Rolosense: An innovative platform for automatic mobile phone readout of active SARS-CoV-2 particles (RADx-rad / SEED Administrative Supplement)

  • Funded by National Institutes of Health (NIH)
  • Total publications:0 publications

Grant number: 3U01AA029345-02S1

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2022.0
    2024.0
  • Known Financial Commitments (USD)

    $500,000
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    ASSOCIATE PROFESSOR Khalid Salaita
  • Research Location

    United States of America
  • Lead Research Institution

    EMORY UNIVERSITY
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Diagnostics

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

Project summary: The supplement application is in response to the RADx-rad announcement on the opportunity of additional resources and funding support to facilitate the pathway to commercialization. As part of this supplement we will pursue specific milestones to de-risk the Rolosense technology and further move it toward commercialization. A major goal will be to introduce multiplexing capabilities to simultaneously detect multiple viral targets from the same sample. Encoded Rolosense particles with unique virus-binding ligands will be employed to achieve this goal. Multiplexing to detect multiple viral targets will help distinguish the capabilities of Rolosense from that of the current state-of-the-art. Another goal is to increase the speed and robustness of the assay to facilitate direct sensing from breath condensate samples. This second goal will be pursued by further developing fuel-free Rolosense that eliminates the need for RNA and RNaseH enzyme in the assay. We see this as a critical step to reduce the cost of the assay and to increase rigor and reproducibility to achieve the commercialization goals without concern for RNaseA found in most biological samples.