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.
Ultrasensitive Bead-Based Immunoassay for Real-Time Continuous Sample Flow Analysis.
用于实时连续样品流动分析的超灵敏微珠免疫分析法
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作者:Shlyapnikov Yuri M, Shlyapnikova Elena A
| 期刊: | Biosensors-Basel | 影响因子: | 5.600 |
| 时间: | 2025 | 起止号: | 2025 May 15; 15(5):316 |
| doi: | 10.3390/bios15050316 | 研究方向: | 免疫/内分泌 |
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