Evidence map›Paper›PMID 17923842›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2008

Cell-penetrating peptide for enhanced delivery of nucleic acids and drugs to ocular tissues including retina and cornea.

Leslie N Johnson, Siobhan M Cashman, Rajendra Kumar-Singh

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

62 citing papers in PubMed, 161 citations in OpenAlex.

  1. Mathematical Models of Topically and Intravitreally Applied Ranibizumab.Investigative ophthalmology & visual science · 2025
    Article
  2. Retinal Penetrating Adeno-Associated Virus.Investigative ophthalmology & visual science · 2024
    Article
  3. Article
  4. Long-Acting Ocular Injectables: Are We Looking In The Right Direction?Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  5. Review
  6. Engineered peptide-drug conjugate provides sustained protection of retinal ganglion cells with topical administration in rats.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Peptide cargo administration: current state and applications.Applied microbiology and biotechnology · 2023
    Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review

2 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

3 authors at 1 institution in 1 country.

Leslie N JohnsonDepartment of Ophthalmology, Tufts University School of Medicine, Boston, Massachusetts, USA.
Siobhan M Cashman
Rajendra Kumar-Singh
Tufts University · US

Funding

Gene Therapy for Retinitis PigmentosaR01EY013837 · NEI · UNIVERSITY OF UTAH · PI KUMAR-SINGH, RAJENDRA · 2003 to 2012
$2.7M
Non-Viral Gene Therapy for Retinal DegenerationR01EY021805 · NEI · TUFTS UNIVERSITY BOSTON · PI KUMAR-SINGH, RAJENDRA · 2011 to 2014
$1.8M
VP22 AND TAT mediated gene therapy for the CNSR01EY014991 · NEI · UNIVERSITY OF UTAH · PI KUMAR-SINGH, RAJENDRA · 2004 to 2009
$1.4M
NEI NIH HHS EY013887NEI NIH HHS EY014991NEI NIH HHS R01 EY013837NEI NIH HHS R01 EY014991NEI NIH HHS R01 EY021805
6 · The paper itself

Abstract

As in other organ systems, gene and drug delivery to ocular tissues such as the retina and cornea is hampered by inefficient penetration of therapeutic molecules across the plasma membrane. We describe the use of a novel peptide for ocular delivery (POD) with protein transduction properties, for delivery of small and large molecules across the plasma membrane. POD enters cells within 5 minutes in a temperature dependent manner. POD can compact and deliver plasmid DNA, achieving transgene expression in >50% of human embryonic retinoblasts. Delivery of small interfering RNA (siRNA) duplexes to cells using POD, allowed for silencing of transgene expression by >50%. POD could also be used to deliver quantum dots in vitro and in vivo. Upon ocular delivery, POD rapidly entered neural retina and localized to retinal pigment epithelium (RPE), photoreceptor, and ganglion cells. Additionally, POD was able to enter corneal epithelium, sclera, choroid, and the dura of the optic nerve via topical application. POD also functions as a bacteriostatic, a useful property for a carrier of molecules to post mitotic neural ocular tissues.

Indexed as

Cell Membrane PermeabilityDrug Delivery SystemsAmino Acid SequenceCell LineCorneaCorneal DiseasesDrug CarriersHumansMolecular Sequence DataPeptidesPlasmidsRetinaRNA, Small InterferingDrug CarriersPeptidesRNA, Small Interfering

Identifiers

PMID17923842
PMCPMC4145720
OpenAlexW2158617708

What OpenQuestion holds

Textmetadata
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.