Evidence map›Paper›PMID 23928214›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2014

Phospholipid-modified polyethylenimine-based nanopreparations for siRNA-mediated gene silencing: implications for transfection and the role of lipid components.

Gemma Navarro, Sean Essex, Rupa R Sawant, Swati Biswas, Dattatri Nagesha, Srinivas Sridhar, Conchita Tros de ILarduya, Vladimir P Torchilin

Abstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 44 citations in OpenAlex.

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  14. Hypoxia-targeted siRNA delivery.Angewandte Chemie (International ed. in English) · 2014
    Article
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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

8 authors at 2 institutions in 2 countries.

Gemma NavarroCenter for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, USA.
Sean EssexCenter for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, USA.
Rupa R SawantCenter for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, USA.
Swati BiswasDepartment of Pharmacy, Birla Institute of Technology and Sciences-Pilani., Hyderabad Campus Jawahar Nagar, Shameerpet Mandal. Hyderabad-500078. AP., India.
Dattatri NageshaDepartment of Pharmaceutics, JSS College of Pharmacy, JSS University S. S. Nagar, Mysore 570 015.
Srinivas SridharElectronic Materials Research Institute, Northeastern University, Boston, MA, USA.
Conchita Tros de ILarduyaDepartment of Pharmacy and Pharmaceutical Technology, School of Pharmacy, University of Navarra, Pamplona, Spain.
Vladimir P TorchilinCenter for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, USA. Electronic address: v.torchilin@neu.edu.
Northeastern University · USUniversidad de Navarra · ES

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

The clinical application of gene silencing mediated by small interfering RNA (siRNA) has been limited by the lack of efficient and safe carriers. Phospholipid modification of low molecular weight polyethylenimine (PEI 1.8 kDa) dramatically increased its gene down-regulation capacity while keeping cytotoxicity levels low. The silencing efficacy was highly dependent on the nature of the lipid grafted to PEI and the polymer/siRNA ratio employed. Phosphoethanolamine (DOPE and DPPE) and phosphocholine (PC) conjugation did not change the physicochemical properties and siRNA binding capacity of PEI complexes but had a large impact on their transfection and ability to down-regulate Green Fluorescent Protein (GFP) expression (60%, 30% and 5% decrease of GFP expression respectively). We found that the micelle-forming structure of DOPE and DPPE-PEI dramatically changed PEI's interaction with cell membranes and played a key role in promoting PEI 1.8 kDa transfection, completely ineffective in the absence of the lipid modification. FROM THE CLINICAL EDITOR: While siRNA-based gene silencing methods could have numerous clinical applications, efficient delivery remains a major challenge. This team reports that DOPE-PEI and DPPE-PEI based micelle-forming nanostructures may be able to provide an efficient vector for siRNA transfection.

Indexed as

RNA InterferenceAnimalsCell LineCell MembraneDrug CarriersEthanolaminesGreen Fluorescent ProteinsHumansInhibitory Concentration 50LipidsMiceMicellesMolecular WeightNanomedicineNanoparticlesPhospholipidsDrug CarriersEthanolaminesGreen Fluorescent ProteinsLipidsMicellesPhospholipidsPhosphorylcholinephosphorylethanolaminePolyethyleneimineRNA, Small InterferingLipid conjugationMicellePhospholipidPolyethylenimineRNA interferencesiRNA delivery

Identifiers

PMID23928214
PMCPMC3916950
OpenAlexW2154506031

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.