Cytotoxicity evaluation of silica nanoparticles using fish cell lines

• Published in: In vitro cellular & developmental biology. Animal Vol. 50; no. 5; pp. 427 - 438
• Main Authors: Vo, Nguyen T. K., Bufalino, Mary R., Hartlen, Kurtis D., Kitaev, Vladimir, Lee, Lucy E. J.
• Format: Journal Article
• Language: English
• Published: Boston Springer Science + Business Media 01.05.2014; Springer US; Society for In Vitro Biology
• Subjects: Animal Genetics and Genomics; Animals; Biomedical and Life Sciences; Carassius auratus; CELL AND TISSUE MODELS; Cell Biology; Cell Culture; Cell Line - drug effects; Cell lines; Cell Survival - drug effects; Cellular metabolism; Cytotoxicity; Danio rerio; Developmental Biology; Dosage; Endothelial cells; Environmental Monitoring; Epithelial cells; Fish; Freshwater; Life Sciences; Nanoparticles; Nanoparticles - toxicity; Neurons; Oncorhynchus mykiss; Silicon Dioxide - toxicity; Stem Cells; Trout; Water Pollutants, Chemical - toxicity; Zebrafish; Alamar Blue; Fish cell lines; Silica nanoparticles; Cytotoxicity; Nanotoxicology
• ISSN: 1071-2690; 1543-706X
• DOI: 10.1007/s11626-013-9720-3

Nanoparticles (NPs) have extensive industrial, biotechnological, and biomedical/pharmaceutical applications, leading to concerns over health risks to humans and biota. Among various types of nanoparticles, silica nanoparticles (SiO2 NPs) have become popular as nanostructuring, drug delivery, and optical imaging agents. SiO2 NPs are highly stable and could bioaccumulate in the environment. Although toxicity studies of SiO2 NPs to human and mammalian cells have been reported, their effects on aquatic biota, especially fish, have not been significantly studied. Twelve adherent fish cell lines derived from six species (rainbow trout, fathead minnow, zebrafish, goldfish, haddock, and American eel) were used to comparatively evaluate viability of cells by measuring metabolic impairment using Alamar Blue. Toxicity of SiO2 NPs appeared to be size-, time-, temperature-, and dose-dependent as well as tissue-specific. However, dosages greater than 100 μg/mL were needed to achieve 24 h EC50 values (effective concentrations needed to reduce cell viability by 50%). Smaller SiO2 NPs (16 nm) were relatively more toxic than larger sized ones (24 and 44 nm) and external lining epithelial tissue (skin, gills)-derived cells were more sensitive than cells derived from internal tissues (liver, brain, intestine, gonads) or embryos. Higher EC50 values were achieved when toxicity assessment was performed at higher incubation temperatures. These findings are in overall agreement with similar human and mouse cell studies reported to date. Thus, fish cell lines could be valuable for screening emerging contaminants in aquatic environments including NPs through rapid high-throughput cytotoxicity bioassays.