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Microfluidic magnetic fluidized bed for DNA analysis in continuous flow mode

机译:用于连续流动模式下DNA分析的微流体流化床

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AbstractMagnetic solid phase substrates for biomolecule manipulation have become a valuable tool for simplification and automation of molecular biology protocols. However, the handling of magnetic particles inside microfluidic chips for miniaturized assays is often challenging due to inefficient mixing, aggregation, and the advanced instrumentation required for effective actuation. Here, we describe the use of a microfluidic magnetic fluidized bed approach that enables dynamic, highly efficient and simplified magnetic bead actuation for DNA analysis in a continuous flow platform with minimal technical requirements. We evaluate the performance of this approach by testing the efficiency of individual steps of a DNA assay based on padlock probes and rolling circle amplification. This assay comprises common nucleic acid analysis principles, such as hybridization, ligation, amplification and restriction digestion. We obtained efficiencies of up to 90% for these reactions with high throughput processing up to 120μL of DNA dilution at flow rates ranging from 1 to 5μL/min without compromising performance. The fluidized bed was 20–50% more efficient than a commercially available solution for microfluidic manipulation of magnetic beads. Moreover, to demonstrate the potential of this approach for integration into micro-total analysis systems, we optimized the production of a low-cost polymer based microarray and tested its analytical performance for integrated single-molecule digital read-out. Finally, we provide the proof-of-concept for a single-chamber microfluidic chip that combines the fluidized bed with the polymer microarray for a highly simplified and integrated magnetic bead-based DNA an
机译:<![cdata [ 抽象 用于生物分子操纵的磁性固相衬底已成为分子生物学协议的简化和自动化的有价值的工具。然而,由于有效的混合,聚集和有效致动所需的先进仪器,微流体芯片内的微流体芯片内的磁性颗粒的处理通常是挑战。在这里,我们描述了使用微流体磁化床方法的使用,使得能够在连续流平台中进行动态,高效和简化的磁珠致动,具有最小的技术要求。通过基于挂锁探针和滚动圆扩增测试DNA测定的单个步骤的效率,我们评估这种方法的性能。该测定包括常见的核酸分析原理,例如杂交,结扎,扩增和限制消化。我们获得了高达90%的效率,这些反应高达90μl,在不损害性能的情况下以1至5μL/ min的流速为120μlDNA稀释。流化床比市售的磁珠的微流体操纵更有效地高出20-50%。此外,为了证明这种方法集成到微量分析系统中的潜力,我们优化了生产低成本的基于聚合物的微阵列,并测试了其分析性能的集成单分子数字读出。最后,我们为单室微流体芯片提供了概念的证据,该概念与聚合物微阵列将流化床与聚合物微阵列相结合,以获得高度简化和集成的磁珠基DNA

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