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用于数字 PCR 应用的液滴中 DNA 的微流控包封。

Microfluidic encapsulation of DNAs in liquid beads for digital PCR application.

机构信息

Queensland Micro- and Nanotechnology Centre, Griffith University, 170 Kessels Road, Nathan, Queensland 4111, Australia.

出版信息

Analyst. 2023 Aug 21;148(17):4064-4071. doi: 10.1039/d3an00868a.

Abstract

Droplet-based microfluidics and digital polymerase chain reaction (PCR) hold significant promise for accurately detecting and quantifying pathogens. However, existing droplet-based digital PCR (ddPCR) applications have been relying exclusively on single emulsion droplets. Single emulsion droplets may not be suitable for applications such as identifying the source and pathways of water contamination where the templates must be protected against harsh environmental conditions. In this study, we developed a core-shell particle to serve as a protective framework for DNAs, with potential applications in digital PCR. We employed a high-throughput and facile flow-focusing microfluidic device to generate liquid beads, core-shell particles with liquid cores, which provided precise control over process parameters and consequently particle characteristics. Notably, the interfacial interaction between the core and shell liquids could be adjusted without adding surfactants to either phase. As maintaining stability is essential for ensuring the accuracy of digital PCR (dPCR), we investigated parameters that affect the stability of core-shell droplets, including surfactants in the continuous phase and core density. As a proof of concept, we encapsulated a series of human faecal DNA samples in the core-shell droplets and the subsequent liquid beads. The core-shell particles ensure contamination-free encapsulation of DNA in the core. The volume of the core droplets containing the PCR mixture is only 0.12 nL. Our experimental results indicate that the liquid beads formulated using our technique can amplify the encapsulated DNA and be used for digital PCR without interfering with the fluorescence signal. We successfully demonstrated the ability to detect and quantify DNA under varying concentrations. These findings provide new insights and a step change in digital PCR that could benefit various applications, including the detection and tracking of environmental pollution.

摘要

基于液滴的微流控技术和数字聚合酶链反应(PCR)在准确检测和定量病原体方面具有很大的应用前景。然而,现有的基于液滴的数字 PCR(ddPCR)应用一直依赖于单一乳液液滴。单一乳液液滴可能不适合于识别水污染的来源和途径等应用,在这些应用中模板必须免受恶劣环境条件的影响。在本研究中,我们开发了一种核壳粒子作为 DNA 的保护框架,具有在数字 PCR 中的潜在应用。我们采用高通量且简便的流聚焦微流控装置来生成液滴,即具有液芯的核壳粒子,从而可以精确控制工艺参数,进而控制粒子特性。值得注意的是,无需向任何一相添加表面活性剂即可调整核和壳液体之间的界面相互作用。由于维持稳定性对于确保数字 PCR(dPCR)的准确性至关重要,因此我们研究了影响核壳液滴稳定性的参数,包括连续相中的表面活性剂和核密度。作为概念验证,我们将一系列人类粪便 DNA 样品封装在核壳液滴和随后的液滴中。核壳粒子确保了 DNA 在核中的无污染封装。含有 PCR 混合物的核液滴的体积仅为 0.12nL。我们的实验结果表明,使用我们的技术制备的液滴可以扩增封装的 DNA,并可用于数字 PCR,而不会干扰荧光信号。我们成功地证明了在不同浓度下检测和定量 DNA 的能力。这些发现为数字 PCR 提供了新的见解和重大改进,这可能有益于各种应用,包括环境污染的检测和追踪。

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