Evidence map›Paper›PMID 24008224›Full record

ArticleNanotechnology2013

Chitosan coating of copper nanoparticles reduces in vitro toxicity and increases inflammation in the lung.

Kristan L S Worthington, Andrea Adamcakova-Dodd, Amaraporn Wongrakpanich, Imali A Mudunkotuwa, Kranti A Mapuskar, Vijaya B Joshi, C Allan Guymon, Douglas R Spitz, Vicki H Grassian, Peter S Thorne and 1 more

Abstract read
In one paragraph

Article in Nanotechnology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
  2. Article
  3. Lung inflammation perturbation by engineered nanoparticles.Frontiers in bioengineering and biotechnology · 2023
    Review
  4. Journal of hazardous materials advances · 2022
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Effects of nano-copper on maize yield and inflammatory response in mice.Iranian journal of basic medical sciences · 2019
    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

11 authors at 1 institution in 1 country.

Kristan L S WorthingtonDepartment of Chemical and Biochemical Engineering, College of Engineering, University of Iowa, Iowa City, IA 52242, USA. Department of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy, University of Iowa, Iowa City, IA 52242, USA.
Andrea Adamcakova-Dodd
Amaraporn Wongrakpanich
Imali A Mudunkotuwa
Kranti A Mapuskar
Vijaya B Joshi
C Allan Guymon
Douglas R Spitz
Vicki H Grassian
Peter S Thorne
Aliasger K Salem
University of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Brandi Janssen · 1990 to 2026
$40.5M
Chitosan-plasmid DNA nanoplexes and adenoviruses as prostate cancer vaccinesR21CA133456 · NCI · UNIVERSITY OF IOWA · PI SALEM, ALIASGER K · 2008 to 2009
$338k
Engineered Optimal Adjuvant and Antigen Release from Biodegradable NanoparticlesR21CA128414 · NCI · UNIVERSITY OF IOWA · PI SALEM, ALIASGER K · 2009 to 2010
$264k
NCI NIH HHS 1R21CA128414-01A2/UINCI NIH HHS 1R21CA13345-01NCI NIH HHS P30 CA086862NCI NIH HHS P30CA086862NCI NIH HHS R21 CA128414NCI NIH HHS R21 CA133456NIEHS NIH HHS P30 ES005605NIEHS NIH HHS P30ES005605
6 · The paper itself

Abstract

Despite their potential for a variety of applications, copper nanoparticles induce very strong inflammatory responses and cellular toxicity following aerosolized delivery. Coating metallic nanoparticles with polysaccharides, such as biocompatible and antimicrobial chitosan, has the potential to reduce this toxicity. In this study, copper nanoparticles were coated with chitosan using a newly developed and facile method. The presence of coating was confirmed using x-ray photoelectron spectroscopy, rhodamine tagging of chitosan followed by confocal fluorescence imaging of coated particles and observed increases in particle size and zeta potential. Further physical and chemical characteristics were evaluated using dissolution and x-ray diffraction studies. The chitosan coating was shown to significantly reduce the toxicity of copper nanoparticles after 24 and 52 h and the generation of reactive oxygen species as assayed by DHE oxidation after 24 h in vitro. Conversely, inflammatory response, measured using the number of white blood cells, total protein, and cytokines/chemokines in the bronchoalveolar fluid of mice exposed to chitosan coated versus uncoated copper nanoparticles, was shown to increase, as was the concentration of copper ions. These results suggest that coating metal nanoparticles with mucoadhesive polysaccharides (e.g. chitosan) could increase their potential for use in controlled release of copper ions to cells, but will result in a higher inflammatory response if administered via the lung.

Indexed as

Metal NanoparticlesAdministration, IntranasalAnimalsBronchoalveolar Lavage FluidCell LineCell SurvivalChitosanCopperCytokinesHumansLungMaleMiceMice, Inbred C57BLPneumoniaChitosanCopperCytokines

Identifiers

PMID24008224
PMCPMC3816956
OpenAlexW2066739757

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.