Extracellular vesicles (EVs) are cell-derived membrane-bound
particles
with molecular cargo reflective of their cell of origin. Analysis
of disease-related EVs and associated cargo from biofluids is a promising
tool for disease management. To facilitate the analysis of intravesicular
molecules, EV lysis is needed. Moreover, highly sensitive and multiplexed
detection methods are required to achieve early diagnostics. While
cell lysis approaches have been well studied, the analysis of EV lysis
methods and their effects on downstream molecular detection is lacking.
In this work, we analyzed chemical, thermal, and mechanical EV lysis
methods and determined their efficiency based on EV particle concentration
and immunoassay activity. We, for the first time, discovered that
vortex was an efficient EV lysis method and used it for detection
of surface and intravesicular markers in a highly sensitive multiplexed
reverse phase immunoassay on a gold-nanoparticle-embedded membrane.
In phosphate-buffered saline, detection limits up to 3 orders of magnitude
lower than enzyme-linked immunosorbent assay were achieved. In spiked
human plasma, detection limits as low as 7.27 × 104 EVs/mL were achieved, making it suitable for early diagnostics.
These results demonstrated an effective pipeline for lysing and molecular
analysis of EVs from complex biofluids, paving the way for their broad
applications in biomedicine.