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Digital Microfluidic Magnetic Separation for Particle-Based Immunoassays

机译:基于微粒的免疫分析的数字微流控磁分离

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摘要

We introduce a new format for particle-based immunoassays relying on digital microfluidics (DMF) and magnetic forces to separate and resuspend antibody-coated paramagnetic particles. In DMF, fluids are electrostatically controlled as discrete droplets (picoliters to microliters) on an array of insulated electrodes. By applying appropriate sequences of potentials to these electrodes, multiple droplets can be manipulated simultaneously and various droplet operations can be achieved using the same device design. This flexibility makes DMF well-suited for applications that require complex, multistep protocols such as immunoassays. Here, we report the first particle-based immunoassay on DMF without the aid of oil carrier fluid to enable droplet movement (i.e., droplets are surrounded by air instead of oil). This new format allowed the realization of a novel on-chip particle separation and resuspension method capable of removing greater than 90% of unbound reagents in one step. Using this technique, we developed methods for noncompetitive and competitive immunoassays, using thyroid stimulating hormone (TSH) and 17β-estradiol (E2) as model analytes, respectively. We show that, compared to conventional methods, the new DMF approach reported here reduced reagent volumes and analysis time by 100-fold and 10-fold, respectively, while retaining a level of analytical performance required for clinical screening. Thus, we propose that the new technique has great potential for eventual use in a fast, low-waste, and inexpensive instrument for the quantitative analysis of proteins and small molecules in low sample volumes.
机译:我们引入了一种新的格式,用于基于颗粒的免疫分析,该分析依赖于数字微流控(DMF)和磁力来分离和重悬抗体包被的顺磁性颗粒。在DMF中,将流体作为离散液滴(皮升至微升)静电控制在一系列绝缘电极上。通过向这些电极施加适当的电势序列,可以同时操纵多个液滴,并且可以使用相同的设备设计来实现各种液滴操作。这种灵活性使DMF非常适合需要复杂,多步骤方案的应用,例如免疫测定。在这里,我们报告了在DMF上的第一个基于颗粒的免疫测定方法,该方法无需借助油载流体就能使液滴运动(即液滴被空气而不是油包围)。这种新格式可以实现一种新颖的芯片上颗粒分离和再悬浮方法,该方法能够一步去除90%以上的未结合试剂。使用这项技术,我们开发了用于非竞争性和竞争性免疫测定的方法,分别使用甲状腺刺激激素(TSH)和17β-雌二醇(E2)作为模型分析物。我们证明,与传统方法相比,此处报道的新DMF方法将试剂体积和分析时间分别减少了100倍和10倍,同时保持了临床筛查所需的分析性能水平。因此,我们认为,这项新技术在快速,低浪费,廉价的仪器中最终用于低样品量蛋白质和小分子的定量分析方面具有巨大的潜力。

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