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Nano Letters: Optoseeker Breaks Protein Detection Limits—15 Min Label-Free Hepatitis Test

2025-03-21

A multidisciplinary team from Beijing Institute of Technology, University of Toronto, and other institutions has published groundbreaking research titled "Automated Electroosmotic Digital Optofluidics for Rapid and Label-Free Protein Detection" in Nano Letters.

Automated Electroosmotic Digital Optofluidics for Rapid and Label-Free Protein Detection

As a key technical partner, ​​Optoseeker​​ contributed to digital microfluidic chip design and validation protocols, supported fluorescence tracing experiments using its ​​DropletBot®Digital Microfluidics Platform​​, and was acknowledged in the paper.

The team developed an electroosmotic digital optofluidics (e-DOF) platform that quantifies protein-binding-induced nanoscale deformations via hyperspectral interferometric computation. By integrating electroosmosis-driven molecular self-circulation technology, the detection time was slashed from 2–3 hours (traditional ELISA) to ​​15 minutes​​, achieving a sensitivity of ​​0.21 nM​​ (>50× more sensitive than ELISA) and ​​100% accuracy in clinical samples​​.

I. Journal Profile

Nano Letters (American Chemical Society) is a top-tier journal renowned for pioneering high-impact research at the intersection of nanotechnology and biomedicine. Key metrics:

  • ​Impact Factor (2024): 9.6​
  • ​JCR Quartile: Q1​
  • CAS Rating: Materials Science, Tier 1

II. Research Highlights

1. Label-Free Ultrasensitive Detection


Characterization, optimization, and validation data

  • ​Innovation​​: First e-DOF platform combining hyperspectral interferometry to directly quantify protein-binding nanoscale deformations.
  • ​Performance​​: Detection limit of ​​0.21 nM​​ (50× more sensitive than ELISA), no enzymatic labeling required.

2. Electroosmotic Molecular Flow Acceleration

  • ​Technology​​: Electroosmosis-driven self-circulation accelerates probe-protein binding in 4 μL samples.
  • ​Result​​: Detection completed in ​​15 minutes​​ (vs. ELISA’s 2–3 hrs) with 100% clinical accuracy.
    (Fig. 3: Microfluidic droplet circulation dynamics)
Microfluidic droplet circulation dynamics

3. Fully Automated Integrated Platform

  • ​Design​​: Combines digital microfluidic chips with optical supercomputing modules.
  • ​Workflow​​: Fully automated sample separation-reaction-wash-detection; supports multiplex detection (e.g., HAV/HEV IgM) for point-of-care testing (POCT).
    (Fig. 4: On-chip detection performance)
On-chip detection performance

Applications

This technology holds transformative potential for:

  • Early disease screening (e.g., Hepatitis A/E)
  • Personalized medicine
  • Clinical diagnostics
    Compared to ELISA, e-DOF drastically reduces sample volume and detection time, enabling ​​rapid, label-free, multiplexed detection​​.

Core Equipment Support

The study deployed ​​Optoseeker’s DropletBot® Digital Microfluidics System​​ to achieve unprecedented detection efficiency and sensitivity. This innovation promises broad applications in disease diagnostics, drug development, and POCT, delivering transformative solutions for clinical practice.

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