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Updated: Apr 12, 2026
Using Nanoplasmon-Enhanced Scattering and Low-Magnification Microscope Imaging to Quantify Tumor-Derived Exosomes
Published on: May 24, 2019
Digital Profiling Subpopulations of Cancer Cell-Derived Exosomes via Aptamer-SERS Nanotags on a Wafer-Level
Chunyan Zhu1, Xiaodong Lin2, Ruyun Jin1
1The Key Laboratory of Cognitive Science of State Ethnic Affairs Commission, Hubei Key Laboratory of Medical Information Analysis and Tumor Diagnosis and Treatment, College of Biomedical Engineering, South-Central Minzu University, Wuhan 430074, China.
Abstract:
The clinical translation of exosome-based diagnostics and therapies is hindered by significant molecular heterogeneity. Current exosome phenotyping methods suffer from insufficient sensitivity, limited multiplexing capability, and poor scalability. To address these challenges, we developed a digital wafer-level micropillar array (WLM-Exo) platform. The chip features a high-surface-area micropillar array functionalized with a DSPE-PEG2000 lipid layer via Au-S bonding, enabling lipid-mediated membrane fusion for universal exosome enrichment and a uniform spatial distribution. Following capture, aptamer-based SERS nanotags bind specifically to target proteins on exosomes, generating distinct Raman signals upon laser excitation. Exosomal proteins are digitally quantified by measuring the activated area in the Raman images, exhibiting a log-log linear correlation with exosome concentration. The WLM-Exo platform demonstrates ultrasensitive detection (LOD: 2.11 particles/μL for CD63, 1.17 particles/μL for EpCAM, and 18.3 particles/μL for dual-biomarkers) and simultaneous tetra-color exosomal phenotyping capability. By enabling precise, scalable, and digital protein profiling, this technology offers significant potential for exosomes subtyping in personalized cancer diagnostics and therapeutics monitoring.
