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Review

Interactions of Zinc Oxide Nanostructures with Mammalian Cells: Cytotoxicity and Photocatalytic Toxicity

1
Department of Materials Science and Engineering, Southern University of Science and Technology, Shenzhen 518055, China
2
Department of Materials Science and Engineering, Liaocheng University, Liaocheng 252000, China
3
Department of Physics, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, China
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2020, 21(17), 6305; https://doi.org/10.3390/ijms21176305
Submission received: 20 August 2020 / Accepted: 28 August 2020 / Published: 31 August 2020
(This article belongs to the Special Issue Cell-Biomaterial Interaction 2020)

Abstract

This article presents a state-of-the-art review and analysis of literature studies on the morphological structure, fabrication, cytotoxicity, and photocatalytic toxicity of zinc oxide nanostructures (nZnO) of mammalian cells. nZnO with different morphologies, e.g., quantum dots, nanoparticles, nanorods, and nanotetrapods are toxic to a wide variety of mammalian cell lines due to in vitro cell–material interactions. Several mechanisms responsible for in vitro cytotoxicity have been proposed. These include the penetration of nZnO into the cytoplasm, generating reactive oxygen species (ROS) that degrade mitochondrial function, induce endoplasmic reticulum stress, and damage deoxyribonucleic acid (DNA), lipid, and protein molecules. Otherwise, nZnO dissolve extracellularly into zinc ions and the subsequent diffusion of ions into the cytoplasm can create ROS. Furthermore, internalization of nZnO and localization in acidic lysosomes result in their dissolution into zinc ions, producing ROS too in cytoplasm. These ROS-mediated responses induce caspase-dependent apoptosis via the activation of B-cell lymphoma 2 (Bcl2), Bcl2-associated X protein (Bax), CCAAT/enhancer-binding protein homologous protein (chop), and phosphoprotein p53 gene expressions. In vivo studies on a mouse model reveal the adverse impacts of nZnO on internal organs through different administration routes. The administration of ZnO nanoparticles into mice via intraperitoneal instillation and intravenous injection facilitates their accumulation in target organs, such as the liver, spleen, and lung. ZnO is a semiconductor with a large bandgap showing photocatalytic behavior under ultraviolet (UV) light irradiation. As such, photogenerated electron–hole pairs react with adsorbed oxygen and water molecules to produce ROS. So, the ROS-mediated selective killing for human tumor cells is beneficial for cancer treatment in photodynamic therapy. The photoinduced effects of noble metal doped nZnO for creating ROS under UV and visible light for killing cancer cells are also addressed.
Keywords: Zinc Oxide; metal doping; plasmonic nanoparticle; oxidative stress; zincate; photodynamic therapy; ultraviolet light; cancer cell; mouse model Zinc Oxide; metal doping; plasmonic nanoparticle; oxidative stress; zincate; photodynamic therapy; ultraviolet light; cancer cell; mouse model
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MDPI and ACS Style

Liao, C.; Jin, Y.; Li, Y.; Tjong, S.C. Interactions of Zinc Oxide Nanostructures with Mammalian Cells: Cytotoxicity and Photocatalytic Toxicity. Int. J. Mol. Sci. 2020, 21, 6305. https://doi.org/10.3390/ijms21176305

AMA Style

Liao C, Jin Y, Li Y, Tjong SC. Interactions of Zinc Oxide Nanostructures with Mammalian Cells: Cytotoxicity and Photocatalytic Toxicity. International Journal of Molecular Sciences. 2020; 21(17):6305. https://doi.org/10.3390/ijms21176305

Chicago/Turabian Style

Liao, Chengzhu, Yuming Jin, Yuchao Li, and Sie Chin Tjong. 2020. "Interactions of Zinc Oxide Nanostructures with Mammalian Cells: Cytotoxicity and Photocatalytic Toxicity" International Journal of Molecular Sciences 21, no. 17: 6305. https://doi.org/10.3390/ijms21176305

APA Style

Liao, C., Jin, Y., Li, Y., & Tjong, S. C. (2020). Interactions of Zinc Oxide Nanostructures with Mammalian Cells: Cytotoxicity and Photocatalytic Toxicity. International Journal of Molecular Sciences, 21(17), 6305. https://doi.org/10.3390/ijms21176305

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