Journal
TOXICOLOGICAL SCIENCES
Volume 136, Issue 1, Pages 120-130Publisher
OXFORD UNIV PRESS
DOI: 10.1093/toxsci/kft187
Keywords
zinc oxide nanoparticles; sunscreen; dissolution; Zn-2#x002B; nanotoxicity
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Funding
- National Health and Medical Research Council (Australia) [616621]
- Advanced Manufacturing Cooperative Research Centre (AMCRC) [1.1.1]
- Victorian Centre for Advanced Materials Manufacturing Ltd (VCAMM)
- Micronisers Australasia Pty Ltd
- Baxter Laboratories Pty Ltd.
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Although zinc oxide (ZnO) nanoparticles (NPs) have been widely formulated in sunscreens, the relationship between reactive oxygen species (ROS) generation induced by these particles, zinc ions, and cytotoxicity is not clearly understood. This study explores whether these factors can be accurately quantified and related. The study demonstrates a strong correlation between ZnO NPinduced cytotoxicity and free intracellular zinc concentration (R-2 .945) in human immune cells, indicating a requirement for NP dissolution to precede cytotoxicity. In addition, although direct exposure to ZnO NPs was found to induce cytotoxicity at relatively high concentrations, indirect exposure (via dialysis) was not cytotoxic, even at extremely high concentrations, highlighting a requirement for NP-to-cell contact. Elevated levels of ROS present in NP-exposed cells also correlated to both cytotoxicity and intracellular free zinc. Although the addition of antioxidant was able to reduce ROS, cytotoxicity to ZnO NPs was unaffected, suggesting ROS may be, in part, a result of cytotoxicity rather than a causal factor. This study highlights both the requirement and role of intracellular dissolution of zinc nanomaterials to elicit a cytotoxic response. This response is only partially ROS dependent, and therefore, modification of NP uptake and their intracellular solubility are key components in modulating the bioactivity of ZnO NPs.
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