4.8 Article

Electrokinetically Driven Exosome Separation and Concentration Using Dielectrophoretic-Enhanced PDMS-Based Microfluidics

Journal

ANALYTICAL CHEMISTRY
Volume 91, Issue 23, Pages 14975-14982

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.9b03448

Keywords

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Funding

  1. School of Engineering and Science at Tecnologico de Monterrey through the Bioprocess Focus Group [0020209I13, 0020209I06]
  2. FEMSA-Biotechnology Center at Tecnologico de Monterrey through the Bioprocess Focus Group [0020209I13, 0020209I06]
  3. National Council on Science and Technology of Mexico (CONACyT) [493963]
  4. School of Engineering and Science at Tecnologico de Monterrey through the Nanosensors and Devices Focus Group [0020209I13, 0020209I06]
  5. FEMSA-Biotechnology Center at Tecnologico de Monterrey through the Nanosensors and Devices Focus Group [0020209I13, 0020209I06]

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Exosomes are a specific subpopulation of extracellular vesicles that have gained interest because of their many potential biomedical applications. However, exosome isolation and characterization are the first steps toward designing novel applications. This work presents a direct current-insulator-based dielectrophoretic (DC-iDEP) approach to simultaneously capture and separate exosomes by size. To do so, a microdevice consisting of a channel with two electrically insulating post sections was designed. Each section was tailored to generate different nonuniform spatial distributions of the electric field and, therefore, different dielectrophoretic forces acting on exosomes suspended in solution. Side channels were placed adjacent to each section to allow sample recovery. By applying an electric potential difference of 2000 V across the length of the main channel, dielectrophoretic size-based separation of exosomes was observed in the device. Analysis of particle size in each recovered fraction served to assess exosome separation efficiency. These findings show that iDEP can represent a first step toward designing a high-throughput, fast, and robust microdevice capable of capturing and discriminating different subpopulations of exosomes based on their size.

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