These authors contributed equally to this work.
Microfluidics and Miniaturization
Selective concentration of human cancer cells using contactless dielectrophoresis†
Article first published online: 26 AUG 2011
DOI: 10.1002/elps.201100081
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

ELECTROPHORESIS
Special Issue: Dielectrophoresis 2011 – Part II
Volume 32, Issue 18, pages 2523–2529, September 2011
Additional Information
How to Cite
Henslee, E. A., Sano, M. B., Rojas, A. D., Schmelz, E. M. and Davalos, R. V. (2011), Selective concentration of human cancer cells using contactless dielectrophoresis. ELECTROPHORESIS, 32: 2523–2529. doi: 10.1002/elps.201100081
- †
- ‡
These authors contributed equally to this work.
Publication History
- Issue published online: 15 SEP 2011
- Article first published online: 26 AUG 2011
- Manuscript Revised: 2 MAY 2011
- Manuscript Accepted: 2 MAY 2011
- Manuscript Received: 27 JAN 2011
Funded by
- Institute for Critical and Applied Sciences (ICTAS) at Virginia Tech, Blacksburg, VA
- Abstract
- Article
- References
- Cited By
Keywords:
- Clausius–Mossotti factor;
- Dielectrophoresis;
- Enrichment;
- Microfluidics;
- Sample isolation
Abstract
This work is the first to demonstrate the ability of contactless dielectrophoresis (cDEP) to isolate target cell species from a heterogeneous sample of live cells. Since all cell types have a unique molecular composition, it is expected that their dielectrophoretic (DEP) properties are also unique. cDEP is a technique developed to improve upon traditional and insulator-based DEP devices by replacing embedded metal electrodes with fluid electrode channels positioned alongside desired trapping locations. Through the placement of the fluid electrode channels and the removal of contact between the electrodes and the sample fluid, cDEP mitigates issues associated with sample/electrode contact. MCF10A, MCF7, and MDA-MB-231 human breast cells were used to represent early, intermediate, and late-staged breast cancer, respectively. Trapping frequency responses of each cell type were distinct, with the largest difference between the cells found at 20 and 30 V. MDA-MB-231 cells were successfully isolated from a population containing MCF10A and MCF7 cells at 30 V and 164 kHz. The ability to selectively concentrate cells is the key to development of biological applications using DEP. The isolation of these cells could provide a workbench for clinicians to detect transformed cells at their earliest stage, screen drug therapies prior to patient treatment, increasing the probability of success, and eliminate unsuccessful treatment options.

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