Evidence map›Paper›PMID 28984829›Full record

ReviewNanomaterials (Basel, Switzerland)2017

Potential Toxicity and Underlying Mechanisms Associated with Pulmonary Exposure to Iron Oxide Nanoparticles: Conflicting Literature and Unclear Risk.

Tiffany G Kornberg, Todd A Stueckle, James A Antonini, Yon Rojanasakul, Vincent Castranova, Yong Yang, Liying Wang

Open access · goldAbstract readReview
In one paragraph

Review in Nanomaterials (Basel, Switzerland), 2017. 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
3.7field-weighted citation impact, top 6% 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, 83 citations in OpenAlex.

  1. Article
  2. Article
  3. Cardiovascular Toxicity of Metal-Based Nanoparticles.International journal of molecular sciences · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Effects of carnosine on the embryonic development and TiOFrontiers in veterinary science · 2023
    Article
  9. Article
  10. Article
  11. Micro- and Nanosized Substances Cause Different Autophagy-Related Responses.International journal of molecular sciences · 2021
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Cytotoxicity studies of FeRoyal Society open science · 2020
    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

7 authors at 3 institutions in 1 country.

Tiffany G KornbergPharmaceutical and Pharmacological Sciences, West Virginia University, Morgantown, WV 26505, USA. tkornberg@cdc.gov.
Todd A StueckleHealth Effects Laboratory Division National Institute for Occupational Safety and Health, Morgantown, WV 26505, USA. jux5@cdc.gov.ORCID 0000-0002-2495-7443
James A AntoniniHealth Effects Laboratory Division National Institute for Occupational Safety and Health, Morgantown, WV 26505, USA. jga6@cdc.gov.
Yon RojanasakulPharmaceutical and Pharmacological Sciences, West Virginia University, Morgantown, WV 26505, USA. yrojan@hsc.wvu.edu.
Vincent CastranovaPharmaceutical and Pharmacological Sciences, West Virginia University, Morgantown, WV 26505, USA. vcastran@hsc.wvu.edu.
Yong YangDepartment of Biomedical Engineering, University of North Texas, Denton, TX 76207, USA. yong.yang@unt.edu.ORCID 0000-0003-4305-8029
Liying WangPharmaceutical and Pharmacological Sciences, West Virginia University, Morgantown, WV 26505, USA. lmw6@cdc.gov.
West Virginia University · USNational Institute for Occupational Safety and Health · USUniversity of North Texas · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fine/micron-sized iron oxide particulates are incidentally released from a number of industrial processes, including iron ore mining, steel processing, welding, and pyrite production. Some research suggests that occupational exposure to these particulates is linked to an increased risk of adverse respiratory outcomes, whereas other studies suggest that iron oxide is biologically benign. Iron oxide nanoparticles (IONPs), which are less than 100 nm in diameter, have recently surged in use as components of novel drug delivery systems, unique imaging protocols, as environmental catalysts, and for incorporation into thermoplastics. However, the adverse outcomes associated with occupational exposure to IONPs remain relatively unknown. Relevant in vivo studies suggest that pulmonary exposure to IONPs may induce inflammation, pulmonary fibrosis, genotoxicity, and extra-pulmonary effects. This correlates well with in vitro studies that utilize relevant dose, cell type(s), and meaningful end points. A majority of these adverse outcomes are attributed to increased oxidative stress, most likely caused by particle internalization, dissolution, release of free iron ions, and disruption of iron homeostasis. However, because the overall toxicity profile of IONPs is not well understood, it is difficult to set safe exposure limit recommendations that would be adequate for the protection of at-risk workers. This review article will focus on known risks following IONPs exposure supported by human, animal, and cell culture-based studies, the potential challenges intrinsic to IONPs toxicity assessment, and how these may contribute to the poorly characterized IONPs toxicity profile.

Indexed as

in vitro modelin vivoiron oxidenanoparticlestoxicity

Identifiers

PMID28984829
PMCPMC5666472
OpenAlexW2762019095

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.