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Droplet centrifugation droplet DNA extraction and rapid droplet thermocycling for simpler and faster PCR assay using wire-guided manipulations

机译:液滴离心液滴DNA提取和快速液滴热循环可通过线引导操作进行更简单更快速的PCR测定

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摘要

A computer numerical control (CNC) apparatus was used to perform droplet centrifugation, droplet DNA extraction, and rapid droplet thermocycling on a single superhydrophobic surface and a multi-chambered PCB heater. Droplets were manipulated using “wire-guided” method (a pipette tip was used in this study). This methodology can be easily adapted to existing commercial robotic pipetting system, while demonstrated added capabilities such as vibrational mixing, high-speed centrifuging of droplets, simple DNA extraction utilizing the hydrophobicity difference between the tip and the superhydrophobic surface, and rapid thermocycling with a moving droplet, all with wire-guided droplet manipulations on a superhydrophobic surface and a multi-chambered PCB heater (i.e., not on a 96-well plate). Serial dilutions were demonstrated for diluting sample matrix. Centrifuging was demonstrated by rotating a 10 μL droplet at 2300 round per minute, concentrating E. coli by more than 3-fold within 3 min. DNA extraction was demonstrated from E. coli sample utilizing the disposable pipette tip to cleverly attract the extracted DNA from the droplet residing on a superhydrophobic surface, which took less than 10 min. Following extraction, the 1500 bp sequence of Peptidase D from E. coli was amplified using rapid droplet thermocycling, which took 10 min for 30 cycles. The total assay time was 23 min, including droplet centrifugation, droplet DNA extraction and rapid droplet thermocycling. Evaporation from of 10 μL droplets was not significant during these procedures, since the longest time exposure to air and the vibrations was less than 5 min (during DNA extraction). The results of these sequentially executed processes were analyzed using gel electrophoresis. Thus, this work demonstrates the adaptability of the system to replace many common laboratory tasks on a single platform (through re-programmability), in rapid succession (using droplets), and with a high level of accuracy and automation.
机译:使用计算机数控(CNC)设备在单个超疏水表面和多腔PCB加热器上执行液滴离心,液滴DNA提取和快速液滴热循环。使用“线引导”方法(本研究中使用移液器吸头)操作液滴。此方法可以轻松地适应现有的商用机器人移液系统,同时还展示了附加功能,例如振动混合,液滴的高速离心,利用尖端和超疏水表面之间的疏水性差异的简单DNA提取以及移动时的快速热循环液滴,全部在超疏水性表面和多腔PCB加热器上(即,不在96孔板上)通过线引导液滴操纵。证明了连续稀释可以稀释样品基质。通过以每分钟2300转的速度旋转10μL液滴,在3分钟内将大肠杆菌浓缩3倍以上来证明离心。用一次性移液器吸头从大肠杆菌样品中证明了DNA的提取,巧妙地吸引了来自超疏水表面上的液滴的提取DNA,该过程耗时不到10分钟。提取后,使用快速液滴热循环扩增大肠杆菌的肽酶D的1500 bp序列,该过程需时10分钟,持续30循环。整个测定时间为23分钟,包括液滴离心,液滴DNA提取和快速液滴热循环。在这些程序中,从10μL液滴中蒸发并不明显,因为最长的时间暴露于空气中并且振动少于5分钟(在DNA提取过程中)。使用凝胶电泳分析这些顺序执行的过程的结果。因此,这项工作证明了该系统具有适应性,能够以高连续性(使用液滴)并以高水平的准确性和自动化来替换单个平台上的许多常见实验室任务(通过重新编程)。

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