Evidence map›Paper›PMID 20824309›Full record

ArticlePharmaceutical research2010

Pulmonary gene silencing in transgenic EGFP mice using aerosolised chitosan/siRNA nanoparticles.

Ebbe J B Nielsen, Jan M Nielsen, Daniel Becker, Alexander Karlas, Hridayesh Prakash, Sys Z Glud, Jonathan Merrison, Flemming Besenbacher, Thomas F Meyer, Jørgen Kjems and 1 more

Abstract read
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In one paragraph

Article in Pharmaceutical research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. RNAi therapeutic strategies for acute respiratory distress syndrome.Translational research : the journal of laboratory and clinical medicine · 2019
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. siRNA delivery to the lung: what's new?Advanced drug delivery reviews · 2014
    Review
  15. Chitosans for delivery of nucleic acids.Advanced drug delivery reviews · 2013
    Review
  16. Article
  17. Article
  18. RNAi Therapeutic Platforms for Lung Diseases.Pharmaceuticals (Basel, Switzerland) · 2013
    Article
  19. Clinical translation of RNAi-based treatments for respiratory diseases.Drug delivery and translational research · 2013
    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

11 authors at 3 institutions in 2 countries.

Ebbe J B NielsenInterdisciplinary Nanoscience Center (iNANO), University of Aarhus, Aarhus, Denmark.
Jan M Nielsen
Daniel Becker
Alexander Karlas
Hridayesh Prakash
Sys Z Glud
Jonathan Merrison
Flemming Besenbacher
Thomas F Meyer
Jørgen Kjems
Kenneth A Howard
Aarhus University · DKMax Planck Institute for Infection Biology · DEAarhus University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis work describes the production and application of an aerosolised formulation of chitosan nanoparticles for improved pulmonary siRNA delivery and gene silencing in mice.

methodsAerosolised chitosan/siRNA nanoparticles were pneumatically formed using a nebulising catheter and sized by laser diffraction. In vitro silencing of aerosolised and non-aerosolised formulations was evaluated in an EGFP endogenous-expressing H1299 cell line by flow cytometry. Non-invasive intratracheal insertion of the catheter was used to study nanoparticle deposition by histological detection of Cy3-labeled siRNA and gene silencing in transgenic EGFP mouse lungs using a flow cytometric method.

resultsFlow cytometric analysis demonstrated minimal alteration in gene silencing efficiency before (68%) and after (62%) aerosolisation in EGFP-expressing H1299 cells. Intratracheal catheter administration in mice resulted in nanoparticle deposition throughout the entire lung in both alveoli and bronchiolar regions using low amounts of siRNA. Transgenic EGFP mice dosed with the aerosolised nanoparticle formulation showed significant EGFP gene silencing (68% reduction compared to mismatch group).

conclusionsThis work provides a technology platform for effective pulmonary delivery and gene silencing of RNAi therapeutics with potential use in preclinical studies of respiratory disease treatment.

Indexed as

ChitosanGene SilencingAerosolsAnimalsBase SequenceCell LineFlow CytometryGene Knockdown TechniquesGreen Fluorescent ProteinsMiceMice, Inbred C57BLMice, TransgenicRNA InterferenceAerosolsChitosanenhanced green fluorescent proteinGreen Fluorescent Proteins

Identifiers

PMID20824309
OpenAlexW2004356674

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.