UCLA researchers in the Department of Mechanical and Aerospace Engineering have developed a novel device for high-throughput label-free analysis of cells.
Cytometry is an essential analytical tool in cell biology and disease diagnosis and has an estimated market size of over $6.3 billion by 2020. While many flow techniques require fluorescent tags, labeling requires additional handling as well as the presence of specific antibodies or markers on the cells of interest. One label-free technique is electrorotation (ROT), where the rotation of a cell in a magnetic field can be correlated to its characteristic dielectric properties. In conventional ROT, cells must be carefully positioned so each receives the same electric field strength for accurate comparison. However, this presents significant challenges at the single-cell level and results may be affected by friction between the cell and the surrounding medium. Novel high throughput methods of isolating and analyzing cells using ROT would significantly improve the label-free analysis of cells.
Professor Chiou and coworkers have developed a novel microfluidic device for high throughput analysis of cells using electrorotation (ROT). Using dielectrophoresis (DEP), cells are aligned and focused within a tunnel-shaped electric field. A second set of electrical signals is then applied to rotate the focused cells and a high-speed camera is used to image the rotating cells. Post-processing analysis enables the measurement of cell size, texture, shape, and rotation speed. This technique does not require fluorescent labeling and flow throughput in the device is improved by 4 orders of magnitude compared to conventional electrorotation-based cell analysis, up to 42 cells/sec.
Devices have been fabricated and shown to separate leukemia, lymphoma, and cervical cancer cells.
Microfluidic, flow cytometry, electrorotation, cell analysis, cellular biophysics, microchannel flow, electrorotation flow, continuous flow, focusing, single-cell analysis, plastic, substrates