SIZE DETERMINATION AND MULTIPLEXED FLUORESCENCE-BASED PHENOTYPING OF SINGLE CELL-DERIVED MEMBRANE VESICLES USING A NANOFLUIDIC DEVICE

Lubart, Q.; Levin, S.; de Carvalho, V.; Persson, E.; Block, S.; Joemetsa, S.; Olsen, E.; KK, S.; Gorgens, A.; EL Andaloussi, S.; Hook, F.; Bally, M.; Westerlund, F.; Esbjorner, E. K.

doi:10.64898/2026.04.17.719178

bioRxiv · 10.64898/2026.04.17.719178

SIZE DETERMINATION AND MULTIPLEXED FLUORESCENCE-BASED PHENOTYPING OF SINGLE CELL-DERIVED MEMBRANE VESICLES USING A NANOFLUIDIC DEVICE

Lubart, Q.·Levin, S.·de Carvalho, V.·Persson, E.·Block, S.·Joemetsa, S.·Olsen, E.·KK, S.·Gorgens, A.·EL Andaloussi, S.·Hook, F.·Bally, M.·Westerlund, F.·Esbjorner, E. K.

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Abstract

Extracellular vesicles (EVs) are cell-secreted biological nanoparticles that play a crucial role in intercellular communication and are gaining increasing attention as diagnostic biomarkers, therapeutic agents, and drug delivery vehicles. Consequently, the development of robust and sensitive methods for their characterization is essential. Herein we present the use of a microscope-mounted nanofluidic device for direct size determination and multi-parametric (3-color) fluorescence-based phenotyping of single biological nanoparticles that are in the size range of 20-200 nm in a method we denote Nano-SMF (SMF; size and multiplexed fluorescence). We demonstrate that it is possible to accurately determine the size of nanoparticles by analyzing their one-dimensional Brownian motion during directional flow through nanochannels, achieving size distributions for monodisperse nanoparticle solutions that are on par with TEM analysis, and size discrimination of nanoparticle mixtures that is significantly improved compared to conventional nanoparticle tracking analysis (NTA). Furter, we demonstrate that the method can be applied to analyze EVs directly in minute volumes of cell supernatant, avoiding pre-isolation or concentration steps. The method was applied to phenotype CD63- and CD81-positive EVs from a human embryonic kidney cell model, demonstrating that vesicle sub-populations defined by these two tetraspanin biomarkers differ significantly in size.

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Lubart, Q., Levin, S., de Carvalho, V., Persson, E., Block, S., Joemetsa, S., Olsen, E., KK, S., Gorgens, A., EL Andaloussi, S., Hook, F., Bally, M., Westerlund, F., Esbjorner, E. K.. 2026-04-21. SIZE DETERMINATION AND MULTIPLEXED FLUORESCENCE-BASED PHENOTYPING OF SINGLE CELL-DERIVED MEMBRANE VESICLES USING A NANOFLUIDIC DEVICE. https://doi.org/10.64898/2026.04.17.719178

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