Evidence map›Paper›PMID 23453959›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2013

PEGylation of cationic, shell-crosslinked-knedel-like nanoparticles modulates inflammation and enhances cellular uptake in the lung.

Aida Ibricevic, Sean P Guntsen, Ke Zhang, Ritu Shrestha, Yongjian Liu, Jing Yi Sun, Michael J Welch, Karen L Wooley, Steven L Brody

Abstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Review
  2. Lung inflammation perturbation by engineered nanoparticles.Frontiers in bioengineering and biotechnology · 2023
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Polymeric nanoparticles in development for treatment of pulmonary infectious diseases.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2016
    Review
  11. Article
  12. Nanotechnology in respiratory medicine.Respiratory research · 2015
    Review
  13. Visualization of pulmonary clearance mechanisms via noninvasive optical imaging validated by near-infrared flow cytometry.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2015
    Article
  14. Article
  15. Article
  16. 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

9 authors.

Aida IbricevicDepartment of Internal Medicine, Washington University, St. Louis, Missouri, USA.
Sean P Guntsen
Ke Zhang
Ritu Shrestha
Yongjian Liu
Jing Yi Sun
Michael J Welch
Karen L Wooley
Steven L Brody

Funding

NHLBI NIH HHS HHSN268201000046C
6 · The paper itself

Abstract

The airway provides a direct route for administration of nanoparticles bearing therapeutic or diagnostic payloads to the lung, however optimization of nanoplatforms for intracellular delivery remains challenging. Poly(ethylene glycol) (PEG) surface modification improves systemic performance but less is known about PEGylated nanoparticles administered to the airway. To test this, we generated a library of cationic, shell crosslinked knedel-like nanoparticles (cSCKs), including PEG (1.5 kDa PEG; 2, 5, 10 molecules/polymer arm) on the outer shell. Delivery of PEGylated cSCK to the mouse airway showed significantly less inflammation in a PEG dose-dependent manner. PEGylation also enhanced the entry of cSCKs in lung alveolar epithelial cells and improved surfactant penetration. The PEGylation effect could be explained by the altered mechanism of endocytosis. While non-PEGylated cSCKs used the clathrin-dependent route for endocytosis, entry of PEGylated cSCK was clathrin-independent. Thus, nanoparticle surface modification with PEG represents an advantageous design for lung delivery. FROM THE CLINICAL EDITOR: In this study, the effects of PEGylation were studied on cross linked knedel-like nanoparticles in drug delivery through the lungs, demonstrating less airway inflammation in the studied model than with non-PEGylated nanoparticles, which suggests an overall favorable profile of PEGylated nanoparticles for alveolar delivery.

Indexed as

EndocytosisAlveolar Epithelial CellsAnimalsCationsCell LineCross-Linking ReagentsDrug Delivery SystemsInflammationIntracellular SpaceLungMiceMice, Inbred C57BLNanoparticlesPolyethylene GlycolsCationsCross-Linking ReagentsPolyethylene GlycolsAirwayAlveolar epithelial cellsBALbronchoalveolar lavagecationic shell crosslinked knedel-likechlorpromazineCPMcSCKMacrophageMDCmethyl-β-cyclodextranmonodansylcadaverineMβCDnanoparticleNPPEGpoly(ethylene glycol)Poly(ethylene glycol)SDstandard deviationSurfactant

Identifiers

PMID23453959
PMCPMC3724762

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Registered trials

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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.