Evidence map›Paper›PMID 19194480›Full record

ArticleGene therapy2009

Intravenous transferrin, RGD peptide and dual-targeted nanoparticles enhance anti-VEGF intraceptor gene delivery to laser-induced CNV.

S R Singh, H E Grossniklaus, S J Kang, H F Edelhauser, B K Ambati, U B Kompella

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Gene therapy, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02042027 (Subconjunctival IVIg), which is not on this map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
5.8field-weighted citation impact, top 3% 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.

NCT02042027 phase1withdrawnnot on this mapstarted 2014, after this paper: background citation

Subconjunctival IVIg (Gamunex-C) Injection for Corneal Neovascularization and Inflammatory Conditions

TypeinterventionalSponsorUniversity of UtahRan2014 to 2016Enrolled0ConditionsCorneal Neovascularization, Corneal Graft Failure, Anterior Segment InflammationArmsGamunex-C
3 · Its place in the literature

Who cites it

76 citing papers in PubMed, 201 citations in OpenAlex.

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  20. Biomedical nanoparticle design: What we can learn from viruses.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Review

16 more citing papers are in PubMed but not listed here.

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

6 authors at 5 institutions in 1 country.

S R SinghDepartment of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, NE, USA.
H E Grossniklaus
S J Kang
H F Edelhauser
B K Ambati
U B Kompella
Emory Eye Center · USEmory University · USEye Institute of Utah · USUniversity of Colorado Denver · USUniversity of Nebraska Medical Center · US

Funding

P30-Core Grant for Vision Research Core CP30EY006360 · NEI · EMORY UNIVERSITY · PI BOATRIGHT, JEFFREY H · 1986 to 2025
$15.3M
Transscleral Drug Delivery for Retinal DisordersR24EY017045 · NEI · EMORY UNIVERSITY · PI EDELHAUSER, HENRY FRANCIS · 2006 to 2010
$6.9M
Intraceptor Interference of VEGF PathwaysR01EY017182 · NEI · UNIVERSITY OF UTAH · PI AMBATI, BALAMURALI K · 2007 to 2017
$3.6M
Delivery of LEDGF for retinal degenerative disordersR21EY017360 · NEI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI KOMPELLA, UDAY B · 2007 to 2008
$395k
NEI NIH HHS 5R01EY017182NEI NIH HHS P30 EY006360NEI NIH HHS R01 EY017182NEI NIH HHS R21 EY017360NEI NIH HHS R24 EY017045
6 · The paper itself

Abstract

Choroidal neovascularization (CNV) leads to loss of vision in age-related macular degeneration (AMD), the leading cause of blindness in adult population over 50 years old. In this study, we developed intravenously administered, nanoparticulate, targeted nonviral retinal gene delivery systems for the management of CNV. CNV was induced in Brown Norway rats using a 532 nm laser. We engineered transferrin, arginine-glycine-aspartic acid (RGD) peptide or dual-functionalized poly-(lactide-co-glycolide) nanoparticles to target delivery of anti-vascular endothelial growth factor (VEGF) intraceptor plasmid to CNV lesions. Anti-VEGF intraceptor is the only intracellularly acting VEGF inhibitory modality. The results of the study show that nanoparticles allow targeted delivery to the neovascular eye but not the control eye on intravenous administration. Functionalizing the nanoparticle surface with transferrin, a linear RGD peptide or both increased the retinal delivery of nanoparticles and subsequently the intraceptor gene expression in retinal vascular endothelial cells, photoreceptor outer segments and retinal pigment epithelial cells when compared to nonfunctionalized nanoparticles. Most significantly, the CNV areas were significantly smaller in rats treated with functionalized nanoparticles as compared to the ones treated with vehicle or nonfunctionalized nanoparticles. Thus, surface-functionalized nanoparticles allow targeted gene delivery to the neovascular eye on intravenous administration and inhibit the progression of laser-induced CNV in a rodent model.

Indexed as

Gene Transfer TechniquesAnimalsChemistry, PhysicalChoroidal NeovascularizationDisease Models, AnimalGenetic TherapyInjections, IntravenousLasersMaleMicroscopy, ConfocalNanoparticlesOligopeptidesRatsRats, Inbred BNReceptors, Vascular Endothelial Growth FactorRetinaarginyl-glycyl-aspartic acidOligopeptidesReceptors, Vascular Endothelial Growth FactorTransferrinVascular Endothelial Growth Factor A

Identifiers

PMID19194480
PMCPMC2993697
OpenAlexW2065691617

What OpenQuestion holds

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Registered trials

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.