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Continuous flow layer-by-layer microbead functionalization via a micropost array railing system

机译:通过MicroPost阵列栏杆系统连续流动层逐层微珠官能化

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The ability to achieve multi-layer synthesis on the surface of microbeads is critical for diverse chemical and biological assays. Although microfluidic techniques for layer-by-layer (LbL) synthesis have been demonstrated for droplets, accomplishing continuous flow multi-layer synthesis for microbeads has remained a significant challenge. Here we present a micropost array railing (µPAR) system to achieve continuous flow LbL functionalization on microbead substrates in a microfluidic device. Microposts arrayed at a 1° angle served as a railing system for directing microbeads into adjacent flow streams of bio-molecules and washes. An extended biological linker (including four biotin-avidin pairs) was synthesized onto streptavidin-coated 15-µm diameter polystyrene microbeads via an eight-stage LbL process (with additional wash steps between each reaction). After completion of the biological linker, a fluorescently labeled analyte was bound to the linker and microbead fluorescence was observed.
机译:在微珠表面上实现多层合成的能力对于各种化学和生物测定是至关重要的。虽然已经对逐层(LBL)合成的微流体技术进行了证明用于液滴,但是为微珠完成连续流量的多层合成仍然存在重大挑战。在这里,我们提出了一种微孔阵列栏杆(&#00b5; par)系统,以在微流体装置中实现对微珠基材的连续流动LBL官能化。微孔排列在1&#x00b0处;角度用作栏杆系统,用于将微珠引入生物分子和洗涤的相邻流动流中。通过八级LBL工艺合成将延长的生物接头(包括四种生物素 - 抗生物素对,包括四个µ M直径聚苯乙烯微珠(每次反应之间的额外洗涤步骤)合成。在完成生物接头后,荧光标记的分析物与接头结合,观察到微珠荧光。

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