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Identification of the mechanisms that drive the toxicity of TiO2 particulates: the contribution of physicochemical characteristics

Helinor J Johnston1,2 email, Gary R Hutchison1 email, Frans M Christensen3 email, Sheona Peters4 email, Steve Hankin4 email and Vicki Stone1 email

Centre for Nano Safety, School of Life Sciences, Edinburgh Napier University, Edinburgh EH10 5DT, UK

Department for Environment, Food and Rural Affairs, Chemicals and Nanotechnologies Division, Area 2a Nobel House, 17 Smith Square, London SW1P 3JR, UK

Nanobiosciences unit, European Commission - DG Joint Research Centre (JRC), Institute for Health and Consumer Protection (IHCP), Via E. Fermi, 2749, I - 21027 Ispra, Italy

Institute of Occupational Medicine, Research Avenue North, Riccarton, Edinburgh, EH14 4AP, UK

author email corresponding author email

Particle and Fibre Toxicology 2009, 6:33doi:10.1186/1743-8977-6-33

Published: 17 December 2009

Abstract

This review focuses on outlining the toxicity of titanium dioxide (TiO2) particulates in vitro and in vivo, in order to understand their ability to detrimentally impact on human health. Evaluating the hazards associated with TiO2 particles is vital as it enables risk assessments to be conducted, by combining this information with knowledge on the likely exposure levels of humans. This review has concentrated on the toxicity of TiO2, due to the fact that the greatest number of studies by far have evaluated the toxicity of TiO2, in comparison to other metal oxide particulates. This derives from historical reasons (whereby the size dependency of particulate toxicity was first realised for TiO2) and due to its widespread application within consumer products (such as sunscreens). The pulmonary and dermal hazards of TiO2 have been a particular focus of the available studies, due to the past use of TiO2 as a (negative) control when assessing the pulmonary toxicity of particulates, and due to its incorporation within consumer products such as sunscreens. Mechanistic processes that are critical to TiO2 particulate toxicity will also be discussed and it is apparent that, in the main, the oxidant driven inflammatory, genotoxic and cytotoxic consequences associated with TiO2 exposure, are inherently linked, and are evident both in vivo and in vitro. The attributes of TiO2 that have been identified as being most likely to drive the observed toxicity include particle size (and therefore surface area), crystallinity (and photocatalytic activity), surface chemistry, and particle aggregation/agglomeration tendency. The experimental set up also influences toxicological outcomes, so that the species (or model) used, route of exposure, experiment duration, particle concentration and light conditions are all able to influence the findings of investigations. In addition, the applicability of the observed findings for particular TiO2 forms, to TiO2 particulates in general, requires consideration. At this time it is inappropriate to consider the findings for one TiO2 form as being representative for TiO2 particulates as a whole, due to the vast number of available TiO2 particulate forms and large variety of potential tissue and cell targets that may be affected by exposure. Thus emphasising that the physicochemical characteristics are fundamental to their toxicity.


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