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电动力学分离分析物的按需萃取。

Extraction of electrokinetically separated analytes with on-demand encapsulation.

机构信息

IBM Research - Zurich, Rüschlikon, Switzerland.

Technion - Israel Institute of Technology, Haifa, Israel.

出版信息

Lab Chip. 2018 Dec 7;18(23):3588-3597. doi: 10.1039/c8lc00912k. Epub 2018 Oct 25.

Abstract

Microchip electrokinetic methods are capable of increasing the sensitivity of molecular assays by enriching and purifying target analytes. However, their use is currently limited to assays that can be performed under a high external electric field, as spatial separation and focusing is lost when the electric field is removed. We present a novel method that uses two-phase encapsulation to overcome this limitation. The method uses passive filling and pinning of an oil phase in hydrophobic channels to encapsulate electrokinetically separated and focused analytes with a brief pressure pulse. The resulting encapsulated sample droplet maintains its concentration over long periods of time without requiring an electric field and can be manipulated for further analysis, either on- or off-chip. We demonstrate the method by encapsulating DNA oligonucleotides in a 240 pL aqueous segment after isotachophoresis (ITP) focusing, and show that the concentration remains at 60% of the initial value for tens of minutes, a 22-fold increase over free diffusion after 20 minutes. Furthermore, we demonstrate manipulation of a single droplet by selectively encapsulating amplicon after ITP purification from a polymerase chain reaction (PCR) mix, and performing parallel off-chip detection reactions using the droplet. We provide geometrical design guidelines for devices implementing the encapsulation method, and show how the method can be scaled to multiple analyte zones.

摘要

微芯片电动方法能够通过富集和纯化靶标分析物来提高分子分析的灵敏度。然而,它们的使用目前仅限于可以在高外电场下进行的分析,因为当电场移除时,空间分离和聚焦就会丢失。我们提出了一种新的方法,使用两相封装来克服这一限制。该方法利用油相在疏水性通道中的被动填充和固定来封装电动分离和聚焦的分析物,只需一个短暂的压力脉冲。所得的封装样品液滴在没有电场的情况下长时间保持其浓度,并可用于进一步分析,无论是在芯片上还是在芯片外。我们通过在等速电泳聚焦(ITP)后在 240pL 水相中封装 DNA 寡核苷酸来演示该方法,并表明浓度在数十分钟内保持在初始值的 60%,比 20 分钟后自由扩散时提高了 22 倍。此外,我们通过选择性地在 ITP 从聚合酶链反应(PCR)混合物中纯化后封装扩增子来演示对单个液滴的操纵,并使用该液滴进行并行的芯片外检测反应。我们为实施封装方法的器件提供了几何设计指南,并展示了如何将该方法扩展到多个分析物区域。

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