Evidence map›Paper›PMID 18929605›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2009

Self-assembling micelle-like nanoparticles based on phospholipid-polyethyleneimine conjugates for systemic gene delivery.

Young Tag Ko, Amit Kale, William C Hartner, Brigitte Papahadjopoulos-Sternberg, Vladimir P Torchilin

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 96 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Cell-Penetrating Peptides Delivering siRNAs: An Overview.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Applying horizontal gene transfer phenomena to enhance non-viral gene therapy.Journal of controlled release : official journal of the Controlled Release Society · 2013
    Review
  14. Article
  15. Nanomedicine for gene therapy.Drug delivery and translational research · 2013
    Article
  16. Article
  17. Article
  18. Critical evaluation of biodegradable polymers used in nanodrugs.International journal of nanomedicine · 2013
    Review
  19. Article
  20. Alkane-modified short polyethyleneimine for siRNA delivery.Journal of controlled release : official journal of the Controlled Release Society · 2012
    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

5 authors at 2 institutions in 1 country.

Young Tag KoDepartment of Pharmaceutical Sciences, Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA 02115, USA.
Amit Kale
William C Hartner
Brigitte Papahadjopoulos-Sternberg
Vladimir P Torchilin
Northeastern University · USNano Hydrophobics (United States) · US

Funding

LONG-CIRCULATING POLYMER-MODIFIED LIPOSOMESR01HL055519 · NHLBI · NORTHEASTERN UNIVERSITY · PI TORCHILIN, VLADIMIR P · 1997 to 2008
$2.0M
NHLBI NIH HHS R01 HL055519NHLBI NIH HHS R01 HL55519
6 · The paper itself

Abstract

With few exceptions, where local administration is feasible, progress towards broad clinical application of gene therapies requires the development of effective delivery systems. Here we report a novel non-viral gene delivery vector, 'micelle-like nanoparticle' (MNP) suitable for systemic application. MNP were engineered by condensing plasmid DNA with a chemical conjugate of phospholipid with polyethylenimine (PLPEI) and then coating the complexes with an envelope of lipid monolayer additionally containing polyethylene glycol-phosphatidyl ethanolamine (PEG-PE), resulting in spherical 'hard-core' nanoparticles loaded with DNA. MNP allowed for complete protection of the loaded DNA from enzymatic degradation, resistance to salt-induced aggregation, and reduced cytotoxicity. MNP also demonstrated prolonged blood circulation and low RES accumulation. Intravenous injection of MNP loaded with plasmid DNA encoding for the Green Fluorescence Protein (GFP) resulted in an effective transfection of a distal tumor. Thus, MNP provide a promising tool for systemic gene therapy.

Indexed as

Gene Transfer TechniquesAnimalsCarcinoma, Lewis LungCell Line, TumorCell SurvivalDNAGene ExpressionGreen Fluorescent ProteinsMaleMiceMice, Inbred BALB CMice, Inbred C57BLMicellesMicroscopy, ElectronMicroscopy, FluorescenceNanoparticles1-palmitoyl-2-azelaoyl-sn-glycero-3-phosphocholine1-palmitoyl-2-oleoylphosphatidylcholineDNAGreen Fluorescent ProteinsMicellesPhosphatidylcholinesPhospholipidsPhosphorylcholinePolyethyleneimine

Identifiers

PMID18929605
PMCPMC3183824
OpenAlexW2017307273

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.