Abstract

Cerium oxide nanoparticles (CeO2NPs) exhibit biomedical properties as well as cytotoxic effects on tumor cells. Therefore, recent CeO2NPs have been regarded by numerous researchers as metal-based antitumor agents. Moreover, a new series of CeO2NPs having different structures and morphologies such as nickel (Ni)-doped CeO2, hollow CeO2 (hCeO2), and hollow CeO2/silicon dioxide (SiO2) (hCeO2/SiO2) NPs have been synthesized. All these compounds have been further characterized by fourier transform infrared (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive X-ray (EDX), high-resolution transmission electron microscopy (HRTEM), and Brunauer-Emmett-Teller (BET) analyses. Similarly, HRTEM analyses showed that hCeO2/SiO2 nanostructures were composed of CeO2 as core and SiO2 as shell. To this end, cytotoxic activity of synthesized NPs was investigated on HT-29, as a human colorectal cancer cell line and human foreskin fibroblast cell line (HFFF2). The hollow core/shell nanostructures indicated more cytotoxicity compared with other synthesized compounds on HT-29 cell line. The results also revealed that hCeO2/SiO2NPs had less half maximal inhibitory concentration (IC50) (18.625 µg/ml) than other synthesized compounds. All four compounds showed significantly less cytotoxicity effect in non-cancerous cells (HFFF2) compared to tumoral cells (HT-29).

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