Journal
NANOMATERIALS
Volume 11, Issue 7, Pages -Publisher
MDPI
DOI: 10.3390/nano11071702
Keywords
gold nanoparticles; rats; pharmacokinetics; biodistribution; histopathology; clinical chemistry; hematology
Categories
Funding
- European Union's Horizon 2020 research and innovation program [857381]
- project VISION (Strategies to strengthen scientific excellence and innovation capacity for early diagnosis of gastrointestinal cancers)
- project HISENTS [685817]
- VEGA [2/0055/20, 2/0121/21]
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The study demonstrates potential toxic effects of tissue accumulation of PEG-AuNPs, primarily manifesting as cellular changes in the liver and spleen, but with unclear long-term effects.
Despite the obvious advantages of gold nanoparticles for biomedical applications, controversial and incomplete toxicological data hamper their widespread use. Here, we present the results from an in vivo toxicity study using gold nanoparticles coated with polyethylene glycol (PEG-AuNPs). The pharmacokinetics and biodistribution of PEG-AuNPs were examined in the rat's liver, lung, spleen, and kidney after a single i.v. injection (0.7 mg/kg) at different time intervals. PEG-AuNPs had a relatively long blood circulation time and accumulated primarily in the liver and spleen, where they remained for up to 28 days after administration. Increased cytoplasmic vacuolation in hepatocytes 24 h and 7 days after PEG-AuNPs exposure and apoptotic-like cells in white splenic pulp 24 h after administration has been detected, however, 28 days post-exposure were no longer observed. In contrast, at this time point, we identified significant changes in lipid metabolism, altered levels of liver injury markers, and elevated monocyte count, but without marked biological relevance. In blood cells, no DNA damage was present in any of the studied time intervals, with the exception of DNA breakage transiently detected in primary kidney cells 4 h post-injection. Our results indicate that the tissue accumulation of PEG-AuNPs might result in late toxic effects.
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