分析物
有孔小珠
色谱法
检出限
微流控
化学
免疫分析
微珠(研究)
电泳
分析化学(期刊)
材料科学
纳米技术
抗体
免疫学
复合材料
生物化学
生物
作者
Yuri M. Shlyapnikov,Elena A. Shlyapnikova
出处
期刊:Biosensors
[Multidisciplinary Digital Publishing Institute]
日期:2025-05-15
卷期号:15 (5): 316-316
摘要
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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