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.

Highlights

  • The field of nanotechnology is expanding at a tremendous rate due to the realisation that the properties exhibited by materials at a 'nano' scale are often exceedingly different to those demonstrated by bulk forms of the same material

  • Inflammation (BALF analysis) Epithelial cell damage Lung permeability (BALF protein) Cytotoxicity (BALF lactate dehydrogenase (LDH)) Macrophage phagocytic ability Macrophage chemotaxis

  • NPs stimulate pulmonary inflammation, epithelial damage and cytotoxicity to a greater extent than their fine counterparts The phagocytic ability of macrophages was impaired with NP exposure but not fine particles

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Summary

Introduction

The field of nanotechnology is expanding at a tremendous rate due to the realisation that the properties exhibited by materials at a 'nano' scale are often exceedingly different to those demonstrated by bulk forms of the same material. An improved understanding of the potential risks (comprising of exposure and hazard assessments) of such materials is required, and in particular, determination of nanomaterial characteristics that may detrimentally affect human health (see for example, Maynard et al [2]) This knowledge will be useful in managing risk in the future, by allowing the implementation of specific control measures for minimising exposure to such materials, perhaps through the introduction of regulations, or through the use of alternative materials. TiO2 has been largely used in pulmonary toxicology studies as a negative control when assessing the toxicity of pathogenic particulates such as alpha-quartz As a result, this had to be re-considered based on the apparent size dependency of TiO2 toxicity. Rats were administered TiO2 of various sizes (12, 21, 230 and 250 nm in diameter) via a single intrat-

Findings
Conclusion
Findings Pulmonary inflammation greatest for NPs
Conclusions
BSi Report
73. Oberdorster G
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