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A High-Voltage SOI CMOS Exciter Chip for a Programmable Fluidic Processor System | IEEE Journals & Magazine | IEEE Xplore

A High-Voltage SOI CMOS Exciter Chip for a Programmable Fluidic Processor System


Abstract:

A high-voltage (HV) integrated circuit has been demonstrated to transport fluidic droplet samples on programmable paths across the array of driving electrodes on its hydr...Show More

Abstract:

A high-voltage (HV) integrated circuit has been demonstrated to transport fluidic droplet samples on programmable paths across the array of driving electrodes on its hydrophobically coated surface. This exciter chip is the engine for dielectrophoresis (DEP)-based micro-fluidic lab-on-a-chip systems, creating field excitations that inject and move fluidic droplets onto and about the manipulation surface. The architecture of this chip is expandable to arrays of N X N identical HV electrode driver circuits and electrodes. The exciter chip is programmable in several senses. The routes of multiple droplets may be set arbitrarily within the bounds of the electrode array. The electrode excitation waveform voltage amplitude, phase, and frequency may be adjusted based on the system configuration and the signal required to manipulate a particular fluid droplet composition. The voltage amplitude of the electrode excitation waveform can be set from the minimum logic level up to the maximum limit of the breakdown voltage of the fabrication technology. The frequency of the electrode excitation waveform can also be set independently of its voltage, up to a maximum depending upon the type of droplets that must be driven. The exciter chip can be coated and its oxide surface used as the droplet manipulation surface or it can be used with a top-mounted, enclosed fluidic chamber consisting of a variety of materials. The HV capability of the exciter chip allows the generated DEP forces to penetrate into the enclosed chamber region and an adjustable voltage amplitude can accommodate a variety of chamber floor thicknesses. This demonstration exciter chip has a 32 x 32 array of nominally 100 V electrode drivers that are individually programmable at each time point in the procedure to either of two phases: 0deg and 180deg with respect to the reference clock. For this demonstration chip, while operating the electrodes with a 100-V peak-to-peak periodic waveform, the maximum HV electrode wave...
Published in: IEEE Transactions on Biomedical Circuits and Systems ( Volume: 1, Issue: 2, June 2007)
Page(s): 105 - 115
Date of Publication: 05 November 2007

ISSN Information:

PubMed ID: 23851665
References is not available for this document.

I. Introduction

As microelectronics fabrication technology scaling and integrated device performance improve, the realization of a “laboratory on a chip” for chemical and fluid analysis becomes more feasible. A microscale fluidic analysis device could be portable, robust and durable, store samples and chemicals in well controlled spaces that have reduced exposure to environmental contamination, use highly accurate metering of small quantities of reagents and samples, be time efficient through parallel processing, and be cost efficient with small-quantity sample and chemical usage. The hardware may be of a disposable or a reusable type. It could provide wider availability of valuable diagnostic tools, reduce costs of chemicals and samples due to volume scaling, and provide versatility by testing multiple agents with a generic fluidic analyzer type.

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1.
P. Gascoyne, J. Vykoukal, J. Schwartz, T. Anderson, D. Vykoukal, K. W. Current, et al., "Dielectrophoresis-based programmable fluidic processors", Lab on a Chip, vol. 4, pp. 299-309, 2004.
2.
N. Manaresi, A. Romani, G. Medoro, L. Altomare, A. Leonardi, M. Tartagni, et al., "A CMOS chip for individual cell manipulation and detection", IEEE J. Solid-State Circuits, vol. 38, no. 12, pp. 2297-2305, Dec. 2003.
3.
J. R. Keilman, G. A. Jullien and K. V. I. S. Kaler, "A SoC bio-analysis platform for real-time biological cell analysis-on-a-chip", Proc. IEEE 3rd Int. Workshop System-on-Chip for Real-Time Appl., pp. 362-368, 2003.
4.
Y. Li and K. V. I. S. Kaler, "DEP based cell separation utilizing planar microelectrode array", Proc. IEEE 2002 Ann. Rep. Conf. Electr. Insul. Dielectric Phenom., pp. 680-684, 2002.
5.
J. Vykoukal, J. Schwartz, F. Becker and P. Gascoyne, "A programmable dielectrophoretic fluid processor for droplet-based chemistry", Proc. Micro Total Anal. Syst., pp. 12-1A, 2001.
6.
P. Gascoyne, X. Wang, Y. Huang and F. Becker, "Dielectrophoretic separation of cancer cells from blood", IEEE Trans. Indust. Appl., vol. 33, no. 3, pp. 670-678, May-Jun. 1997.
7.
K. W. Current, K. Yuk, C. McConaghy, P. Gascoyne, J. Schwartz, J. Vykoukal, et al., "A high-voltage CMOS VLSI programmable fluidic processor chip", Proc. 2005 VLSI Circuits Symp., pp. 72-75, 2005-Jun.
8.
K. W. Current, K. Yuk, C. McConaghy, P. Gascoyne, J. Schwartz, J. Vykoukal, et al., "A high-voltage integrated circuit engine for a dielectrophoresis-based programmable microfluidic processor", Proc. Int. Conf. MEMS Nano Smart Syst., pp. 153-158, 2005-Jul.
9.
A. Enteshari, G. A. Jullien, O. Yadid-Pecht and K. V. I. S. Kaler, "All CMOS low power platform for dielectrophoresis bio-analysis", Proc. 31st Eur. Solid-State Circuits Conf, pp. 339-342, 2005.
10.
A. Romani, N. Manaresi, L. Marzocchi, G. Medoro, A. Leonardi, L. Altomare, et al., "Capacitive sensor array for localization of bioparticles in CMOS lab-on-a-chip", Proc. IEEE Int. Solid-State Circuits Conf. Dig. Techn. Papers, pp. 224-225, 2004-Feb.
11.
E. J. Griffith, S. Akella and M. K. Goldberg, "Performance characterization of a reconfigurable planar-array digital microfluidic system", IEEE Trans. Computer-Aided Des. Integr. Circuits Syst., vol. 25, no. 2, pp. 345-357, Feb. 2006.
12.
J. A. Schwartz, J. V. Vykoukal and P. R. C. Gascoyne, "Droplet-based chemistry on a programmable microchip", Lab on a Chip, vol. 4, pp. 11-17, 2004.
13.
J. A. Schwartz, Dielectrophoretic Approaches to Sample Preparation and Analysis, Dec. 2001.

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References

References is not available for this document.