4.5 Article

Electrical tweezer for highly parallelized electrorotation measurements over a wide frequency bandwidth

Journal

ELECTROPHORESIS
Volume 35, Issue 12-13, Pages 1795-1802

Publisher

WILEY-BLACKWELL
DOI: 10.1002/elps.201400021

Keywords

Biological cells; Dielectrophoresis; Electrical tweezer; Electrorotation

Funding

  1. Asian Office Aerospace Research Development [114083]
  2. NSF [1332329]
  3. Directorate For Engineering
  4. Emerging Frontiers & Multidisciplinary Activities [1332329] Funding Source: National Science Foundation

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Electrorotation (ROT) is a powerful tool for characterizing the dielectric properties of cells and bioparticles. However, its application has been somewhat limited by the need to mitigate disruptions to particle rotation by translation under positive DEP and by frictional interactions with the substrate. While these disruptions may be overcome by implementing particle positioning schemes or field cages, these methods restrict the frequency bandwidth to the negative DEP range and permit only single particle measurements within a limited spatial extent of the device geometry away from field nonuniformities. Herein, we present an electrical tweezer methodology based on a sequence of electrical signals, composed of negative DEP using 180-degree phase-shifted fields for trapping and levitation of the particles, followed by 90-degree phase-shifted fields over a wide frequency bandwidth for highly parallelized electrorotation measurements. Through field simulations of the rotating electrical field under this wave-sequence, we illustrate the enhanced spatial extent for electrorotation measurements, with no limitations to frequency bandwidth. We apply this methodology to characterize subtle modifications in morphology and electrophysiology of Cryptosporidium parvum with varying degrees of heat treatment, in terms of shifts in the electrorotation spectra over the 0.05-40 MHz region. Given the single particle sensitivity and the ability for highly parallelized electrorotation measurements, we envision its application toward characterizing heterogeneous subpopulations of microbial and stem cells.

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