Collaborative research: development of fbep-enabled electrochemical sensors for heart failure monitoring

The National Science Foundation Division of Electrical, Communications and Cyber Systems awarded $200,000 to the University of Houston on October 1, 2026, for collaborative research developing FBEP-enabled electrochemical sensors for heart failure monitoring under the Engineering program (CFDA 47.041).

The research develops a wearable sensing approach for continuous monitoring of N-terminal pro-B-type natriuretic peptide in skin interstitial fluid as an alternative to intermittent blood draws for heart failure diagnosis, risk assessment, and treatment monitoring. The project establishes an aptamer-based electrochemical platform combining molecular-recognition engineering, electrically controlled sensing, and wearable microneedle technology. Research objectives include developing and optimizing NT-proBNP-binding aptamers with high affinity, selectivity, and stability in biofluids at physiological temperature, and determining how fast biphasic electric pulse waveform parameters and electrochemical readout conditions control signal generation, interface recovery, and sensing bandwidth. The work incorporates project concepts and results into undergraduate and graduate course modules and educational and public outreach activities on wearable biosensors and heart-health monitoring.

The award obligates $200,000 with a period of performance from October 1, 2026, through September 30, 2029. Work is performed at the University of Houston in Houston, Texas. This is a collaborative research project; the source does not detail sub-recipient roles or funding.

Abstract

Heart failure affects millions of americans and is a major cause of hospitalization, disability, and healthcare spending. N-terminal pro-b-type natriuretic peptide (NT-probnp) is widely used to diagnose heart failure, assess risk, and monitor treatment response, but current testing depends primarily on intermittent blood draws that provide only isolated snapshots of a changing disease state. More frequent measurements could reveal rising, falling, or rebound NT-probnp trajectories and support earlier recognition of worsening heart failure or treatment response. This project will develop a less invasive wearable sensing approach for higher-frequency NT-probnp monitoring in skin interstitial fluid. The project serves the national interest by advancing technologies for cardiovascular health, establishing broadly useful principles for continuous monitoring of protein biomarkers, and training students at the intersection of chemistry, electrochemistry, biointerfaces, and biomedical engineering. Project concepts and results will also be incorporated into undergraduate and graduate course modules and into educational and public outreach activities on wearable biosensors and heart-health monitoring that are open and available to all eligible participants. This collaborative project will establish an aptamer-based electrochemical platform that combines molecular-recognition engineering, electrically controlled sensing, and wearable microneedle technology. The research has three interdependent objectives. First, the team will develop and optimize NT-probnp-binding aptamers with high affinity, selectivity, and stability in biofluids at physiological temperature. Second, the team will determine how fast biphasic electric pulse (fbep) waveform parameters and electrochemical readout conditions control signal generation, interface recovery, and sensing bandwidth on standard screen-printed electrodes. These studies will define operating conditions for repeated NT-probnp measurements at substantially higher temporal resolution than conventional affinity-sensing formats. Third, the optimized aptamer?fbep sensing approach will be transferred to miniaturized microneedle sensors incorporating nanoporous gold electrodes and antifouling surface coatings, followed by testing in artificial interstitial fluid, serum, and pilot animal studies. The project is expected to produce an NT-probnp monitoring platform and quantitative design rules for converting aptamer-based protein detection from endpoint measurement into reversible electrochemical continuous monitoring. This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the foundation's intellectual merit and broader impacts review criteria.- subawards are not planned for this award.