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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Geometric optimisation of electrohydrodynamic fluid flows for enhanced biosensing
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Geometric optimisation of electrohydrodynamic fluid flows for enhanced biosensing

机译:电液动力流体流动的几何优化,用于增强生物传感

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AbstractThe removal of non-specific binding on the sensor surface represents a major challenge for rapid and sensitive biosensing. The stimulation of an electrohydrodynamic (EHD) fluid flow in proximity to the biosensor surface can improve sensor performance. The EHD fluid flow is depending on the geometry of electrodes. Here, the effect of electrode diameter and spacing of asymmetric circular electrodes is investigated for the capability to stimulate fluid flow and capture model beads and protein biomarker. Six geometries with diameters of 30–1000μm and spacing of 200–1500μm were systematically studied. Capture of target beads in excess of non-target beads showed higher target bead capture with increase in electrode diameter. The target bead capture was 4× improved and displacement of non-target reduced by factor 2. The electrode with the highest bead capture was then used to establish an immunoassay for detection of novel cancer immunotherapy biomarker CD28 fortified in buffer and fetal bovine serum. The EHD parameters for optimal CD28 capture were different to the bead capture parameters. This indicated that, depending on the binding strength of target to affinity tag, the EHD parameters could be tailored to provide ideal capture conditions. The use of EHD significantly reduced the assay time by 92.4%, removed non-target binding by a factor of 3.5 compared to static incubation, and was sensitive to detect as low as 20pgmL?1CD28. In a proof-of-concept study, the potential of the EHD-assisted immunoassay for point of care application was demonstrated using a simple naked eye read-out.
机译:<![cdata [ 抽象 在传感器表面上的移除非特异性绑定代表了快速和敏感的生物传感的主要挑战。电液动力学(EHD)流体在邻近生物传感器表面的刺激可以提高传感器性能。 EHD流体流量取决于电极的几何形状。这里,研究了电极直径和不对称圆形电极间距的影响,以刺激流体流动和捕获模型珠粒和蛋白质生物标志物的能力。最直径为30-1000μm的六个几何图,系统地研究了200-1500μm的间距。超过非靶珠的靶珠捕获显示出较高的靶珠捕获,随着电极直径的增加而捕获。靶珠捕获为4倍,无靶的非目标的位移减少了因子2。然后使用具有最高珠捕获的电极来建立用于检测缓冲液和胎儿牛血清中的新型癌症免疫治疗生物标志物CD28的免疫测定。最佳CD28捕获的EHD参数与珠子捕获参数不同。这表明,根据目标对亲和标签的结合强度,可以根据靶的绑定强度,以提供EHD参数以提供理想的捕获条件。与静态孵化相比,EHD的使用显着降低了测定时间92.4%,将非靶结合除去3.5因子,并敏感地检测到20pgml 1 < / ce:sup> cd28。在概念证据研究中,使用简单的肉眼读出证明了EHD辅助免疫测定点的潜力。 < / ce:摘要>

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