Literature DB >> 22240904

Locally enhanced concentration and detection of oligonucleotides in a plug-based microfluidic device.

Wei-Feng Fang1, Shang-Chieh Ting, Ching-Wen Hsu, Yu-Tzu Chen, Jing-Tang Yang.   

Abstract

We propose a novel technique that allows oligonucleotides with specific end-modification within a plug in a plug-based microfluidic device to undergo a locally enhanced concentration at the rear of the plug as the plug moves downstream. DNA was enriched and detected in situ upon exploiting a combined effect underlain by an entropic force induced through fluid shear (i.e. a hydrodynamic-repellent effect) and the interfacial adsorption (aqueous/oil interface) attributed to affinity. Flow fields within a plug were visualized quantitatively using micro-particle image velocimetry (micro-PIV); the distribution of the fluid shear strain rate explains how the hydrodynamic-repellent effect engenders a dumbbell-like region with an increased concentration of DNA. The concentration of FAM (6-carboxy-fluorescein)-labeled DNA (FC-DNA) and of TAMRA (tetramethyl-6-carboxyrhodamine)-labeled DNA (TC-DNA), respectively, and the hybridization of probe DNA (modified with FAM) with target DNA (modified with TAMRA) were investigated in devices; a confocal fluorescence microscope (CFM) was utilized to monitor the processes and to resolve the corresponding 2D patterns and 3D reconstruction of the DNA distribution in a plug. TC-DNA, but not FC-DNA, concentrating within a plug was affected by the combined effect so as to achieve a concentration factor (C(r)) twice that of FC-DNA because of the lipophilicity of TAMRA. Using fluorescence resonance-energy transfer (FRET), we characterized the hybridization of the DNA in a plug; the detection limit of a system, improved by virtue of the proposed technique (the locally enhanced concentration), for DNA detection was estimated to be 20-50 nM. This technique enables DNA to concentrate locally in a nL-pL free-solution plug, the locally enhanced concentration to profit the hybridization efficiency and the detection of DNA, prospectively serving as a versatile means to accomplish a rapid DNA detection in a small volume for a Lab-on-a-Chip (LOC) system.

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Year:  2012        PMID: 22240904     DOI: 10.1039/c2lc20917a

Source DB:  PubMed          Journal:  Lab Chip        ISSN: 1473-0189            Impact factor:   6.799


  4 in total

1.  A Laplace pressure based microfluidic trap for passive droplet trapping and controlled release.

Authors:  Melinda G Simon; Robert Lin; Jeffrey S Fisher; Abraham P Lee
Journal:  Biomicrofluidics       Date:  2012-02-24       Impact factor: 2.800

2.  LCAT pump optimization for an integrated microfluidic droplet generator.

Authors:  Wei-Feng Fang; Abraham P Lee
Journal:  Microfluid Nanofluidics       Date:  2015-02-04       Impact factor: 2.529

3.  Rapid and continuous magnetic separation in droplet microfluidic devices.

Authors:  Eric Brouzes; Travis Kruse; Robert Kimmerling; Helmut H Strey
Journal:  Lab Chip       Date:  2015-02-07       Impact factor: 6.799

Review 4.  Microfluidic Devices for Forensic DNA Analysis: A Review.

Authors:  Brigitte Bruijns; Arian van Asten; Roald Tiggelaar; Han Gardeniers
Journal:  Biosensors (Basel)       Date:  2016-08-05
  4 in total

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