Interactions of Zinc Oxide Nanostructures with Mammalian Cells : Cytotoxicity and Photocatalytic Toxicity
Research output: Journal Publications and Reviews › RGC 62 - Review of books or of software (or similar publications/items) › peer-review
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Detail(s)
Original language | English |
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Article number | 6305 |
Number of pages | 49 |
Journal / Publication | International Journal of Molecular Sciences |
Volume | 21 |
Issue number | 17 |
Online published | 31 Aug 2020 |
Publication status | Published - Sept 2020 |
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DOI | DOI |
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Link to Scopus | https://www.scopus.com/record/display.uri?eid=2-s2.0-85090241528&origin=recordpage |
Permanent Link | https://scholars.cityu.edu.hk/en/publications/publication(b5ace11e-b034-4afe-a579-354c6f0eb285).html |
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.
Research Area(s)
- Cancer cell, Metal doping, Mouse model, Oxidative stress, Photodynamic therapy, Plasmonic nanoparticle, Ultraviolet light, Zinc Oxide, Zincate
Citation Format(s)
Interactions of Zinc Oxide Nanostructures with Mammalian Cells: Cytotoxicity and Photocatalytic Toxicity. / Liao, Chengzhu; Jin, Yuming; Li, Yuchao et al.
In: International Journal of Molecular Sciences, Vol. 21, No. 17, 6305, 09.2020.
In: International Journal of Molecular Sciences, Vol. 21, No. 17, 6305, 09.2020.
Research output: Journal Publications and Reviews › RGC 62 - Review of books or of software (or similar publications/items) › peer-review
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