# Rapid trapping and label-free optical characterization of single nanoscale extracellular vesicles and nanoparticles in solution

**Authors:** Ikjun Hong, Chuchuan Hong, Theodore Anyika, Guodong Zhu, Maxwell Ugwu, James N. Higginbotham, Jeffrey L. Franklin, Robert Coffey, Justus C. Ndukaife

PMC · DOI: 10.1038/s41377-026-02201-z · 2026-03-20

## TL;DR

A new platform called IET rapidly traps and analyzes nanoscale particles in solution, enabling fast and detailed characterization of their size and chemical makeup.

## Contribution

IET combines trapping, interferometric imaging, and Raman spectroscopy in one system for rapid, label-free analysis of nanoparticles and extracellular vesicles.

## Key findings

- IET can trap and characterize nanoparticles within seconds, much faster than traditional laser trapping methods.
- The platform works effectively even at low particle concentrations, where conventional methods struggle.
- IET successfully analyzed the size and chemical composition of both polymer beads and extracellular vesicles in solution.

## Abstract

Achieving high-efficiency, comprehensive analysis of single nanoparticles to determine their size, shape, and composition is essential for understanding particle heterogeneity with applications ranging from drug delivery to environmental monitoring. Existing techniques are hindered by low throughput, lengthy trapping times, irreversible particle adsorption, or limited characterization capabilities. Here, we introduce Interferometric Electrohydrodynamic Tweezers (IET), an integrated platform that combines rapid molecular trapping, interferometric scattering imaging, and Raman scattering to rapidly trap and characterize single nanoparticles within seconds in one integrated platform. The IET platform enables to perform both trapping and Raman analysis within seconds in contrast with laser trapping Raman spectroscopy that often require several minutes per measurement. Furthermore, the IET platform can also operate under low particle concentration media, where particle loading is slow for conventional laser trapping Raman spectroscopy approach. We demonstrate the platform’s capabilities by trapping and characterizing the size and chemical composition of colloidal polymer beads and nanoscale extracellular vesicles (EVs), while trapped in solution. Our IET represents a powerful optofluidics platform for comprehensive characterization of nanoscale objects, opening new avenues in nanomedicine, environmental monitoring, and beyond.

Interferometric Electrohydrodynamic Tweezers (IET) uniquely integrates parallel trapping with label-free interferometric imaging and non-destructive Raman spectroscopy for simultaneous sizing and chemical characterization of nanoscale extracellular vesicles and nanoparticles.

## Full-text entities

- **Genes:** TMC6 (transmembrane channel like 6) [NCBI Gene 11322] {aka EV1, EVER1, EVIN1, LAK-4P, TNRC6C-AS1, lnc}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, TMC8 (transmembrane channel like 8) [NCBI Gene 147138] {aka EV2, EVER2, EVIN2}
- **Chemicals:** purine (MESH:C030985), Cr (MESH:D002857), 1x PBS (-), acetone (MESH:D000096), PS (MESH:D011137), amide (MESH:D000577), Au (MESH:D006046), lipid (MESH:D008055), PBS (MESH:D007854), water (MESH:D014867), SiO2 (MESH:D012822)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13002945/full.md

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Source: https://tomesphere.com/paper/PMC13002945