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Characterization of DNA hybridization kinetics in a microfluidic flow channel. | LitMetric

Characterization of DNA hybridization kinetics in a microfluidic flow channel.

Sens Actuators B Chem

Department of Mechanical and Aerospace Engineering, University of California, Irvine, CA 92697, USA.

Published: January 2006

AI Article Synopsis

  • - This study investigates how various factors like flow rate, velocity, DNA concentration, channel height, and time affect the process of DNA hybridization in microfluidics.
  • - Using a syringe pump, the researchers sent Cy3-labeled target DNA through a PDMS microfluidic channel to bind with DNA from the West Nile Virus.
  • - They found that lowering the channel height improves the delivery of target DNA to capture probes, leading to higher fluorescence for lower DNA concentrations, with optimal results achieved at a high flow rate and low channel height in just 2 minutes.

Article Abstract

In this investigation we report on the influence of volumetric flow rate, flow velocity, complementary DNA concentration, height of a microfluidic flow channel and time on DNA hybridization kinetics. A syringe pump was used to drive Cy3-labeled target DNA through a polydimethylsiloxane (PDMS) microfluidic flow channel to hybridize with immobilized DNA from the West Nile Virus. We demonstrate that a reduction of channel height, while keeping a fixed volumetric flow rate or a fixed flow velocity, enhances mass transport of target DNA to the capture probes. Compared to a passive hybridization, the DNA hybridization in the microfluidic flow channel generates higher fluorescence intensities for lower concentration of target DNA during the same fixed period of time. Within a fixed 2 min time period the fastest DNA hybridization at a 50 pM concentration of target DNA is achieved with a continuous flow of target DNA at the highest flow rate and the lowest channel height.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125766PMC
http://dx.doi.org/10.1016/j.snb.2005.03.034DOI Listing

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