平板式数字 PCR 结构的多因素耦合热模拟

Qixuan Li, Xulei Qin, Haoyu Wang
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引用次数: 0

摘要

为了使平板数字聚合酶链式反应(dPCR)达到均匀的反应温度,我们提出了一种利用有限元分析对平板数字 PCR 结构进行多因素耦合热模拟的方法。这将有助于我们获得平板式数字聚合酶链反应结构的最佳方法。热模拟分析了强制风冷、热电冷却器(TEC)排列间距和导热板厚度对平板式 dPCR 温度均匀性的影响。得出的等温面和速度大小矢量用于总结每个因素的影响。研究发现,在加热期间保持每分钟 3000 转 (RPM) ±10 % 的机械风扇速度可使导热板表面温度的标准偏差降低 29.3 %。此外,当 TEC 间距在 2 毫米至 3.5 毫米之间时,导热板表面温度的标准偏差降低了 87.1 % 至 93.4 %。当隔热板的厚度在 3.5 毫米到 4.5 毫米之间时,隔热板表面温度的标准偏差约为 0.006。通过对隔热板表面温度进行取样分析得出的实验结果与模拟结果一致。这证明该方法在确定 dPCR 结构参数以提高温度均匀性方面具有参考价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-factor coupled thermal simulation of flat-panel digital PCR structure
To achieve uniform reaction temperature in flat-plate digital polymerase chain reaction (dPCR), we propose a multi-factor coupled thermal simulation method for the structure of flat-plate digital PCR using finite element analysis. This will help us obtain the optimal method for the structure of flat-plate dPCR. Thermal simulations were conducted to analyze the effects of forced air cooling, thermoelectric cooler (TEC) arrangement spacing, and heat-conducting plate thickness on the temperature uniformity of the flat-plate dPCR. The resulting isothermal surfaces and velocity magnitude vectors were used to summarize the impact of each factor. The study found that maintaining a mechanical fan speed of 3000 revolutions per minute (RPM) ±10 % during the heating period resulted in a 29.3 % reduction in the standard deviation of the temperature on the surface of the heat-conducting plate. Additionally, when the TEC spacing was between 2 mm and 3.5 mm, the standard deviation of the temperature on the plate's surface decreased by 87.1 % to 93.4 %. When the thickness of the thermal plate ranges from 3.5 mm to 4.5 mm, the standard deviation of the temperature on the surface of the thermal plate varies by approximately 0.006. The experimental results, obtained by sampling and analyzing the temperature on the surface of the thermal plate, are consistent with the simulation results. This proves that the method is informative in determining the structural parameters of the dPCR to enhance temperature uniformity.
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