posted on 2020-09-16, 12:34authored byTatu Rojalin, Hanna J. Koster, Juanjuan Liu, Rachel R. Mizenko, Di Tran, Sebastian Wachsmann-Hogiu, Randy P. Carney
For
more effective early-stage cancer diagnostics, there is a need
to develop sensitive and specific, non- or minimally invasive, and
cost-effective methods for identifying circulating nanoscale extracellular
vesicles (EVs). Here, we report the utilization of a simple plasmonic
scaffold composed of a microscale biosilicate substrate embedded with
silver nanoparticles for surface-enhanced Raman scattering (SERS)
analysis of ovarian and endometrial cancer EVs. These substrates are
rapidly and inexpensively produced without any complex equipment or
lithography. We extensively characterize the substrates with electron
microscopy and outline a reproducible methodology for their use in
analyzing EVs from in vitro and in vivo biofluids. We report effective
chemical treatments for (i) decoration of metal surfaces with cysteamine
to nonspecifically pull down EVs to SERS hotspots and (ii) enzymatic
cleavage of extraluminal moieties at the surface of EVs that prevent
localization of complementary chemical features (lipids/proteins)
to the vicinity of the metal-enhanced fields. We observe a major loss
of sensitivity for ovarian and endometrial cancer following enzymatic
cleavage of EVs’ extraluminal domain, suggesting its critical
significance for diagnostic platforms. We demonstrate that the SERS
technique represents an ideal tool to assess and measure the high
heterogeneity of EVs isolated from clinical samples in an inexpensive,
rapid, and label-free assay.