In vitro cytotoxicity of SiO2 or ZnO nanoparticles with different sizes and surface charges on U373MG human glioblastoma cells

• Published in: International journal of nanomedicine Vol. 9 Suppl 2; no. 2; pp. 235 - 241
• Main Authors: Kim, Jung-Eun, Kim, Hyejin, An, Seong Soo A, Maeng, Eun Ho, Kim, Meyoung-Kon, Song, Yoon-Jae
• Format: Journal Article
• Language: English
• Published: New Zealand Dove Medical Press 15.12.2014
• Subjects: Cell Line, Tumor; Cell Survival - drug effects; Glioblastoma; Humans; Metal Nanoparticles - chemistry; Metal Nanoparticles - toxicity; Original Research; Silicon Dioxide - chemistry; Silicon Dioxide - toxicity; Zinc Oxide - chemistry; Zinc Oxide - toxicity; apoptosis
• ISSN: 1178-2013; 1176-9114; 1178-2013
• DOI: 10.2147/IJN.S57936

Silicon dioxide (SiO2) and zinc oxide (ZnO) nanoparticles are widely used in various applications, raising issues regarding the possible adverse effects of these metal oxide nanoparticles on human cells. In this study, we determined the cytotoxic effects of differently charged SiO2 and ZnO nanoparticles, with mean sizes of either 100 or 20 nm, on the U373MG human glioblastoma cell line. The overall cytotoxicity of ZnO nanoparticles against U373MG cells was significantly higher than that of SiO2 nanoparticles. Neither the size nor the surface charge of the ZnO nanoparticles affected their cytotoxicity against U373MG cells. The 20 nm SiO2 nanoparticles were more toxic than the 100 nm nanoparticles against U373MG cells, but the surface charge had little or no effect on their cytotoxicity. Both SiO2 and ZnO nanoparticles activated caspase-3 and induced DNA fragmentation in U373MG cells, suggesting the induction of apoptosis. Thus, SiO2 and ZnO nanoparticles appear to exert cytotoxic effects against U373MG cells, possibly via apoptosis.