Titanium Dioxide: Inhalation Toxicology and Epidemiology
| Autor: | Peter Thompson, John A. Tomenson, Paul M. Hext |
|---|---|
| Rok vydání: | 2005 |
| Předmět: |
Lung Diseases
Male Pathology medicine.medical_specialty Hamster Physiology Inhalation Toxicology Mice Species Specificity Cricetinae Animals Humans Medicine Lung cancer Carcinogen Titanium Inhalation Exposure Lung Dose-Response Relationship Drug Inhalation business.industry technology industry and agriculture Public Health Environmental and Occupational Health General Medicine medicine.disease Rats Inbred F344 Rats Europe Occupational Diseases Dose–response relationship medicine.anatomical_structure Toxicity Female business |
| Zdroj: | The Annals of Occupational Hygiene. |
| ISSN: | 1475-3162 |
| DOI: | 10.1093/annhyg/mei012 |
| Popis: | Titanium dioxide (TiO(2)) is manufactured worldwide in large quantities for use in a wide range of applications and is normally considered to be toxicologically inert. Findings of tumours in the lungs of rats exposed chronically to high concentrations of TiO(2), but not in similarly exposed mice or hamsters, suggest that the tumorigenic response may be a rat-specific phenomenon but nonetheless raises concerns for potential human health effects. With the limited toxicological understanding of species differences in response to inhaled TiO(2) and a similarly limited amount of epidemiological information with respect to TiO(2) exposure in the workplace, a consortium of TiO(2) manufacturers in Europe (under the European Chemistry Industry Council; CEFIC) and in North America (under the American Chemistry Council; ACC) initiated a programme of research to investigate inter-species differences as a result of exposure to TiO(2) and to conduct detailed epidemiological surveys of the major manufacturing sites. The toxicology studies exposed rats, mice and hamsters to pigment-grade TiO(2) (PG-TiO(2), 0, 10, 50 and 250 mg m(-3)) or ultrafine TiO(2) (UF-TiO(2), 0, 0.5, 2 and 10 mg m(-3)) for 90 days and the lung burdens and tissue responses were evaluated at the end of the exposure period and for up to 1 year after exposure. Results demonstrated clear species differences. Rats and mice had similar lung burdens and clearance rates while hamsters showed high clearance rates. At high lung particle burdens, rats showed a marked progression of histopathological lesions throughout the post-exposure period while mice and hamsters showed minimal initial lesions with recovery apparent during the post-exposure period. Lung neutrophil responses, a sensitive marker of inflammatory changes, reflected the development or recovery of the histopathological lesions. The use of surface area rather than gravimetric lung burden provided closer correlates of the burden to the biological effect across both TiO(2) types. The epidemiological investigations evaluated the mortality statistics at 11 European and 4 US TiO(2) manufacturing plants. They concluded that there was no suggestion of any carcinogenic effect associated with workplace exposure to TiO(2). |
| Databáze: | OpenAIRE |
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