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SHINE: SERS-based Hepatotoxicity detection using Inference from Nanoscale Extracellular vesicle content
Ugur Parlatan1, Luke Boudreau2,3, Hulya Torun1
1Bio-Acoustic MEMS in Medicine (BAMM) Lab, Canary Center at Stanford, Department of Radiology, School of Medicine, Stanford University, California, CA, 94304, USA.
Biorxiv : the Preprint Server for Biology
|February 20, 2025
Summary
This study introduces a rapid, label-free surface-enhanced Raman spectroscopy (SERS) method for analyzing extracellular vesicles (EVs). The technique detects molecular changes in EVs, enabling early identification of drug-induced liver injury (hepatotoxicity).
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Spectroscopy
Background:
- Extracellular vesicles (EVs) are vital for diagnostics and therapeutics but challenging to characterize at the nanoscale.
- Detecting drug-induced liver injury (hepatotoxicity) via EV molecular content is an emerging, unexplored area.
Purpose of the Study:
- To develop a rapid, label-free surface-enhanced Raman spectroscopy (SERS) platform for analyzing EV molecular content.
- To investigate the potential of this platform for detecting drug-induced hepatotoxicity using EV signatures.
Main Methods:
- A novel SERS spectroscopy approach was employed for EV analysis.
- The platform requires minimal sample volume (1.3 microliters) and provides results in under ten minutes.
- Hepatic cell cultures were used to model acetaminophen-induced hepatotoxicity.
Main Results:
- The platform successfully captured distinct and reproducible EV molecular changes in response to hepatotoxicity.
- High accuracy was achieved, with root mean squared error as low as 3.80%.
- Strong correlations were established between EV spectral data and conventional toxicity biomarkers, revealing drug-response signatures.
Conclusions:
- Extracellular vesicles serve as dynamic reporters of cellular drug responses.
- SERS-based EV detection offers a promising method for identifying and monitoring drug-induced hepatotoxicity.

