SBIR/STTR Research Award
SBIR Phase I: Ultra-Sensitive and Multiplexed Pathogen Profiling for Neonatal Sepsis Detection
Award amount
$298,646Program and phase
SBIR · Phase IAward year
2025Award details
- Awarding agency
- National Science Foundation
- Branch
- Not reported
- Recipient company
- ANVIL DIAGNOSTICS INC.
- Proposal award date
- 2025-01-14
- Contract end date
- 2025-09-30
- UEI
- FTUHMF9LM4H1
- Solicitation number
- NSF 24-579
- Topic code
- BM
Research abstract
The broader impact/commercial potential of this Small Business Innovation Research (SBIR) Phase I project lies in its potential to transform sepsis diagnostics and patient care, particularly for vulnerable newborns. Globally, sepsis is responsible for up to a third of neonatal deaths, with an increased burden in low- and middle- income countries. Current diagnostic methods rely heavily on blood cultures, which require substantial blood volumes, take 24+ hours to yield results, and frequently produce false negatives. The proposed DNA-based technology seeks to comprehensively identify and quantify pathogens in a few hours from small volumes of blood, critical capabilities for low-birthweight and immunocompromised newborns. The clinical impacts could include more targeted antibiotic therapy and guided therapy durations that could translate to thousands of lives saved annually, shortened hospital stays, and reduced readmission rates. This technology's compatibility with existing digital PCR hardware enables a very capital-efficient development path and reduces barriers to adoption in hospitals given the expanding use of digital PCR in clinical diagnostic laboratories. Enabling routine pathogen testing for sepsis in any community hospital represents a major opportunity. The core proposed technologies can build on a growing installed base of compatible hardware, adding new tests in other diverse applications.
This Small Business Innovation Research (SBIR) Phase I project aims to develop a rapid diagnostic test for sepsis-causing pathogens in plasma samples with available digital PCR hardware that can scale to cover all critical pathogens. Pathogen identification tests must be very sensitive, fast, and able to detect a wide range of organisms. Specific innovations are proposed to make the test suitable for neonates with less than 1 mL of blood per test. Currently, digital PCR-based technologies achieve state-of-the-art sensitivity with results in a few hours but are lim
Technology keywords
Not reported