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Updated: Feb 11, 2026

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Published on: June 9, 2023
Detection of Multiple Pathogens in Serum Using Silica-Encapsulated Nanotags in a Surface-Enhanced Raman
Jing Neng1, Yina Li1, Ashley J Driscoll1
1Department of Chemical Engineering , University of Wyoming , Laramie , Wyoming 82071 , United States.
A new surface-enhanced Raman scattering (SERS) immunoassay enables simultaneous detection of multiple pathogens like West Nile virus. This sensitive method offers rapid, on-site diagnostics without complex sample preparation.
Area of Science:
- Biotechnology
- Analytical Chemistry
- Immunodiagnostics
Background:
- Accurate and rapid detection of multiple pathogenic antigens is crucial for timely disease diagnosis and monitoring.
- Existing diagnostic methods often require extensive sample preparation and lack the sensitivity or multiplexing capability for complex matrices like serum.
Purpose of the Study:
- To develop a highly sensitive and multiplexed immunoassay for the simultaneous detection of trace amounts of pathogenic antigens.
- To utilize surface-enhanced Raman scattering (SERS) for direct detection in complex biological samples, simplifying sample preparation.
Main Methods:
- Development of a robust immunoassay employing silica-encapsulated nanotags and magnetic nanoparticles conjugated with polyclonal antibodies.
- Utilized magnetic pull-down for immune complex aggregation, followed by SERS detection of distinct spectral fingerprints from captured antigens.
- Tested in 20% fetal bovine serum to assess performance in a complex biological matrix.
Main Results:
- Achieved simultaneous detection of antigens from West Nile virus, Rift Valley fever virus, and Yersinia pestis.
- Established a limit of detection of approximately 10 pg/mL, demonstrating significant improvement in sensitivity.
- Demonstrated enhanced multiplexing capability and reduced complexity compared to previous diagnostic approaches.
Conclusions:
- The developed SERS-based multiplex immunoassay platform offers high sensitivity and specificity for detecting multiple pathogens.
- This method eliminates the need for tedious sample preparation, making it suitable for on-site diagnostic testing.
- Provides a promising tool for real-time disease monitoring and rapid identification of infectious agents directly in crude serum samples.
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