BioPrism: An optical nanoparticle sorting assay

Information

  • Research Project
  • 8523232
  • ApplicationId
    8523232
  • Core Project Number
    R43EB015797
  • Full Project Number
    1R43EB015797-01A1
  • Serial Number
    015797
  • FOA Number
    PA-10-150
  • Sub Project Id
  • Project Start Date
    7/1/2013 - 11 years ago
  • Project End Date
    6/30/2014 - 10 years ago
  • Program Officer Name
    KORTE, BRENDA
  • Budget Start Date
    7/1/2013 - 11 years ago
  • Budget End Date
    6/30/2014 - 10 years ago
  • Fiscal Year
    2013
  • Support Year
    01
  • Suffix
    A1
  • Award Notice Date
    6/21/2013 - 11 years ago
Organizations

BioPrism: An optical nanoparticle sorting assay

DESCRIPTION: Optofluidics Inc. proposes to develop a novel protein-binding assay platform called the BioPrism. The Bioprism is a multiplexable, label-free, bead-based binding assay. The system will be ideal for in vitro molecular diagnostics, therapeutic development and molecular biology research. The need for more cost-effective high throughput assays is ever present in the pharmaceutical industry, which routinely tests millions of compounds in an effort to find a single effective drug ($19.9B Market by 2017). Molecular binding assays are the basis of the booming biomarker in-vitro diagnostics field ($20B in the US by 2014). There are several highly multiplexed bead-based platforms in the market, but these systems require secondary labels which are expensive and add steps to the assay. There are also successful commercial systems that do label-free protein binding measurements; however they have very little or no multiplexing capability. We propose to combine the best elements from both systems into the BioPrism. The BioPrism will use nanoscale optical devices (photonics) developed in the Erickson Lab at Cornell University and currently being commercialized by Optofluidics. Using a microfluidic flow cell, into which a bead-laden sample is injected, the platform can distinguish between bare nanobeads and protein-bound nanobeads using size- based photonic separation. Protein coated nanobeads significantly increase in size due to the small volume of the starting nanobead. By starting with fluorescent nanoparticles of different colors, where each color corresponds to a different probe, the method can be easily multiplexed. The size of the bead will determine whether analytes have bound and the fluorescence of the bead indicates which probe captured a target. In this Phase I project, we will manufacture our BioPrism chips, characterize the system using off-the-shelf nanoparticles, carry out binding assays to detect the binding of mouse IgG and carry out numerical simulations on the device design to optimize performance. In Phase II, we will focus on assay development and the design and construction of a shippable BioPrism system.

IC Name
NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING
  • Activity
    R43
  • Administering IC
    EB
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    99841
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    286
  • Ed Inst. Type
  • Funding ICs
    NIBIB:99841\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    OPTOFLUIDICS, INC.
  • Organization Department
  • Organization DUNS
    963268151
  • Organization City
    Philadelphia
  • Organization State
    PA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    191045504
  • Organization District
    UNITED STATES