Cytotoxicity of Zirconium Oxide Nanoparticles on Rabbit Tooth Gum Cells

Author:

Mossavi Seyed Arash Javad1,Ramandi Javad F.2,Ghanbary Fatemeh3ORCID,Hosseini Nasrin4ORCID,Naserzadeh Parvaneh5ORCID,Akhshik Masoud67ORCID,Tay Franklin R.89ORCID,Ashtari Behnaz1011ORCID

Affiliation:

1. Air Pollution Research Center, Iran University of Medical Sciences, Tehran, Iran

2. Iranian Research Organization for Science and Technology, Tehran, Iran

3. Department of Chemistry, Islamic Azad University, Mahabad Branch, Mahabad, Iran

4. Neuroscience Research Center, Iran University of Medical Sciences, Tehran, Iran

5. Endocrine Research Center, Institute of Endocrinology and Metabolism, Iran University of Medical Sciences, Tehran, Iran

6. Department of Biology, University of Toronto, Mississauga, ON, L5L 1C6, Canada

7. Fanshawe College Center for Research and Innovation, 1001 Fanshawe College Blvd., London, ON, N5Y 5R6, Canada

8. The Graduate School, Augusta University, Augusta, GA 30912, USA

9. The Dental College of Georgia, Augusta University, Augusta, Georgia

10. Radiation Biology Research Center, Iran University of Medical Sciences, Tehran, Iran

11. Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Science. Tehran, Iran

Abstract

The cytotoxicity mechanism of zirconium oxide nanoparticles (ZrO2-NPs) has not been clarified to-date. Nevertheless, the generation of reactive oxygen species (ROS) by ZrO2-NPs has been perceived as an important mechanism in some in vivo studies. Accordingly, this study was conducted to identify the potential effects of ZrO2-NPs on rabbit tooth gum cells as well as the mechanism/s of their cytotoxicity. Synthesized ZrO2-NPs were characterized using scanning electron microscopy (SEM), dynamic light scattering (DLS), Cell viability, ROS level, lipid peroxidation (LPO), mitochondrial membrane potential (MMP), glutathione count (GSH/GSSG), lysosome damage and apoptosis/necrosis were evaluated. Biodistribution studies were conducted on tooth gum, liver, kidney, heart and brain tissues in the rabbit using inductively coupled plasma optical emission spectrometry (ICP/OES). ZrO2-NPs increased ROS, MMP collapse and malondialdehyde (MDA). In contrast, GSH/GSSG and apoptosis/necrosis were found to be changed. The ZrO2-NPs accumulated significantly more on rabbit tooth gum tissues compared with other organs ([Formula: see text]). The study provided evidence that ZrO2-NPs cannot be considered completely biocompatible in the gum cell tissues of the rabbit. Before these nanoparticles can be used for human dental applications, further investigations on a wide range of cell death signaling should be performed.

Publisher

World Scientific Pub Co Pte Ltd

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