Evidence map›Paper›PMID 23849876›Full record

ArticleBiomaterials2013

Long-term suppression of ocular neovascularization by intraocular injection of biodegradable polymeric particles containing a serpin-derived peptide.

Ron B Shmueli, Masayuki Ohnaka, Akiko Miki, Niranjan B Pandey, Raquel Lima e Silva, Jacob E Koskimaki, Jayoung Kim, Aleksander S Popel, Peter A Campochiaro, Jordan J Green

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
7.4field-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.

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

24 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Experimental and mathematical approaches for drug delivery for the treatment of wet age-related macular degeneration.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Gene delivery nanoparticles to modulate angiogenesis.Advanced drug delivery reviews · 2017
    Review
  15. Article
  16. A Critical Analysis of the AvailableJournal of ophthalmology · 2017
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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 2 institutions in 1 country.

Ron B ShmueliDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Masayuki Ohnaka
Akiko Miki
Niranjan B Pandey
Raquel Lima e Silva
Jacob E Koskimaki
Jayoung Kim
Aleksander S Popel
Peter A Campochiaro
Jordan J Green
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

Targeting survival factors for ocular neovascularizationR01EY012609 · NEI · JOHNS HOPKINS UNIVERSITY · PI CAMPOCHIARO, PETER A · 1999 to 2015
$5.3M
Biodegradable serpin-peptide-carrying nano- and microparticles for wet AMDR21EY022986 · NEI · JOHNS HOPKINS UNIVERSITY · PI GREEN, JORDAN · 2013 to 2014
$441k
NEI NIH HHS 1R21EY022986-01NEI NIH HHS R01 EY012609NEI NIH HHS R01EY012609NEI NIH HHS R21 EY022986
6 · The paper itself

Abstract

Aberrant angiogenesis can cause or contribute to a number of diseases such as neovascular age-related macular degeneration (NVAMD). While current NVAMD treatments target angiogenesis, these treatments are not effective for all patients and also require frequent intravitreal injections. New agents and delivery systems to treat NVAMD could be beneficial to many patients. We have recently developed a serpin-derived peptide as an anti-angiogenic agent. Here, this peptide is investigated for activity in human retinal endothelial cells in vitro and for reducing angiogenesis in a laser-induced choroidal neovascularization mouse model of NVAMD in vivo. While frequent intravitreal injections can be tolerated clinically, reducing the number of injections can improve patient compliance, safety, and outcomes. To achieve this goal, and to maximize the in vivo activity of injected peptide, we have developed biodegradable polymers and controlled release particle formulations to extend anti-angiogenic therapy. To create these devices, the anionic peptides are first self-assembled into nanoparticles using a biodegradable cationic polymer and then as a second step, these nanoparticles are encapsulated into biodegradable poly(lactic-co-glycolic acid) (PLGA) microparticles. In situ, these particles show approximately zero-order, linear release of the anionic peptide over 200 days. These particles are made of safe, hydrolytically degradable polymers and have low endotoxin. Long-term in vivo experiments in the laser-induced neovascularization model for NVAMD show that these peptide-releasing particles decrease angiogenesis for at least fourteen weeks in vivo following a single particle dose and therefore are a promising treatment strategy for NVAMD.

Indexed as

AnimalsBiocompatible MaterialsBiodegradation, EnvironmentalChoroidal NeovascularizationEndothelial CellsFemaleHumansIntravitreal InjectionsLactic AcidMiceMice, Inbred C57BLNanoparticlesPeptidesPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersBiocompatible MaterialsLactic AcidPeptidespoly(beta-amino ester)Polyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersSerpinsAngiogenesisControlled drug releaseDrug deliveryMicrosphereOphthalmologyPeptide

Identifiers

PMID23849876
PMCPMC3838902
OpenAlexW2158455128

What OpenQuestion holds

Textmetadata
LicenceTDM
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.