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纳米等离子体芯片 PCR 用于快速精准分子诊断。

Nanoplasmonic On-Chip PCR for Rapid Precision Molecular Diagnostics.

机构信息

Department of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea.

KAIST Institute for Health Science and Technology (KIHST), Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2020 Mar 18;12(11):12533-12540. doi: 10.1021/acsami.9b23591. Epub 2020 Mar 6.

DOI:10.1021/acsami.9b23591
PMID:32101396
Abstract

Emerging molecular diagnosis requires ultrafast polymerase chain reaction (PCR) on chip for rapid precise detection of infectious diseases in the point-of-care test. Here, we report nanoplasmonic on-chip PCR for rapid precision molecular diagnostics. The nanoplasmonic pillar arrays (NPA) comprise gold nanoislands on the top and sidewall of large-scale glass nanopillar arrays. The nanoplasmonic pillars enhance light absorption of a white light-emitting diode (LED) over the whole visible range due to strong electromagnetic hotspots between the nanoislands. As a result, they effectively induce photothermal heating for ultrafast PCR thermal cycling. The temperature profile of NPA exhibits 30 cycles between 98 and 60 °C for a total of 3 min and 30 s during the cyclic excitation of white LED light. The experimental results also demonstrate the rapid DNA amplification of both 0.1 ng μL of λ-DNA in 20 thermal cycles and 0.1 ng μL of complementary DNA of Middle East respiratory syndrome coronavirus in 30 thermal cycles using a conventional PCR volume of 15 μL. This nanoplasmonic PCR technique provides a new opportunity for rapid precision molecular diagnostics.

摘要

新兴的分子诊断需要在芯片上进行超快速聚合酶链反应 (PCR),以便在即时护理测试中快速准确地检测传染病。在这里,我们报告了用于快速精确分子诊断的纳米等离子体芯片上 PCR。纳米等离子体柱阵列 (NPA) 由大尺寸玻璃纳米柱阵列的顶部和侧壁上的金纳米岛组成。纳米等离子体柱由于纳米岛之间的强电磁场热点,在整个可见光谱范围内增强了白光发光二极管 (LED) 的光吸收。因此,它们有效地诱导用于超快 PCR 热循环的光热加热。NPA 的温度曲线在白光 LED 光的循环激发下,在 98 和 60°C 之间进行 30 个循环,总共 3 分 30 秒。实验结果还表明,使用传统的 15μL PCR 体积,在 20 个热循环中可以快速扩增 0.1ngμL 的 λ-DNA,在 30 个热循环中可以快速扩增中东呼吸综合征冠状病毒的 0.1ngμL 互补 DNA。这种纳米等离子体 PCR 技术为快速精确的分子诊断提供了新的机会。

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