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420   Potential Impacts of Nanomaterials

        substantial effect on free radical generation (Chignell and Sik, 1998;
        Scaiano, 1997). Experimental results have demonstrated that iron-oxygen
        complexes may be a more effective catalyst for free radical damage in
        brain tissue than the Fenton reaction (Schafer et al., 2000). These effects
        are achieved through strong, local magnetic fields generated by biogenic
        magnetite particles that stabilize triplet states during biochemical reac-
        tions taking place nearby (Dobson, 2001). This leads to the production of
        membrane-damaging free radicals and changes in reaction yields. Even
        relatively weak magnetic fields can have a strong influence on reaction
        yields (Brocklehurst et al., 1996). In addition, Fe (II) in magnetite can be
        readily oxidized (forming maghemite) and this process, together with
        local magnetic field effects, may influence L-amyloid production and
        aggregation (Dobson, 2001). This is particularly relevant considering
        studies have shown that iron promotes aggregation of L-amyloid pep-
        tides in vitro and that L-amyloid potentiates free radical formation by sta-
        bilizing ferrous iron (Dobson, 2001; Mantyh et al., 1993; Yang et al., 1999).
          Based on the involvement of iron in the pathogenesis of important
        neurodegenerative diseases in humans, the neurological toxicity of iron
        nanoparticles should be carefully addressed, using long-term animal
        exposure, for each type of iron oxide nanoparticles, including those dif-
        fering in terms of coating.


        Cerium Dioxides

        Cerium oxide has been widely investigated because of its multiple
        applications—as a catalyst, an electrolyte material of solid oxide fuel
        cells, a material of high refractive index, and an insulating layer on
        silicon substrates. The transport and uptake of industrially important
        cerium oxide nanoparticles into human lung fibroblasts has been meas-
        ured in vitro after exposing thoroughly characterized particle suspen-
        sions to fibroblasts with four separate size fractions and concentrations
        ranging from 100 ng/g to 100 µg/g of fluid (100 ppb to 100 ppm). At
        physiologically relevant concentrations, a strong dependence of the
        amount of incorporated ceria on particle size was reported, while
        nanoparticle number density or total particle surface area was of minor
        importance (Ludwig et al.). In fact, the rapid formation of agglomerates
        in the liquid was strongly favored for small particles due to a high
        number density, while larger ones are mainly unagglomerated (Ludwig
        et al., 2005). In fact, the biological uptake process on the surface of the
        cell was faster than the physical transport to the cell. By comparing the
        colloid stability of a series of oxide nanoparticles, one can hypothesize
        that untreated oxide suspensions rapidly agglomerate in biological
        fluids. Thus, the transport and uptake kinetics at low concentrations
        may be extended to other industrially relevant materials.
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