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Ultrafast plasmonic and real-time label-free polymerase chain reaction

机译:超快等离子和实时无标记聚合酶链反应

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There is a growing focus to adapt Polymerase Chain Reaction (PCR) to point-of-care (POC) testing to provide for a lowcost,rapid and reliable diagnostic instrument. Many studies proposed the integration of microfluidics with fluorophoreassistedor electrochemical amplicon detection methods to introduce a real-time miniature device for POC applications.However, their practicality in POC testing is limited due to their complex microfabrication, high cost, and intrinsicchallenges due to their intercalation and hybridization-based detection. In this paper, we present a purely opticalmethodology without the addition of non-PCR reagents (electroactive or fluorogenic DNA intercalators) to enhance thereliability in quantitative PCR measurement of DNA yield. The determination of PCR results and DNA ampliconquantification are realized by monitoring transmitted power of a 260nm LED in PCR reaction at every thermal cycle. Theleast-square fits to transmission data demonstrate distinctive features to classify positive vs. negative PCRs and to quantifyamplified products. This real-time UV monitoring system was combined with a VCSEL-based plasmonic thermocycler toaccomplish fast amplification and detection in a simple and small-scaled footprint applicable for POC diagnostics.
机译:人们越来越关注使聚合酶链反应(PCR)适应即时检验(POC)测试,以提供低成本, 快速可靠的诊断仪器。许多研究提出将微流体与荧光团辅助整合 或电化学扩增子检测方法,以引入用于POC应用的实时微型设备。 然而,由于其复杂的微加工,高成本和固有的特性,它们在POC测试中的实用性受到限制。 由于它们的插入和基于杂交的检测而带来的挑战。在本文中,我们提出了一种纯粹的光学 无需添加非PCR试剂(电活性或荧光DNA嵌入剂)的方法 DNA产量定量PCR测量的可靠性。 PCR结果和DNA扩增子的确定 通过在每个热循环中监测PCR反应中260nm LED的发射功率来实现定量。这 传输数据的最小二乘拟合显示出区分正反PCR和定量PCR的独特功能 扩增产物。该实时紫外线监控系统与基于VCSEL的等离激元热循环仪相结合,可用于 可以在适用于POC诊断的简单且小规模的封装中完成快速的扩增和检测。

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