Fluorescence-based expansion microscopy (ExM) is a new technique which can yield nanoscale resolution of biological specimen on a conventional fluorescence microscope through physical sample expansion up to 20 times its original dimensions while preserving structural information. It however inherits known issues of fluorescence microscopy such as photostability and multiplexing capabilities, as well as an ExM-specific issue in signal intensity reduction due to a dilution effect after expansion. To address these issues, we propose using antigen-targeting plasmonic nanoparticle labels which can be imaged using surface-enhanced Raman scattering spectroscopy (SERS) and dark-field spectroscopy. We demonstrate that the nanoparticles enable multimodal imaging: bright-field, dark-field and SERS, with excellent photostability, contrast enhancement and brightness.
Keywords: (170.3880) Medical and biological imaging; (170.5660) Raman spectroscopy; (170.6510) Spectroscopy, tissue diagnostics; (170.6935) Tissue characterization; (180.5655) Raman microscopy; (240.6680) Surface plasmons; (240.6695) Surface-enhanced Raman scattering.