Evidence map›Paper›PMID 26287725›Full record

ArticleMolecular pharmaceutics2015

Reductively Responsive Hydrogel Nanoparticles with Uniform Size, Shape, and Tunable Composition for Systemic siRNA Delivery in Vivo.

Da Ma, Shaomin Tian, Jeremy Baryza, J Christopher Luft, Joseph M DeSimone

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-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

12 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. SiRNA Crosslinked Nanoparticles for the Treatment of Inflammation-induced Liver Injury.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2017
    Article
  9. Article
  10. The delivery of therapeutic oligonucleotides.Nucleic acids research · 2016
    Review
  11. Article
  12. Targeted endothelial nanomedicine for common acute pathological conditions.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
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 4 institutions in 1 country.

Da Ma *Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599, United States.
Shaomin Tian *Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina 27599, United States.
Jeremy BaryzaNovartis Institutes for BioMedical Research, Cambridge, Massachusetts 02139, United States.
J Christopher LuftLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina 27599, United States.
Joseph M DeSimoneDepartment of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599, United States.
UNC Lineberger Comprehensive Cancer CenterNorth Carolina State University · USNovartis (United States) · USUniversity of North Carolina at Chapel Hill · US

Funding

Delivery of Biological Therapeutics: Using Engineered Particles and Novel DeliverDP1CA174425 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DESIMONE, JOSEPH M. · 2012 to 2013
$1.4M
NCI NIH HHS DP1 CA174425
6 · The paper itself

Abstract

To achieve the great potential of siRNA based gene therapy, safe and efficient systemic delivery in vivo is essential. Here we report reductively responsive hydrogel nanoparticles with highly uniform size and shape for systemic siRNA delivery in vivo. "Blank" hydrogel nanoparticles with high aspect ratio were prepared using continuous particle fabrication based on PRINT (particle replication in nonwetting templates). Subsequently, siRNA was conjugated to "blank" nanoparticles via a disulfide linker with a high loading ratio of up to 18 wt %, followed by surface modification to enhance transfection. This fabrication process could be easily scaled up to prepare large quantity of hydrogel nanoparticles. By controlling hydrogel composition, surface modification, and siRNA loading ratio, siRNA conjugated nanoparticles were highly tunable to achieve high transfection efficiency in vitro. FVII-siRNA conjugated nanoparticles were further stabilized with surface coating for in vivo siRNA delivery to liver hepatocytes, and successful gene silencing was demonstrated at both mRNA and protein levels.

Indexed as

Drug Delivery SystemsAnimalsElectrophoresis, Agar GelHeLa CellsHumansHydrogelsMice, Inbred C57BLMicroscopy, Electron, ScanningNanoparticlesParticle SizeRNA, Small InterferingHydrogelsRNA, Small Interferingdrug deliverygene therapyhydrogelnanoparticlessiRNA

Identifiers

PMID26287725
PMCPMC4839470
OpenAlexW2426988470

What OpenQuestion holds

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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.