Complete surgical resection is the first-line treatment for most liver
malignancies. This goal would be facilitated by an intraoperative imaging method
that enables more precise visualization of tumor margins, and detection of
otherwise invisible microscopic lesions. To this end, we synthesized
silica-encapsulated surface-enhanced Raman scattering (SERS) nanoparticles (NPs)
that act as a molecular imaging agent for liver malignancies. We hypothesized
that, after intravenous administration, SERS NPs would avidly home to healthy
liver tissue, but not to intrahepatic malignancies. We tested these SERS NPs in
genetically engineered mouse models of hepatocellular carcinoma and histiocytic
sarcoma. After intravenous injection, liver tumors in both models were readily
identifiable with Raman imaging. In addition, Raman imaging using SERS NPs
enabled detection of microscopic lesions in liver and spleen. We compared the
performance of SERS NPs to fluorescence imaging using Indocyanine Green (ICG).
We found that SERS NPs delineate tumors more accurately and are less susceptible
to photobleaching. Given the known advantages of SERS imaging, namely high
sensitivity and specific spectroscopic detection, these findings hold promise
for improved resection of liver cancer.