4.6 Article

Nucleic Acid Detection with Ion Concentration Polarization Microfluidic Chip for Reduced Cycle Numbers of Polymerase Chain Reaction

Journal

MICROMACHINES
Volume 13, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/mi13091394

Keywords

microfluidic; nucleic acid detection; polymerase chain reaction; electrokinetic preconcentration; ion concentration polarization

Funding

  1. National Natural Science Foundation of China [51728502]
  2. Fund for Distinguish Young Scholars in Tianjin 2018 3rd Round [180191]
  3. Hebei Science and Technology Foundation [19271707D]
  4. Hebei Natural Science Foundation [E2022202127, E2020202101, F2021202001]
  5. Department of Human Resources and Social Security of Hebei Province [C20200314, C20210337]
  6. Jiangsu Key Laboratory of Advanced Manufacturing Equipment and Technology [FMZ202016]

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A rapid nucleic acid detection method was developed in this study, using PCR and ICP technology combined with Nafion film for enrichment. The capability of the method was demonstrated through an animal-derived component detection experiment for meat product identification applications, with a detection time of about 35 min.
Nucleic acid detection is widely used in disease diagnosis, food safety, environmental monitoring and many other research fields. The continuous development of rapid and sensitive new methods to detective nucleic acid is very important for practical application. In this study, we developed a rapid nucleic-acid detection method using polymerase chain reaction (PCR) combined with electrokinetic preconcentration based on ion concentration polarization (ICP). Using a Nafion film, the proposed ICP microfluidic chip is utilized to enrich the nucleic acid molecules amplified by PCR thermal cycles. To demonstrate the capability of the microfluidic device and the hybrid nucleic-acid detection method, we present an animal-derived component detection experiment for meat product identification applications. With the reduced cycle numbers of 24 cycles, the detection can be completed in about 35 min. The experimental results show that this work can provide a microfluidic device and straightforward method for rapid detection of nucleic acids with reduced cycle numbers.

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