Silica
nanoparticles (SiNPs) are produced on an industrial scale
and used in various fields including health care, because silica is
stable, inexpensive, and easy to handle. Despite these benefits, there
is concern that exposure to SiNPs may lead to adverse effects in certain
types of cells or tissues, such as hemolysis, immune responses, and
developmental abnormalities in the brain and developing embryos. Although
investigations on the toxicity of SiNPs against neurons are essential
for medicinal use, only a few studies have assessed the direct effects
of SiNPs on cells derived from the central nervous system. In this
study, we investigated the toxic effects of SiNPs on primary cultures
of hippocampal cells, using SiNPs with diameters of 10–1500
nm. We showed that treatment with SiNPs caused oxidative stress and
cell death. Furthermore, we found that these cytotoxicities were dependent
on the particle size, concentration, and surface charge of SiNPs,
as well as the treatment temperature. The toxicity was reduced by
SiNP surface functionalization or protein coating and by pretreating
cells with an antioxidant, suggesting that contact-induced oxidative
stress may be partially responsible for SiNP-induced cell death. These
data will be valuable for utilizing SiNPs in biomedical applications.