Nanoliter Lab-on-a-Chip for Rapid Parallel Immunoassays

Information

  • Research Project
  • 7109995
  • ApplicationId
    7109995
  • Core Project Number
    R43CA114993
  • Full Project Number
    1R43CA114993-01A2
  • Serial Number
    114993
  • FOA Number
  • Sub Project Id
  • Project Start Date
    7/1/2006 - 18 years ago
  • Project End Date
    6/30/2007 - 17 years ago
  • Program Officer Name
    GIOVANNI, MARIA Y.
  • Budget Start Date
    7/1/2006 - 18 years ago
  • Budget End Date
    6/30/2007 - 17 years ago
  • Fiscal Year
    2006
  • Support Year
    1
  • Suffix
    A2
  • Award Notice Date
    6/28/2006 - 18 years ago

Nanoliter Lab-on-a-Chip for Rapid Parallel Immunoassays

[unreadable] DESCRIPTION (provided by applicant): The development of clinically effective cancer vaccines requires reliable analytical methods to evaluate the immune response to vaccination. Immunoassays are among the most sensitive and specific analytical methods that have been used widely in cancer vaccine research, most commonly to monitor the release of cytokines from T-cells in response to vaccination. A typical immunoassay done in a microtiter plate or antibody microarrays, requires 1-5 hours for just the incubation step (during which the binding processes occur) depending on the actual assay. The total reaction time can be much longer depending on the degree of automation. In a research setting where expensive robotic systems are not affordable, a skilled technician performs several key steps in an immunoassay and the technician time is typically more than half the assay cost. This is particularly true when samples cannot be batched for analysis and require immediate attention. A longer assay time therefore adds to the cost of the assay. Human error due to repeated manual intervention is also a major source of inter-assay and intra-assay variation. The emerging concept of a lab-on-a-chip is uniquely positioned to address these issues, by reducing analysis times and providing high levels of automation to increase the productivity in a lab. Due to the limitations in versatility and functionality in the state-of-the-art microchannel-based lab-on-a-chips, we developed an alternative paradigm for microfluidic manipulation based on electrowetting-actuated nanodroplets. In this phase I proposal we will evaluate the feasibility of fully-automated heterogeneous immunoassays on our lab-on-a-chip platform, on nanoliters of sample. We will develop a sandwich ELISA protocol and test it by assaying for cytokine in clinical samples. In phase II, we will optimize the ELISA protocol and integrate multiple immunoassays and process cells on the same platform. Our eventual goal is to develop a nanoliter, rapid, fully automated, hand-held point-of-analysis/point-of-care analyzer that integrates clinical chemistry, molecular diagnostics, and immunoassays. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R43
  • Administering IC
    CA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    159902
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    394
  • Ed Inst. Type
  • Funding ICs
    NCI:159902\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    ADVANCED LIQUID LOGIC
  • Organization Department
  • Organization DUNS
    140695474
  • Organization City
    RESEARCH TRIANGLE PARK
  • Organization State
    NC
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    277094025
  • Organization District
    UNITED STATES