Science and Society (Pelican) by Hilary Rose
By Hilary Rose
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1998); this raises a question about potential modulation of immune responses, after interaction of these NP-containing macrophages and dendritic cells with T lymphocytes. For example, Chen et al. (1998) were able to raise antibodies in mice specific for C60 after intraperitoneal injections of C60 conjugated to thyroglobulin and serum albumin. Clearly, research is needed to determine whether and under what conditions NPs can be recognized by the immune 40 NANOPARTICLE EFFECTS system, following any route of uptake into the organism.
Potential mechanisms of ultrafine particle effects. Once NSPs have translocated to the blood circulation, they can be distributed throughout the body. The liver is the major distribution site via uptake by Kupffer cells, followed by the spleen as another organ of the reticuloendothelial system, although coating with polyethylene glycol (PEG) almost completely prevents hepatic and splenic localization so that other organs can be targeted (Akerman et al. 2002). Distribution to heart, kidney, and immune-modulating organs (spleen, bone marrow) has been reported.
Clearly, research is needed to determine whether and under what conditions NPs can be recognized by the immune 40 NANOPARTICLE EFFECTS system, following any route of uptake into the organism. Another question relates to the potential of sensory skin nerves to take up and translocate NPs. Given that this mechanism has been demonstrated for the nasal and tracheobronchial regions of the respiratory tract, how likely is this to occur in the dermis layer of the skin with its dense supply of different types of considering data on neuronal uptake and translocation of NPs after intramuscular injection.