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声流耦合的声流酶联免疫吸附测定(ELISA)平台。

Acoustofluidic enzyme-linked immunosorbent assay (ELISA) platform enabled by coupled acoustic streaming.

机构信息

C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV, USA.

C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV, USA.

出版信息

Anal Chim Acta. 2019 Nov 4;1079:129-138. doi: 10.1016/j.aca.2019.05.073. Epub 2019 Jun 1.

Abstract

Bead-based ELISA in microfluidics is a promising platform for reducing the reagent consumption and improving assay throughput due to its fast binding kinetics and low reagent consumption. Current microfluidic bead-based immunoassay mainly relies on magnetic and centrifugal forces to manipulate microparticles to complete an assay protocol. Here we report an acoustic streaming-based microfluidic method that can perform all the fluid and particle operations of bead-based ELISA. A series of sharp-edge structures are used to generate a long-range coupled acoustic streaming that enables simultaneous particle trapping and active molecular exchange in a dead-end microchannel. The device achieved >99% of molecular exchange in 4 min, while maintaining a particle trapping efficiency of 85%. This acoustofluidic-based method demonstrates all three key operations in a bead-based immunoassay: (1) Beads "immobilization"; (2) Active mixing of fluid for bead/target binding; (3) Active molecular exchange for reagent loading and washing. Finally, on-chip quantitative detection of biomarker IL-6 with a limit of detection ∼50 pg/mL is achieved using this platform including an enzymatic signal amplification step. The small footprint, simple setup, and continuous flow operation of the acoustic streaming-based method makes it an attractive platform for continuous flow bead-based immunoassay.

摘要

基于微珠的酶联免疫吸附分析(Bead-based ELISA)在微流控领域是一种很有前途的平台,由于其快速的结合动力学和低试剂消耗,可减少试剂消耗并提高分析通量。目前的微流控基于微珠的免疫分析主要依赖于磁场和离心力来操纵微珠以完成分析方案。在这里,我们报告了一种基于声流的微流控方法,该方法可以执行基于微珠的 ELISA 的所有流体和颗粒操作。使用一系列锐边结构来产生长程耦合的声流,从而在死端微通道中实现同时捕获微珠和主动分子交换。该器件在 4 分钟内实现了 >99%的分子交换,同时保持 85%的微珠捕获效率。这种基于声流的方法展示了基于微珠的免疫分析中的三个关键操作:(1)微珠“固定化”;(2)用于微珠/靶标结合的主动混合;(3)用于试剂加载和洗涤的主动分子交换。最后,通过此平台(包括酶信号放大步骤)实现了对生物标志物 IL-6 的芯片上定量检测,检测限约为 50 pg/mL。基于声流的方法占地面积小、设置简单且连续流动操作,使其成为连续流动基于微珠的免疫分析的有吸引力的平台。

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