Evidence map›Paper›PMID 22365809›Full record

ArticleBiomaterials2012

Polyethyleneimine-lipid conjugate-based pH-sensitive micellar carrier for gene delivery.

Rupa R Sawant, Shravan Kumar Sriraman, Gemma Navarro, Swati Biswas, Riddhi A Dalvi, Vladimir P Torchilin

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 116 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Lipid-based regulators of immunity.Bioengineering & translational medicine · 2022
    Review
  8. Review
  9. Article
  10. Cytotoxicity of Novel Redox Sensitive PEGPharmaceutical research · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Radiofrequency ablation (RFA)-induced systemic tumor growth can be reduced by suppression of resultant heat shock proteins.International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2018
    Article
  16. Article
  17. Review
  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

6 authors at 1 institution in 1 country.

Rupa R SawantCenter for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA 02115, USA.
Shravan Kumar Sriraman
Gemma Navarro
Swati Biswas
Riddhi A Dalvi
Vladimir P Torchilin
Northeastern University · US

Funding

Physico-Chemical Nanocharacterization CoreU54CA151881 · NCI · NORTHEASTERN UNIVERSITY · PI SRIDHAR, SRINIVAS · 2010 to 2014
$12.4M
MULTIFUNCTIONAL STIMULI-SENSITIVE PHARMACEUTICAL NANOCARRIERSR01CA121838 · NCI · NORTHEASTERN UNIVERSITY · PI TORCHILIN, VLADIMIR P · 2006 to 2010
$1.4M
NCI NIH HHS 1U54CA151881NCI NIH HHS R01 CA121838NCI NIH HHS R01CA121838NCI NIH HHS U54 CA151881
6 · The paper itself

Abstract

A low molecular weight polyethyleneimine (PEI 1.8 kDa) was modified with dioleoylphosphatidylethanolamine (PE) to form the PEI-PE conjugate investigated as a transfection vector. The optimized PEI-PE/pDNA complexes at an N/P ratio of 16 had a particle size of 225 nm, a surface charge of +31 mV, and protected the pDNA from the action of DNase I. The PEI-PE conjugate had a critical micelle concentration (CMC) of about 34 μg/ml and exhibited no toxicity compared to a high molecular weight PEI (PEI 25 kDa) as tested with B16-F10 melanoma cells. The B16-F10 cells transfected with PEI-PE/pEGFP complexes showed protein expression levels higher than with PEI-1.8 or PEI-25 vectors. Complexes prepared with YOYO 1-labeled pEGFP confirmed the enhanced delivery of the plasmid with PEI-PE compared to PEI-1.8 and PEI-25. The PEI-PE/pDNA complexes were also mixed with various amounts of micelle-forming material, polyethylene glycol (PEG)-PE to improve biocompatibility. The resulting particles exhibited a neutral surface charge, resistance to salt-induced aggregation, and good transfection activity in the presence of serum in complete media. The use of the low-pH-degradable PEG-hydrazone-PE produced particles with transfection activity sensitive to changes in pH consistent with the relatively acidic tumor environment.

Indexed as

Gene Transfer TechniquesMicellesAnimalsCell DeathChromatography, High Pressure LiquidDNAElectrophoresis, Agar GelHydrogen-Ion ConcentrationLipidsMelanoma, ExperimentalMiceMicroscopy, ConfocalParticle SizePhosphatidylethanolaminesPolyethylene GlycolsPolyethyleneiminedioleoyl phosphatidylethanolamineDNALipidsMicellesPhosphatidylethanolaminesPolyethylene GlycolsPolyethyleneimine

Identifiers

PMID22365809
PMCPMC3527089
OpenAlexW2116162518

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.