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Device Structure for enhancement of DNA hybridization kinetics by Electrodeless Dielectrophoresis

Published online by Cambridge University Press:  01 February 2011

Nathan Swami
Affiliation:
nswami@virginia.edu, University of Virginia, Electrical & Computer Engineering, 351 McCormick Rd., PO Box 400743, Charlottesville, VA, 22904, United States
Chia-fu Chou
Affiliation:
cfchou@phys.sinica.edu.tw, Academia Sinica, Institute of Physics, 128, Sec. 2, Academia Rd., Nankang, Taipei, 11529, Taiwan
Fernanda Camacho-Alanis
Affiliation:
fac5u@virginia.edu, University of Virginia, Electrical & Computer Engineering, 351 McCormick Rd., PO Box 400743, Charlottesville, VA, 22904, United States
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Abstract

Signal transduction for purposes of biomolecular sensing can be enhanced through miniaturization (nanoscale sensors such as nanowires, cantilevers, etc), but this may impose insurmountable limitations on transport of analyte molecules to the surface. In order to improve biomolecular detection sensitivity, this study aims to develop electrodeless dielectrophoresis (EDEP) methods for the selective transport and trapping of analytes in close proximity to the sensor surface. A device design based on microscale dielectric constrictions of the fluidic channel and nanoscale metal electrode edges was used to locally enhance electric field gradients and trap biomolecules. The resulting electric field focusing effect was enhanced as a result of miniaturization and an instantaneous ten-fold EDEP preconcentration was obtained in high-salt buffers (50 mM NaCl) that enabled an equivalent improvement in DNA hybridization kinetics.

Type
Research Article
Copyright
Copyright © Materials Research Society 2008

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References

REFERENCES

[1] Bishop, J., Chagovetz, A., Blair, S., Nanotechnology, 17, 24422448 (2006).Google Scholar
[2] Sheehan, P. E., Whitman, L. J., Nano Letters, 5, 803807 (2005).Google Scholar
[3] Brolo, A. G., Arctander, E., Gordon, R., Leathem, B., Kavanagh, K. L., Nano Letters, 4, 20152018 (2004)..Google Scholar
[4] Yonzon, C. R., Jeoungf, E., Zou, S. L., Schatz, G. C., Mrksich, M., Duyne, R. P. Van, J. Am. Chem. Soc., 126, 1266912676 (2004).Google Scholar
[5] Rindzevicius, T., Alaverdyan, Y., Dahlin, A., Hook, F., Sutherland, D. S., Kall, M., Nano Letters, 5, 23352339 (2005).Google Scholar
[6] Cao, Y. W. C., Jin, R. C., Mirkin, C. A., Science, 297, 15361540 (2002).Google Scholar
[7] Chou, C. F., Tegenfeldt, J. O., Bakajin, O., Chan, S. S., Cox, E. C., Darnton, N., Duke, T., Austin, R. H., Biophysical Journal, 83, 21702179 (2002).Google Scholar
[8] Swami, N., Chou, C.F., Terbrueggen, R., “Two-potential electrochemical probe for study of DNA immobilization”, Langmuir, 21, 19371941 (2005).Google Scholar