) and blood-brain barrier (BBB) is described. HSA, a transporter for drug delivery, has superior biological characteristics that make it an ideal potential drug delivery substance. Findings reveal that HSA/Se NPs have lower toxicity and higher efficacy than other selenium species and the ability to overcome the IEB and BBB to enrich DA neurons, which then protect MN9D cells from MPP

Indexed as

NanoparticlesParkinson DiseaseSeleniumAnimalsDisease Models, AnimalDopaminergic NeuronsHumansMiceMice, Inbred C57BLSeleniumhuman serum albuminnanosystemParkinson’s diseaseseleniumtreatment

Identifiers

PMID37807265
PMCPMC10604087
OpenAlexW4387439452

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.