SBIR Phase I: High Throughput COVID-19 Testing
- Funded by National Science Foundation (NSF)
- Total publications:0 publications
Grant number: 2037653
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Key facts
Disease
COVID-19Start & end year
20212021Known Financial Commitments (USD)
$254,536Funder
National Science Foundation (NSF)Principal Investigator
William BrewerResearch Location
United States of AmericaLead Research Institution
Dpx Technologies, LlcResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Diagnostics
Special Interest Tags
N/A
Study Type
Unspecified
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Not Applicable
Vulnerable Population
Not applicable
Occupations of Interest
Not applicable
Abstract
The broader impact of this Small Business Innovation Research (SBIR) Phase I project is faster turnaround time for coronavirus disease 2019 (COVID-19) testing results. Routine testing of nasopharyngeal swabs are being performed globally to try to control the spread of the virus. Ideally, the results of this testing will be done and reported within 24 hours, preferably less. Unfortunately, testing results have commonly been taking 2-3 days or even longer due to case backlogs. Successful development of the technology from this research should ensure much faster reporting of results by reducing the primary bottleneck of sample preparation of COVID-19 testing. In addition, this research should greatly improve the ability to analyze saliva samples by rapidly enriching the ribonucleic acid (RNA) of the virus, and this should therefore lead to greatly reducing false negative results (especially for pooled samples). The proposed project utilizes a patent pending membrane device for rapidly automating sample extraction. The use of these devices allows for samples to be introduced under vacuum, and RNA to be enriched in less than 10 min. The extracts can be rapidly dispensed into multiple 96 or possibly 384 well plates for high throughput analysis. The enriched RNA from nasopharyngeal swabs or saliva will be ready for sensitive analysis using polymerase chain reaction (PCR).