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Droplet-based biochemical assay by magnetic wire manipulation between multiple droplets

机译:通过多个液滴之间的电磁线操作进行基于液滴的生化测定

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摘要

Reaction performance of a droplet-based biochemical assay technique that uses magnetic wires as sample carriers is evaluated. Wires 2.0 mm in length, 0.05 mm in width, and 0.02 mm in thickness are fabricated by chemical etching, introduced into a droplet immersed in oil, and manipulated by the magnetic force of a moving magnet. Alkaline-phosphatase as an enzyme is immobilized on the wire surfaces by applying Au and self-assembled monolayer coatings, and the method's on-chip reaction performance is evaluated. The enzymatic reaction is found to increase linearly as the number of wires and the reaction time increase. Relatively high performance reproducibility for enzymatic reactions is obtained; on average, the reaction absorbance, standard deviation, and coefficient of variance are found to be respectively 1.14, 0.103, and 9.1%. The conductivity change in a fused droplet is used to evaluate the absolute volume of liquid transferred with the extracted wires and a value of 0.33 μl is obtained.
机译:评估了使用磁线作为样品载体的基于液滴的生化分析技术的反应性能。通过化学蚀刻来制造长度为2.0mm,宽度为0.05mm,厚度为0.02mm的电线,将其引入浸入油中的液滴中,并通过移动磁体的磁力进行操纵。通过应用Au和自组装单层涂层将碱性磷酸酶作为酶固定在金属丝表面,并评估该方法的片上反应性能。发现酶反应随线数和反应时间的增加而线性增加。获得了相对较高的酶促反应再现性;平均而言,反应吸光度,标准偏差和方差系数分别为1.14、0.103和9.1%。熔融液滴中的电导率变化用于评估随提取导线传输的液体的绝对体积,并且获得的值为0.33μl。

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