Smartphone-based POC Testing for HIV Using Glowstick Chemistry
Project Number5R61AI174294-03
Contact PI/Project LeaderWILLSON, RICHARD
Awardee OrganizationUNIVERSITY OF HOUSTON
Description
Abstract Text
Effective testing for HIV allows for detection of acute infections (new and rebound), appropriate
antiretroviral treatment, suppression of viral load, and interruption of transmission. However, early
detection of infection or regular self-monitoring at point-of-need or at home remains a challenge. Lateral
flow assays are a well-established, inexpensive point-of-need diagnostic method, and commonly are
favored when applicable because of their ease of use and low cost. Where they most commonly fall
short is in analytical sensitivity, notably in antigen-detection diagnostics for infectious diseases. Our
goal is to develop radically-improved LFAs by implementing the inexpensive, shelf-stable
chemi-excitation chemistry of glow sticks in a point-of-care format to excite fluors without light or optical
filters. Our preliminary results suggest this chemistry enables LFAs with greatly improved limits of
detection (very low pg/mL), using a standard smartphone with a $2 adaptor and no sophisticated optical
components. Our central hypothesis is that our novel, reagent-optimized chemi-excited lateral flow
assay technology integrated with a storage-stable reagent cartridge and readable with a smartphone
will lead to a new, widely-useful and potentially very-superior class of highly-sensitive lateral flow
assays. We will test this hypothesis through 5 specific aims: (1) Development of a highly-sensitive and
easily-usable lateral flow assay for HIV p24 in human blood, including development of novel
avidity-enhanced dual-fibronectin-domain binders, (2) Immune complex dissociation (ICD) for
rebound/breakthrough HIV diagnosis, (3) Testing with 300 negative and archived-positive human
samples from diverse cohorts, (4) To evaluate clinical performance using fresh samples from patients
and usability with a diverse population of subjects at high risk of HIV infection/rebound (R33 Phase), (5)
Easier usability by more people, quality assurance for test items (R33 Phase).
Public Health Relevance Statement
This proposal aims to advance a new platform for high-sensitivity, point-of-care lateral flow assays to allow
users to test themselves for HIV infection and rebound. Accurate, frequent HIV self-testing can facilitate early
detection of HIV infection and rebound, allowing early treatment and decreasing transmission.
National Institute of Allergy and Infectious Diseases
CFDA Code
855
DUNS Number
036837920
UEI
QKWEF8XLMTT3
Project Start Date
06-January-2023
Project End Date
31-December-2025
Budget Start Date
01-January-2025
Budget End Date
31-December-2025
Project Funding Information for 2025
Total Funding
$392,731
Direct Costs
$287,080
Indirect Costs
$105,651
Year
Funding IC
FY Total Cost by IC
2025
National Institute of Allergy and Infectious Diseases
$242,731
2025
National Institute on Drug Abuse
$150,000
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R61AI174294-03
Publications
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Patents
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Outcomes
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No Outcomes available for 5R61AI174294-03
Clinical Studies
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History
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