Hepatotoxicity of titanium dioxide nanoparticles.

IF 2.7 4区 医学 Q3 TOXICOLOGY
Jangrez Khan, Nicholas D Kim, Collette Bromhead, Penelope Truman, Marlena C Kruger, Beth L Mallard
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引用次数: 0

Abstract

The food additive E171 (titanium dioxide, TiO2), is widely used in foods, pharmaceuticals and cosmetics. It is a fine white powder, with at least one third of its particles sized in the nanoparticulate (˂100 nm range, TiO2 NPs). The use of E171 is controversial as its relevant risk assessment has never been satisfactorily accomplished. In vitro and in vivo studies have shown dose-dependent toxicity in various organs including the liver. TiO2 NPs have been shown to induce inflammation, cell death and structural and functional changes within the liver. The toxicity of TiO2 NPs in experimental models varies between organs and according to their physiochemical characteristics and parameters such as dosage and route of administration. Among these factors, ingestion is the most significant exposure route, and the liver is a key target organ. The aim of this review is to highlight the reported adverse effects of orally administered TiO2 NPs on the liver and to discuss the controversial state of its toxicity.

纳米二氧化钛的肝毒性。
食品添加剂 E171(二氧化钛,TiO2)广泛用于食品、药品和化妆品。它是一种精细的白色粉末,至少有三分之一的颗粒大小为纳米颗粒(˂100 纳米范围,TiO2 NPs)。E171 的使用存在争议,因为其相关风险评估从未令人满意地完成。体外和体内研究表明,E171 对包括肝脏在内的各种器官具有剂量依赖性毒性。研究表明,二氧化钛纳米粒子可诱发肝脏炎症、细胞死亡以及结构和功能变化。二氧化钛纳米粒子在实验模型中的毒性因器官而异,也因其理化特性和参数(如剂量和给药途径)而异。在这些因素中,摄入是最主要的暴露途径,而肝脏是关键的靶器官。本综述旨在强调已报道的口服 TiO2 NPs 对肝脏的不良影响,并讨论其毒性的争议状况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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