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

• Published in: Nanomaterials (Basel, Switzerland) Switzerland), 2017-10, Vol.7 (10), p.307
• Main Authors: Kornberg, Tiffany G, Stueckle, Todd A, Antonini, James A, Rojanasakul, Yon, Castranova, Vincent, Yang, Yong, Wang, Liying
• Format: Article
• Language: English
• Subjects: Animal human relations; Biocompatibility; Catalysts; Cell culture; Correlation analysis; Disruption; Drug delivery; Drug delivery systems; Exposure; Fibrosis; Genotoxicity; Homeostasis; in vitro model; in vivo; In vivo methods and tests; Internalization; Iron; Iron ores; iron oxide; Iron oxides; Lung diseases; Nanoparticles; Occupational exposure; Occupational health; Oxidative stress; Particulates; Pyrite; Review; Risk; Thermoplastic resins; Toxicity
• ISSN: 2079-4991; 2079-4991
• DOI: 10.3390/nano7100307

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.