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用于超快速DNA扩增的印刷电路板上的闭环微反应器:设计与热验证

Closed-Loop Microreactor on PCB for Ultra-Fast DNA Amplification: Design and Thermal Validation.

作者信息

Skaltsounis Panagiotis, Kokkoris George, Papaioannou Theodoros G, Tserepi Angeliki

机构信息

Institute of Nanoscience and Nanotechnology, National Center of Scientific Research (NCSR) "Demokritos", Patr. Gregoriou Ε' and 27 Neapoleos Str., 15341 Aghia Paraskevi, Greece.

School of Medicine, National and Kapodistrian University of Athens (NKUA), 75 Mikras Asias Str., 11527 Athens, Greece.

出版信息

Micromachines (Basel). 2023 Jan 10;14(1):172. doi: 10.3390/mi14010172.

Abstract

Polymerase chain reaction (PCR) is the most common method used for nucleic acid (DNA) amplification. The development of PCR-performing microfluidic reactors (μPCRs) has been of major importance, due to their crucial role in pathogen detection applications in medical diagnostics. Closed loop (CL) is an advantageous type of μPCR, which uses a circular microchannel, thus allowing the DNA sample to pass consecutively through the different temperature zones, in order to accomplish a PCR cycle. CL μPCR offers the main advantages of the traditional continuous-flow μPCR, eliminating at the same time most of the disadvantages associated with the long serpentine microchannel. In this work, the performance of three different CL μPCRs designed for fabrication on a printed circuit board (PCB) was evaluated by a computational study in terms of the residence time in each thermal zone. A 3D heat transfer model was used to calculate the temperature distribution in the microreactor, and the residence times were extracted by this distribution. The results of the computational study suggest that for the best-performing microreactor design, a PCR of 30 cycles can be achieved in less than 3 min. Subsequently, a PCB chip was fabricated based on the design that performed best in the computational study. PCB constitutes a great substrate as it allows for integrated microheaters inside the chip, permitting at the same time low-cost, reliable, reproducible, and mass-amenable fabrication. The fabricated chip, which, at the time of this writing, is the first CL μPCR chip fabricated on a PCB, was tested by measuring the temperatures on its surface with a thermal camera. These results were then compared with the ones of the computational study, in order to evaluate the reliability of the latter. The comparison of the calculated temperatures with the measured values verifies the accuracy of the developed model of the microreactor. As a result of that, a total power consumption of 1.521 W was experimentally measured, only ~7.3% larger than the one calculated (1.417 W). Full validation of the realized CL μPCR chip will be demonstrated in future work.

摘要

聚合酶链反应(PCR)是用于核酸(DNA)扩增的最常用方法。由于其在医学诊断中病原体检测应用中的关键作用,能够进行PCR的微流控反应器(μPCR)的发展具有重要意义。闭环(CL)是一种具有优势的μPCR类型,它使用圆形微通道,从而使DNA样品能够连续通过不同的温度区域,以完成一个PCR循环。CL μPCR具有传统连续流μPCR的主要优点,同时消除了与长蛇形微通道相关的大部分缺点。在这项工作中,通过计算研究评估了三种设计用于在印刷电路板(PCB)上制造的不同CL μPCR在每个热区的停留时间方面的性能。使用三维传热模型计算微反应器中的温度分布,并通过该分布提取停留时间。计算研究结果表明,对于性能最佳的微反应器设计,30个循环的PCR可以在不到3分钟内完成。随后,基于在计算研究中表现最佳的设计制造了一个PCB芯片。PCB是一种很好的基板,因为它允许在芯片内部集成微加热器,同时允许低成本、可靠、可重复和适合大规模制造。所制造的芯片,在撰写本文时,是第一个在PCB上制造的CL μPCR芯片,通过用热成像仪测量其表面温度进行了测试。然后将这些结果与计算研究的结果进行比较,以评估后者的可靠性。计算温度与测量值的比较验证了所开发的微反应器模型的准确性。结果,实验测量的总功耗为1.521 W,仅比计算值(1.417 W)大~7.3%。在未来的工作中将展示所实现的CL μPCR芯片的全面验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/809e/9860919/1b2a2a400718/micromachines-14-00172-g001.jpg

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