SBIR-STTR Award

High-Content Label-Free Electro-Optic Surface Plasmon Resonance Assay Platform
Award last edited on: 9/20/13

Sponsored Program
SBIR
Awarding Agency
NIH : NIGMS
Total Award Amount
$126,130
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Ernest F Guignon

Company Information

Ciencia Inc (AKA: Techquest Inc)

111 Roberts Street Suite K
East Hartford, CT 06108
   (860) 528-9737
   info@ciencia.com
   www.ciencia.com
Location: Single
Congr. District: 01
County: Hartford

Phase I

Contract Number: 1R43GM104636-01
Start Date: 9/1/12    Completed: 2/28/13
Phase I year
2012
Phase I Amount
$126,130
The objective of this Phase I SBIR proposal is the development of a novel instrumentation platform based on Surface Plasmon Resonance (SPR) that if validated would greatly increase the utility of this label-free technology to researchers utilizing high-content assays in systems biology investigations. The benefits of this platform derive from a change in detection paradigm that permits solid-state measurements of SPR shifts as a function of voltage. By moving away from an angle-scanning or wavelength-scanning approach, the proposed proprietary electro-optic grating-coupled SPR platform (EOSPR) would investigate changes in bound mass at as many as 100,000 regions of interest simultaneously. The sensitivity increase over current instrumentation is expected to improve over current label-free state-of-the-art in that data collection will be significantly more rapid in the proposed systm than in other high-content devices. The inclusion of additional data into the averaged measurement implies a greater signal-to-noise ratio, but further advantages are available to the EOSPR system that would not be viable in other SPR platforms. A signal-chopping scheme that could only be implemented on a system that scans as rapidly as the EOSPR device is expected to reduce the noise of the instrumentation. The combination of better signal and reduced noise is expected to lead to increases in label- free detection sensitivity that could approach that of label-based techniques. In addition, since scans of the SPR curves could be completed much more rapidly than in classic devices, the direct measure of more rapid binding events becomes possible. The steps that will be required to verify if this technology can be turned into a commercial product include: modeling of the proposed chip, fabrication the chip, modifying an existing SPR instrument that was previously designed by Ciencia, and conducting proof-of-concept experiments on the prototype system. The objectives to meet these tasks are outlined within the body of this proposal, and strategic consulting arrangements and subcontracts will be employed to maximize the possibility of success for this potentially high-impact project.

Public Health Relevance:
Current trends in biomedical research imply that the future of medicine will rely upon ever-increasing degrees of personalized therapy. As the number of understood disease states and therapeutic options increase, so does the amount of diagnostic information necessary to make an informed decision. The proposed EOSPR technology aims to aid systems biology researchers in elucidating and understanding these complex molecular mechanisms by filling the need for a sensitive, label-free, and high-content assay that is affordable enough for widespread adoption.

Public Health Relevance Statement:
Current trends in biomedical research imply that the future of medicine will rely upon ever-increasing degrees of personalized therapy. As the number of understood disease states and therapeutic options increase, so does the amount of diagnostic information necessary to make an informed decision. The proposed EOSPR technology aims to aid systems biology researchers in elucidating and understanding these complex molecular mechanisms by filling the need for a sensitive, label-free, and high-content assay that is affordable enough for widespread adoption.

NIH Spending Category:
Bioengineering; Biotechnology

Project Terms:
Adoption; Atomic Force Microscopy; Attention; base; Binding (Molecular Function); Biological Assay; Biomedical Research; Complex; Consult; cost; cost effective; Coupled; Data; Data Collection; design; Detection; detector; Development; Devices; Diagnostic; Dimensions; Disease; Encapsulated; Equation; Event; Future; Gold; Housing; Imaging technology; improved; Industry; innovation; instrument; instrumentation; interest; Investigation; Label; Lasers; Lead; Location; Marketing; Measurement; Measures; Mechanics; Medicine; meetings; metabolomics; Microarray Analysis; Modeling; Modification; Molecular; Nature; Nickel; Noise; novel; Optics; Pattern; Phase; Polymers; Property; Proteomics; prototype; Reaction; Refractive Indices; Research; Research Personnel; research study; Resolution; response; Scanning; Scheme; Signal Transduction; Small Business Innovation Research Grant; solid state; Solutions; Spottings; Staging; success; Surface; Surface Plasmon Resonance; System; Systems Biology; Techniques; Technology; Telecommunications; Testing; Theoretical Studies; Therapeutic; Time; trend; Validation; voltage

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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