SBIR/STTR Research Award

Bringing PFAS Monitoring Home: An Integrated Magnetic Nanoparticle and Lateral Flow Assay System

Award identifier 4eb6fbc28ca5e1917bced76c17077d21240708f0fd21e3546c5f7418522bffc7Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$306,789

Program and phase

SBIR · Phase I

Award year

2025

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
BIOTA INC.
Proposal award date
2025-08-01
Contract end date
2026-01-31
UEI
MAPWDAVC9JL7
Solicitation number
PA24-245
Topic code
NIEHS

Research abstract

PROJECT SUMMARY/ABSTRACT Per- and polyƲuoroalkyl substances (PFAS) are persistent environmental contaminants linked to severe health issues, including thyroid dysfunction, cancer, and developmental toxicity. Detected in the blood of 97% of Americans, PFAS exposure poses a critical public health challenge, prompting the EPA to establish stringent regulatory limits for their presence in drinking water. Current PFAS testing methods are prohibitively expensive, time- consuming, and difficult to interpret, creating an urgent need for a rapid, low-cost, and user-friendly solution. This project aims to develop the flrst at-home lateral Ʋow assay (LFA) for PFAS detection, offering a biologically relevant measure of thyroid hormone disruption caused by PFAS. The innovative approach leverages the competition between PFAS and thyroxine (T4) for binding to transthyretin (TTR), providing a toxicity index that correlates exposure with potential health impacts. To achieve sensitivity at the parts-per-trillion (ppt) level required by EPA standards, the test will integrate a novel magnetic nanoparticle pre-concentration method. Three speciflc aims will guide this work: (1) develop and optimize a lateral Ʋow assay utilizing T4-FITC and TTR protein to quantify PFAS concentrations as a function of thyroid hormone disruption, (2) create functionalized silica nanoparticles capable of achieving a 1000-fold PFAS concentration efficiency, and (3) reflne a nanoparticle elution buffer that is compatible with the TTR-T4 assay, enabling future integration into an at-home, user-friendly diagnostic device. The combined nanoparticle pre-concentration step and lateral Ʋow assay will be validated using water samples spiked with PFOA or PFAS at concentrations ranging from 1 ppt to 10 ppb, assessing sensitivity, performance, and dynamic range under realistic conditions. Phase I aims to establish proof-of-concept for a high- performance, accessible environmental diagnostic. Future Phase II efforts will focus on integrating the nanoparticle pre-concentration and lateral Ʋow assay into a single, scalable device optimized for affordability and use by non- experts. This project aligns with the mission of advancing public health through innovative diagnostic technologies, enabling consumers to monitor and mitigate PFAS exposure. Upon completion, this technology will redeflne environmental monitoring, enhance consumer health tools, and generate critical data linking PFAS exposure to health outcomes.

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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