Evidence map›Paper›PMID 25575782›Full record

ArticleToxicology in vitro : an international journal published in association with BIBRA2015

Toxicity of copper oxide nanoparticles in lung epithelial cells exposed at the air-liquid interface compared with in vivo assessment.

Xuefang Jing, Jae Hong Park, Thomas M Peters, Peter S Thorne

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Toxicology in vitro : an international journal published in association with BIBRA, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.8field-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

47 citing papers in PubMed, 116 citations in OpenAlex.

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  14. Predicting nanomaterials pulmonary toxicity in animals by cell culture models: Achievements and perspectives.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2022
    Review
  15. Article
  16. Developing Benign Ni/g-CIndustrial & engineering chemistry research · 2022
    Article
  17. Article
  18. Article
  19. Polyphenol effects on CuO-nanoparticle-mediated DNA damage, reactive oxygen species generation, and fibroblast cell death.Toxicology in vitro : an international journal published in association with BIBRA · 2022
    Article
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Xuefang JingDepartment of Occupational and Environmental Health, University of Iowa, Iowa City, IA 52242, USA. Electronic address: xuefang-jing@uiowa.edu.
Jae Hong ParkDepartment of Occupational and Environmental Health, University of Iowa, Iowa City, IA 52242, USA. Electronic address: jaehong-park@uiowa.edu.
Thomas M PetersDepartment of Occupational and Environmental Health, University of Iowa, Iowa City, IA 52242, USA. Electronic address: thomas-m-peters@uiowa.edu.
Peter S ThorneDepartment of Occupational and Environmental Health, University of Iowa, Iowa City, IA 52242, USA. Electronic address: peter-thorne@uiowa.edu.
University of Iowa · US

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Brandi Janssen · 1990 to 2026
$40.5M
Vector Core-Core 2P30DK054759 · NIDDK · UNIVERSITY OF IOWA · PI Alejandro Antonio Pezzulo · 1998 to 2026
$30.5M
NIDDK NIH HHS P30 DK054759NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

The toxicity of spark-generated copper oxide nanoparticles (CuONPs) was evaluated in human bronchial epithelial cells (HBEC) and lung adenocarcinoma cells (A549 cells) using an in vitro air-liquid interface (ALI) exposure system. Dose-response results were compared to in vivo inhalation and instillation studies of CuONPs. Cells were exposed to filtered, particle-free clean air (controls) or spark-generated CuONPs. The number median diameter, geometric standard deviation and total number concentration of CuONPs were 9.2 nm, 1.48 and 2.27×10(7)particles/cm(3), respectively. Outcome measures included cell viability, cytotoxicity, oxidative stress and proinflammatory chemokine production. Exposure to clean air (2 or 4h) did not induce toxicity in HBEC or A549 cells. Compared with controls, CuONP exposures significantly reduced cell viability, increased lactate dehydrogenase (LDH) release and elevated levels of reactive oxygen species (ROS) and IL-8 in a dose-dependent manner. A549 cells were significantly more susceptible to CuONP effects than HBEC. Antioxidant treatment reduced CuONP-induced cytotoxicity. When dose was expressed per area of exposed epithelium there was good agreement of toxicity measures with murine in vivo studies. This demonstrates that in vitro ALI studies can provide meaningful data on nanotoxicity of metal oxides.

Indexed as

AntioxidantsCell Line, TumorCell MembraneCell SurvivalChemokinesCopperDose-Response Relationship, DrugEpithelial CellsHumansLungNanoparticlesOxidative StressParticle SizeAntioxidantsChemokinesCoppercuprous oxideAir–liquid interfaceCopper oxide nanoparticlesHuman bronchial epithelial cellsIn vitro exposureN-acetylcysteineOxidative stress

Identifiers

PMID25575782
PMCPMC4373347
OpenAlexW2079499842

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.