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193689 
Journal Article 
Comparing fate and effects of three particles of different surface properties: Nano-TiO2, pigmentary TiO2 and quartz 
Van Ravenzwaay, B; Landsiedel, R; Fabian, E; Burkhardt, S; Strauss, V; Ma-Hock, L 
2009 
1 
Toxicology Letters
ISSN: 0378-4274
EISSN: 1879-3169 
186 
3 
152-159 
English 
19114093 
WOS:000265136200003 
The fate of nano-TiO2 particles in the body was investigated after inhalation exposure or intravenous (i.v.) injection, and compared with pigmentary TiO2 and quartz. For this purpose, a 5-day inhalation study (6 h/day, head/nose exposure) was carried out in male Wistar rats using nano-TiO2 (100 mg/m3), pigmentary TiO2 (250 mg/m3) and quartz dust DQ 12 (100 mg/m3). Deposition in the lung and tissue distribution was evaluated, and histological examination of the respiratory tract was performed upon termination of exposure, and 2 weeks after the last exposure. Broncho-alveolar lavage (BAL) was carried out 3 and 14 days after the last exposure. Rats were also injected with a single intravenous dose of a suspension of TiO2 in serum (5 mg/kg body weight), and tissue content of TiO2 was determined 1, 14 and 28 days later. The majority of the inhaled nano-TiO2 was deposited in the lung. Translocation to the mediastinal lymph nodes was also noted, although to smaller amounts than following inhalation of pigmentary TiO2, but much higher amounts than after exposure to quartz. Systemically available nano-TiO2, as simulated by the i.v. injection, was trapped mainly in the liver and spleen. The (agglomerate) particle size of lung deposited nano-TiO2 was virtually the same as in the test atmosphere. Changes in BAL fluid composition and histological examination indicated mild neutrophilic inflammation and activation of macrophages in the lung. The effects were reversible for nano- and pigmentary TiO2, but progressive for quartz. The effects observed after 5-day inhalation exposure to nano-TiO2 were qualitatively similar to those reported in sub-chronic studies. 
Nano-TiO2; Quartz DQ 12; Surface area; Surface reactivity; Distribution; Toxic effects