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将微机电系统技术与芯片实验室相结合:用于数字DNA定量和多重检测的纳升规模硅微腔阵列

Fusing MEMS technology with lab-on-chip: nanoliter-scale silicon microcavity arrays for digital DNA quantification and multiplex testing.

作者信息

Podbiel Daniel, Laermer Franz, Zengerle Roland, Hoffmann Jochen

机构信息

Robert Bosch GmbH, Corporate Sector Research, Microsystems and Nanotechnologies, Robert-Bosch-Campus 1, 71272 Renningen, Germany.

IMTEK - Department of Microsystems Engineering, University of Freiburg Georges-Koehler-Allee 103, 79110 Freiburg, Germany.

出版信息

Microsyst Nanoeng. 2020 Oct 5;6:82. doi: 10.1038/s41378-020-00187-1. eCollection 2020.

Abstract

We report on the development of a microfluidic multiplexing technology for highly parallelized sample analysis via quantitative polymerase chain reaction (PCR) in an array of 96 nanoliter-scale microcavities made from silicon. This PCR array technology features fully automatable aliquoting microfluidics, a robust sample compartmentalization up to temperatures of 95 °C, and an application-specific prestorage of reagents within the 25 nl microcavities. The here presented hybrid silicon-polymer microfluidic chip allows both a rapid thermal cycling of the liquid compartments and a real-time fluorescence read-out for a tracking of the individual amplification reactions taking place inside the microcavities. We demonstrate that the technology provides very low reagent carryover of prestored reagents < 6 × 10 and a cross talk rate < 1 × 10 per PCR cycle, which facilitate a multi-targeted sample analysis via geometric multiplexing. Furthermore, we apply this PCR array technology to introduce a novel digital PCR-based DNA quantification method: by taking the assay-specific amplification characteristics like the limit of detection into account, the method allows for an absolute gene target quantification by means of a statistical analysis of the amplification results.

摘要

我们报告了一种微流控多重技术的开发情况,该技术用于在由硅制成的96个纳升规模微腔阵列中通过定量聚合酶链反应(PCR)进行高度并行的样品分析。这种PCR阵列技术具有完全自动化的等分微流控技术、在高达95°C的温度下强大的样品分隔能力,以及在25 nl微腔内对试剂进行特定应用的预存储功能。本文展示的硅-聚合物混合微流控芯片既允许液体隔室进行快速热循环,又能进行实时荧光读出,以跟踪微腔内发生的单个扩增反应。我们证明该技术提供了极低的预存储试剂残留率<6×10,每个PCR循环的串扰率<1×10,这有助于通过几何多重分析进行多靶点样品分析。此外,我们应用这种PCR阵列技术引入了一种基于数字PCR的新型DNA定量方法:通过考虑检测限等特定检测的扩增特性,该方法允许通过对扩增结果进行统计分析来进行绝对基因靶点定量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69ef/8433415/05ac4d877abf/41378_2020_187_Fig1_HTML.jpg

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