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首页> 外文期刊>Analytical chemistry >On-Chip Enzyme Immunoassay of a Cardiac Marker Using a Microfluidic Device Combined with a Portable Surface Plasmon Resonance System
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On-Chip Enzyme Immunoassay of a Cardiac Marker Using a Microfluidic Device Combined with a Portable Surface Plasmon Resonance System

机译:使用微流控设备结合便携式表面等离子体共振系统的心脏标记物的片上酶免疫测定

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This paper reports a miniaturized immunosensor designed to determine a trace level cardiac marker, B-type natriuretic peptide (BNP), using a microfluidic device combined with a portable surface plasmon resonance (SPR) sensor system. Sample BNP solution was introduced into the microchannel after an immunoreaction with acetylcholine esterase-labeled antibody (conjugate), and only unbound conjugate was trapped on the BNP-immobilized surface in the flow channel. Then, the thiol compound generated by the enzymatic reaction with the trapped conjugate was accumulated on a gold thin film located downstream in the microchannel to monitor the real-time SPR angle shift. We achieved a detectable concentration range of 5 pg/mL-100 ng/mL by monitoring the SPR angle shift, which covers the required detection range for the BNP concentrations found in blood. This success resulted from the use of a T-shaped microfluidic device structure, which prevents the sample solution from flowing over the gold film used for SPR detection. We were able to measure trace levels of BNP peptide (15 fg) within 30 min since the procedure with our immunosensor is simpler than a multistep immunoassay through the simultaneous use of a labeled enzymatic reaction and the real-time monitoring of enzymatic product accumulation in the microfluidic device. We employed the procedure to detect serum BNP by using spiked samples in human serum and achieved satisfactory recovery for heat-treated samples to denature the esterase in the serum before the immunoreaction.
机译:本文报道了一种微型免疫传感器,该传感器设计为使用微流体装置结合便携式表面等离子体共振(SPR)传感器系统来确定痕量心脏标志物B型利钠肽(BNP)。在与乙酰胆碱酯酶标记的抗体(结合物)进行免疫反应后,将样品BNP溶液引入微通道,并且只有未结合的结合物被捕获在流动通道中BNP固定的表面上。然后,通过与捕获的共轭物的酶促反应产生的硫醇化合物被堆积在位于微通道下游的金薄膜上,以监测实时SPR角位移。通过监测SPR角偏移,我们达到了5 pg / mL-100 ng / mL的可检测浓度范围,该范围涵盖了血液中BNP浓度所需的检测范围。这种成功是由于使用了T形微流控设备的结构,该结构可防止样品溶液流过用于SPR检测的金膜。我们能够在30分钟内测量痕量的BNP肽(15 fg),因为通过同时使用标记的酶促反应和实时监测酶催化产物的积聚,我们的免疫传感器比多步免疫测定更简单。微流体装置。我们采用该程序通过使用人血清中的加标样品检测血清BNP,并在免疫反应之前对热处理过的样品变性了血清中的酯酶,获得了令人满意的回收率。

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