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.

Highlights

  • Recent advances of nanotechnology in materials science have led to the development of novel materials of various types at the nanoscale level

  • Oxidative stress and endoplasmic reticulum (ER) stress involve in liver injury, triggering caspase 3, caspase 9 and caspase 12, and up-regulation of C/EBP homologous protein (CHOP) and bax expressions Elevated alanine transaminase (ALT) and alkaline phosphatase (ALP) levels in serum, and accumulation of zinc oxide (ZnO) NPs in liver at a high dose of 300 mg/kg, causing reactive oxygen species (ROS) production and deoxyribonucleic acid (DNA) damage in liver

  • The FDA approves ZnO as a GRAS material having extensive applications in cosmetics, food additives, and healthcare products. This approval is mainly designated for ZnO microparticles

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Summary

Introduction

Recent advances of nanotechnology in materials science have led to the development of novel materials of various types at the nanoscale level. Typical examples are carbon quantum dots (0-D), carbon or titania nanotubes (1-D), graphene sheets (2-D), and zinc oxide nanoflowers (3-D). Those functional materials can be fabricated at nanometer-scale control and precision. PDT treatment involves the generation of ROS from a photosensitizer injected into human body under a suitable excitation light source [37]. Semiconductor oxide nanoparticles such as ZnO NPs and TiO2 NPs capable of generating ROS under UV light for cancer treatment is attractive for the PDT [38,39]. The nZnO-induced toxicity mediated by ROS generation under UV irradiation for human cancer cell therapy is addressed

Structure-Dependent Photocatalytic Activity
Sol-Gel Technique
Photocatalytic Toxicity
Findings
Conclusions and Outlook
Full Text
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