US EPA

91106 

Journal Article 

Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature 

Muhlfeld, C; Geiser, M; Kapp, N; Gehr, P; Rothen-Rutishauser, B 

2007 

1 

Particle and Fibre Toxicology
EISSN: 1743-8977 

4 

7 

Background
Translocation of nanoparticles (NP) from the pulmonary airways into other pulmonary compartments or the systemic circulation is controversially discussed in the literature. In a previous study it was shown that titanium dioxide (TiO2) NP were "distributed in four lung compartments (air-filled spaces, epithelium/endothelium, connective tissue, capillary lumen) in correlation with compartment size". It was concluded that particles can move freely between these tissue compartments. To analyze whether the distribution of TiO2 NP in the lungs is really random or shows a preferential targeting we applied a newly developed method for comparing NP distributions.
Methods
Rat lungs exposed to an aerosol containing TiO2 NP were prepared for light and electron microscopy at 1h and at 24h after exposure. Numbers of TiO2 NP associated with each compartment were counted using energy filtering transmission electron microscopy. Compartment size was estimated by unbiased stereology from systematically sampled light micrographs. Numbers of particles were related to compartment size using a relative deposition index and chi-squared analysis.
Results
Nanoparticle distribution within the four compartments was not random at 1h or at 24h after exposure. At 1h the connective tissue was the preferential target of the particles. At 24h the NP were preferentially located in the capillary lumen.
Conclusions
We conclude that TiO2 NP do not move freely between pulmonary tissue compartments, although they can pass from one compartment to another with relative ease. The residence time of NP in each tissue compartment of the respiratory system depends on the compartment and the time after exposure. It is suggested that a small fraction of TiO2 NP are rapidly transported from the airway lumen to the connective tissue and subsequently released into the systemic circulation.