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Ultrafast DNA Amplification Using Microchannel Flow-Through PCR Device. | LitMetric

Ultrafast DNA Amplification Using Microchannel Flow-Through PCR Device.

Biosensors (Basel)

Master and PhD Program in Biotechnology Industry, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan.

Published: May 2022

AI Article Synopsis

  • PCR is limited by long reaction times, currently taking 30-40 minutes, mainly due to slow heating and cooling, rather than the chemical reactions themselves.
  • The study introduces an ultrafast PCR platform using microchannel chips that can complete 40 thermal cycles in under 3 minutes, demonstrating effective heat conduction with a channel height of 56 μm.
  • The microfluidic design allows for rapid DNA extension at approximately 60 base-pairs per second and achieves a detection limit of 67 copies, highlighting its potential for commercial ultrafast PCR applications.

Article Abstract

Polymerase chain reaction (PCR) is limited by the long reaction time for point-of-care. Currently, commercial benchtop rapid PCR requires 30−40 min, and this time is limited by the absence of rapid and stable heating and cooling platforms rather than the biochemical reaction kinetics. This study develops an ultrafast PCR (<3 min) platform using flow-through microchannel chips. An actin gene amplicon with a length of 151 base-pairs in the whole genome was used to verify the ultrafast PCR microfluidic chip. The results demonstrated that the channel of 56 μm height can provide fast heat conduction and the channel length should not be short. Under certain denaturation and annealing/extension times, a short channel design will cause the sample to drive slowly in the microchannel with insufficient pressure in the channel, causing the fluid to generate bubbles in the high-temperature zone and subsequently destabilizing the flow. The chips used in the experiment can complete 40 thermal cycles within 160 s through a design with the 56 µm channel height and with each thermal circle measuring 4 cm long. The calculation shows that the DNA extension speed is ~60 base-pairs/s, which is consistent with the theoretical speed of the Klen Taq extension used, and the detection limit can reach 67 copies. The heat transfer time of the reagent on this platform is very short. The simple chip design and fabrication are suitable for the development of commercial ultrafast PCR chips.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138433PMC
http://dx.doi.org/10.3390/bios12050303DOI Listing

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