Patients with nonimmediate reactions to CM were identified by skin testing in 43.6% and by DPT in 56.4%. The method to confirm the diagnosis differed depending on the CM involved.
Understanding
how ultrasmall gold nanoparticles (metal core ∼1–1.5
nm), so-called gold nanoclusters (Au NCs), interact with biological
barriers has become highly important for their future bioapplications.
The properties of Au NCs with tunable hydrophobicity were extensively
characterized in three different biological situations: (i) interaction
with serum in solution, (ii) interaction with synthetic free-standing
lipid bilayers integrated in a microfluidic device, and (iii) cell
studies with two different cell types (U87MG human primary glioblastoma
and A375 melanoma cell lines). Our results indicate a significant
impact of the precise tailoring of the hydrophilicity/hydrophobicity
balance on the Au NC surfaces, which could prevent the formation of
biomolecular absorption while maintaining excellent colloidal stability
in solutions with high serum contents. Increasing the surface hydrophobicity
of the Au NCs enabled more efficient lipid bilayer membrane insertion
and induced faster cellular uptake. We showed the existence of a hydrophobicity
threshold, which resulted in colloidal instability, lipid bilayer
damage, and acute cytotoxicity. We also demonstrated a significant
influence of metal–ligand shell hydrophobicity on the fluorescence
signal of the Au NCs, increasing it in the near-infrared region. A
twofold signal enhancement was achieved by simple replacement of methyl
groups with ethyl groups.
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