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        Figure 11.5  Transmission electron micrograph of human epidermal keratinocyte
        exposed to QD 655 with a carboxylic acid surface coating at 24 hours. Arrow depicts
        QD within a cytoplasmic vacuole.


        size and surface coating (Figure 11.5). However, the cytotoxic and inflam-
        matory effects of QD were dependent upon their surface coating, with
        a modulatory role for size on cytokine release. Quantum dots and other
        nanostructures are expected to have high inflammatory potential due
        to a large surface area to volume ratio (Oberdorster et al., 2005). Similar
        to the preferential uptake of anionic ferric nanoparticles in cells dis-
        cussed above, our studies showed carboxylated anionic QD accumu-
        lated the most in cells and were most cytotoxic. This study is the first
        account of QD uptake, cytotoxicity, and inflammation in human epi-
        dermal keratinocytes (Ryman-Rasmussen et al., 2007).
          Other studies have shown how QD can act as fluorescence labels for
        biological and biomedical cellular imaging. Wu et al. (2003) synthesized
        specific immunofluorescent probes by linking QD to streptavidin and
        IgGs to label breast cancer marker Her2 on the surface of fixed and live
        cancer cells. They conducted labeling efficiency studies of these probes
        in targets such as cell surface receptors, cytoskeleton components, and
        nuclear image antigens at different cellular locations, including cell
        surface, intracellular, and intranuclear. Multiphoton fluorescence imag-
        ing of water-soluble QD in mice were conducted to compare conven-
        tional fluorescein isothiocyanate conjugated to dextran beads. They
        were found to be superior and achieved greater depths using less power,
        especially in high scattering skin and adipose tissue. Mice showed no
        noticeable ill effects (Larson et al., 2003). Noninvasive imaging of four
        different QD coatings were tested in mice. The QD circulating half-lives
        were less than 12 minutes for amphiphilic poly (acrylic acid), short
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