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Multiscale Design Tools for Non-Homogeneous Microfluidic Biochips with Electronic/Optical Readout

Award Information
Agency: Department of Defense
Branch: Defense Advanced Research Projects Agency
Contract: MDA972-02-C-0017
Agency Tracking Number: 00SB2-0079
Amount: $0.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: N/A
Solicitation Number: N/A
Timeline
Solicitation Year: N/A
Award Year: 2002
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
215 Wynn Drive
Huntsville, AL 35805
United States
DUNS: 185169620
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 Mahesh Athavale
 Group Leader/Research
 (256) 726-4800
 mma@cfdrc.com
Business Contact
 Andrzej Przekwas
Title: Sr. Vice President
Phone: (256) 726-4800
Email: ajp@cfdrc.com
Research Institution
N/A
Abstract

"The overall objective of the project is to develop commercial quality, validated, multi-scale and multi-physics modeling and design tools for macroparticle/cells and macromolecule-laden flows in microdevices under the influence of hydrodynamic, thermal,chemical, AC/DC electric, optical and electromagnetic fields. These tools will provide comprehensive design and optimization support for all components of a biochip system including fluid transport, chemistry and transduction/detection. Themacroparticle-laden flow methodology developed in Phase I will be consolidated, and linked with AC and DC electrical fields for DEP, electrokinetic transport and capacitative detection. Two different methods for optical detection and cell-opticsinteraction will be incorporated: mesh-based electromagnetic field-based method and wave-optics based method. The macroparticle model will be enhanced o include a variety of surface forces: subgrid scale chemical binding, electrostatic, hydrophobic/philicetc., for cell-cell and cell-surface interaction. Reduced scale models for particle flow and detection will be generated from high-fidelity calculations and incorporated in the software for system level calculations of bio-chips. The tools will be linkedwith external software packages to provide hydrodymanic properties of macromolecules/proteins for flow computations. The filament/cluster model will also be extended to simulate motion of large polyelect

* Information listed above is at the time of submission. *

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