Evidence map›Paper›PMID 32005196›Full record

ArticleJournal of nanobiotechnology2020

Oleic acid-based nanosystems for mitigating acute respiratory distress syndrome in mice through neutrophil suppression: how the particulate size affects therapeutic efficiency.

Huang-Ping Yu, Fu-Chao Liu, Ani Umoro, Zih-Chan Lin, Ahmed O Elzoghby, Tsong-Long Hwang, Jia-You Fang

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
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  3. Low-inflammatory lipid nanoparticles facilitate safe mRNA vaccination against influenza virus infection.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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  8. Scd-1 deficiency promotes the differentiation of CD8Frontiers in cellular and infection microbiology · 2024
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  11. Can natural products modulate cytokine storm in SARS-CoV2 patients?Biotechnology reports (Amsterdam, Netherlands) · 2022
    Review
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  13. Omega-9 fatty acids: potential roles in inflammation and cancer management.Journal, genetic engineering & biotechnology · 2022
    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

7 authors at 4 institutions in 3 countries.

Huang-Ping YuDepartment of Anesthesiology, Chang Gung Memorial Hospital, Kweishan, Taoyuan, Taiwan.
Fu-Chao LiuDepartment of Anesthesiology, Chang Gung Memorial Hospital, Kweishan, Taoyuan, Taiwan.
Ani UmoroGraduate Institute of Natural Products, Chang Gung University, 259 Wen-Hwa 1st Road, Kweishan, 333, Taoyuan, Taiwan.
Zih-Chan LinGraduate Institute of Biomedical Sciences, Chang Gung University, Kweishan, Taoyuan, Taiwan.
Ahmed O ElzoghbyDivision of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Tsong-Long HwangDepartment of Anesthesiology, Chang Gung Memorial Hospital, Kweishan, Taoyuan, Taiwan. htl@mail.cgu.edu.tw.
Jia-You FangDepartment of Anesthesiology, Chang Gung Memorial Hospital, Kweishan, Taoyuan, Taiwan. fajy@mail.cgu.edu.tw.ORCID http://orcid.org/0000-0003-2114-7709
Chang Gung University · TWBrigham and Women's Hospital · USChang Gung University of Science and Technology · TWMing Chi University of Technology · TW

Funding

Chang Gung Memorial Hospital CMRPG3G1601-2Chang Gung Memorial Hospital CMRPG3H0811-3Ministry of Science and Technology, Taiwan MOST-108-2314-B-182A-058-MY2Ministry of Science and Technology, Taiwan (TW) MOST-108-2314-B-182A-059-MY2
6 · The paper itself

Abstract

backgroundOleic acid (OA) is reported to show anti-inflammatory activity toward activated neutrophils. It is also an important material in nanoparticles for increased stability and cellular internalization. We aimed to evaluate the anti-inflammatory activity of injectable OA-based nanoparticles for treating lung injury. Different sizes of nanocarriers were prepared to explore the effect of nanoparticulate size on inflammation inhibition.

resultsThe nanoparticles were fabricated with the mean diameters of 105, 153, and 225 nm. The nanocarriers were ingested by isolated human neutrophils during a 5-min period, with the smaller sizes exhibiting greater uptake. The size reduction led to the decrease of cell viability and the intracellular calcium level. The OA-loaded nanosystems dose-dependently suppressed the superoxide anion and elastase produced by the stimulated neutrophils. The inhibition level was comparable for the nanoparticles of different sizes. In the ex vivo biodistribution study, the pulmonary accumulation of nanoparticles increased following the increase of particle size. The nanocarriers were mainly excreted by the liver and bile clearance. Mice were exposed to intratracheal lipopolysaccharide (LPS) to induce acute respiratory distress syndrome (ARDS), like lung damage. The lipid-based nanocarriers mitigated myeloperoxidase (MPO) and cytokines more effectively as compared to OA solution. The larger nanoparticles displayed greater reduction on MPO, TNF-α, and IL-6 than the smaller ones. The histology confirmed the decreased pulmonary neutrophil recruitment and lung-architecture damage after intravenous administration of larger nanoparticles.

conclusionsNanoparticulate size, an essential property governing the anti-inflammatory effect and lung-injury therapy, had different effects on activated neutrophil inhibition and in vivo therapeutic efficacy.

Indexed as

AnimalsAnti-Inflammatory AgentsCytokinesDisease Models, AnimalDrug LiberationHumansLipidsLipopolysaccharidesLungMiceMice, Inbred C57BLNanocapsulesNeutrophil ActivationNeutrophilsOleic AcidPancreatic ElastaseAnti-Inflammatory AgentsCytokinesLipidsLipopolysaccharidesNanocapsulesOleic AcidPancreatic ElastasePeroxidaseSuperoxidesAcute respiratory distress syndromeAnti-inflammationLipid-based nanoparticlesNeutrophilOleic acidSize

Identifiers

PMID32005196
PMCPMC6995149
OpenAlexW3010442855

What OpenQuestion holds

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LicenceCC BY
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.