Noble metal nanoparticles (NPs) supporting localized surface plasmon resonances are widely
used in the context of biotechnology as optical and absorption contrast agents with great potential
applicability to both diagnostics and less invasive therapies. In this framework, it is crucial to have
access to simple and reliable microscopy techniques to monitor the NPs that have internalized
into cells. While dark field (DF) microscopy takes advantage of the enhanced NPs scattering at
their plasmon resonance, its use in cells is limited by the large scattering background from the
internal cell compartments. Here, we report on a novel two-color dark field microscopy that addresses
these limitations by significantly reducing the cell scattering contribution. We first present
the technique and demonstrate its enhanced contrast, specificity and reliability for NP detection
compared to standard optical dark field. We then demonstrate its potential suitability in two different
settings, namely wide-field parallel screening of circulating cells in microfluidic chip and
high-resolution tracking of internalized NPs in cells. These proof of principle experiments show a
promising capability of this approach with possible extension to other kinds of targeted systems
like bacteria and vesicles.Peer Reviewe