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Synthesis of spherical and rods-like titanium oxide nanoparticles (TiO NPs) and evaluation of their cytotoxicity towards colon cells in vitro. | LitMetric

Synthesis of spherical and rods-like titanium oxide nanoparticles (TiO NPs) and evaluation of their cytotoxicity towards colon cells in vitro.

Biochim Biophys Acta Gen Subj

Institute of Nuclear Physics Polish Academy of Sciences, 31-342 Krakow, Poland; Department of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, 20-093, Poland.

Published: December 2024

AI Article Synopsis

  • Titanium oxide nanoparticles (TiO NPs) are found in medicines and sunscreens but have been shown to negatively affect colon cells, prompting a study on their properties and cytotoxicity.
  • The research involved synthesizing spherical (TiO NSs) and rod-like (TiO NRs) nanoparticles, which were characterized using various microscopy techniques to confirm their sizes and crystalline phases.
  • Cytotoxicity tests revealed harmful effects on both normal colon cells and cancerous cells at higher concentrations, with nanoparticles inducing the generation of reactive oxygen species, suggesting potential for biomedical applications despite the risks.

Article Abstract

Titanium oxide nanoparticles (TiO NPs) are currently used as ingredients in medicines and sunscreens. Unfortunately, recent information about TiO NPs indicates their undesirable biological effect on colon cells. Therefore, the aim of this work was to synthesize and evaluate the physicochemical characterization of spherical (TiO NSs) and rods-like (TiO NRs) NPs, followed by assessment their cytotoxicity. For this purpose, both normal colon epithelial cells (CRL-1790) and cancerous colon cells (SW480) were used. Scanning transmission electron microscopy (STEM) showed that TiO NSs with a diameter of ≈10 nm and TiO NRs with the size of the longer axis ≈25 nm and shorter axis ≈3 nm were obtained. Based on the selected area electron diffraction (SAED) patterns, it was found that crystalline phases were obtained for both TiO NPs. The UV-Vis spectra showed no contamination of TiO NPs. Zeta potential values were 9.7 mV and 3.1 mV for NSs and NRs, respectively. Cytotoxicity of TiO NPs was assessed using the MTS (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxy-methoxy-phenyl)-2-(4-sulfophenyl)-2H-tetrazolium) test for various concentration of NPs. The cytotoxic effect for both TiO NPs was visible for concentration of 75 μg/ml (for CRL-1790) and 50 μg/ml (for SW480) and higher, and it did not depend on the shape. Moreover, both types of TiO NPs (in higher concentration) induce the generation of reactive oxygen species (ROS) in cells cultured with these NPs. Holotomographic microscopy studies showed increased cellular uptake of TiO NPs by SW480. The obtained results for the synthesized TiO NPs are a promising prospect for their use in biomedical application.

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Source
http://dx.doi.org/10.1016/j.bbagen.2024.130743DOI Listing

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