Evidence map›Paper›PMID 28740387›Full record

ArticleInternational journal of nanomedicine2017

Apatinib-loaded nanoparticles suppress vascular endothelial growth factor-induced angiogenesis and experimental corneal neovascularization.

Jung Eun Lee, Koung Li Kim, Danbi Kim, Yeongju Yeo, Hyounkoo Han, Myung Goo Kim, Sun Hwa Kim, Hyuncheol Kim, Ji Hoon Jeong, Wonhee Suh

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  3. Albumin Nanoparticle-Based Drug Delivery Systems.International journal of nanomedicine · 2024
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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

10 authors at 4 institutions in 1 country.

Jung Eun LeeSchool of Pharmacy, Sungkyunkwan University, Suwon.
Koung Li KimCollege of Pharmacy, Chung-Ang University, Seoul.
Danbi KimCollege of Pharmacy, Chung-Ang University, Seoul.
Yeongju YeoCollege of Pharmacy, Chung-Ang University, Seoul.
Hyounkoo HanDepartment of Chemical and Biomolecular Engineering, Sogang University.
Myung Goo KimSchool of Pharmacy, Sungkyunkwan University, Suwon.
Sun Hwa KimCenter for Theragnosis Biomedical Research Institute, Korea Institute of Science and Technology (KIST).
Hyuncheol KimDepartment of Chemical and Biomolecular Engineering, Sogang University.
Ji Hoon JeongSchool of Pharmacy, Sungkyunkwan University, Suwon.
Wonhee SuhCollege of Pharmacy, Chung-Ang University, Seoul.
Chung-Ang University · KRSogang University · KRKorea Institute of Science and Technology · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathological angiogenesis is one of the major symptoms of severe ocular diseases, including corneal neovascularization. The blockade of vascular endothelial growth factor (VEGF) action has been recognized as an efficient strategy for treating corneal neovascularization. In this study, we aimed to investigate whether nanoparticle-based delivery of apatinib, a novel and selective inhibitor of VEGF receptor 2, inhibits VEGF-mediated angiogenesis and suppresses experimental corneal neovascularization. Water-insoluble apatinib was encapsulated in nanoparticles composed of human serum albumin (HSA)-conjugated polyethylene glycol (PEG). In vitro angiogenesis assays showed that apatinib-loaded HSA-PEG (Apa-HSA-PEG) nanoparticles potently inhibited VEGF-induced tube formation, scratch wounding migration, and proliferation of human endothelial cells. In a rat model of alkali burn injury-induced corneal neovascularization, a subconjunctival injection of Apa-HSA-PEG nanoparticles induced a significant decrease in neovascularization compared to that observed with an injection of free apatinib solution or phosphate-buffered saline. An in vivo distribution study using HSA-PEG nanoparticles loaded with fluorescent hydrophobic model drugs revealed the presence of a substantial number of nanoparticles in the corneal stroma within 24 h after injection. These in vitro and in vivo results demonstrate that apatinib-loaded nanoparticles may be promising for the prevention and treatment of corneal neovascularization-related ocular disorders.

Indexed as

Angiogenesis Inducing AgentsAnimalsCorneal NeovascularizationDisease Models, AnimalEndothelial CellsHumansHuman Umbilical Vein Endothelial CellsNanoparticlesNeovascularization, PathologicPolyethylene GlycolsPyridinesRats, Sprague-DawleySerum AlbuminVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2Angiogenesis Inducing AgentsapatinibPolyethylene GlycolsPyridinesSerum AlbuminVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2apatinibcorneal neovascularizationnanoparticlevascular endothelial growth factor

Identifiers

PMID28740387
PMCPMC5503670
OpenAlexW2727700849

What OpenQuestion holds

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LicenceCC BY-NC
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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.