Ultrasensitive Bead-Based Immunoassay for Real-Time Continuous Sample Flow Analysis

The performance of heterophase immunoassays is often limited by the kinetics of analyte binding. This problem is partially solved by bead-based assays, which are characterized by rapid diffusion in the particle suspension. However, at low analyte concentrations, the binding rate is still low. Here, we demonstrate a further improvement of analyte binding kinetics in bead-based immunoassays by simultaneously concentrating both an analyte and magnetic beads in a compact spatial region where binding occurs. The analyte is electrophoretically concentrated in a flow cell where beads are magnetically retained and dragged along the channel by viscous force. The flow cell is integrated with a microarray-based signal detection module, where beads with bound analyte scan the microarray surface and are retained on it by single specific interactions, assuring ultra-high sensitivity of the method. Thus, a continuous flow assay system is formed. Its performance is demonstrated by simultaneous detection of model pathogen biomarkers, cholera toxin (CT) and staphylococcal enterotoxin B (SEB), with a detection limit of 0.1 fM and response time of under 10 min. The assay is capable of real-time online sample monitoring, as shown by a 12 h long continuous flow analysis of tap water for SEB and CT.

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Publication Details

Journal
Biosensors
Published
2025-05-15
DOI
https://doi.org/10.3390/bios15050316
Citations
4
Primary Topic
Microfluidic and Capillary Electrophoresis Applications
Type
article
Field-Weighted Citation Impact
2.70
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article

Ultrasensitive Bead-Based Immunoassay for Real-Time Continuous Sample Flow Analysis

Yuri M. Shlyapnikov, Elena A. Shlyapnikova
4 citations
Biosensors
Microfluidic and Capillary Electrophoresis Applications
2.70
article

Ultrasensitive Bead-Based Immunoassay for Real-Time Continuous Sample Flow Analysis

Yuri M. Shlyapnikov, Elena A. Shlyapnikova
article en
4 citations

Abstract

The performance of heterophase immunoassays is often limited by the kinetics of analyte binding. This problem is partially solved by bead-based assays, which are characterized by rapid diffusion in the particle suspension. However, at low analyte concentrations, the binding rate is still low. Here, we demonstrate a further improvement of analyte binding kinetics in bead-based immunoassays by simultaneously concentrating both an analyte and magnetic beads in a compact spatial region where binding occurs. The analyte is electrophoretically concentrated in a flow cell where beads are magnetically retained and dragged along the channel by viscous force. The flow cell is integrated with a microarray-based signal detection module, where beads with bound analyte scan the microarray surface and are retained on it by single specific interactions, assuring ultra-high sensitivity of the method. Thus, a continuous flow assay system is formed. Its performance is demonstrated by simultaneous detection of model pathogen biomarkers, cholera toxin (CT) and staphylococcal enterotoxin B (SEB), with a detection limit of 0.1 fM and response time of under 10 min. The assay is capable of real-time online sample monitoring, as shown by a 12 h long continuous flow analysis of tap water for SEB and CT.

BiosensorsVol. 15(5)
Institute of Theoretical and Experimental Biophysics (RU)
Clean water and sanitation
Openalex Percentile: Top 10%
Microfluidic and Capillary Electrophoresis Applications
2.70
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