Gale and Jawad Receive UURF Interdisciplinary Research Initiative Track 1 Seed Grant

Munawar Jawad
Bruce Gale
pavlova

Bruce Gale and Munawar Jawad received a UURF Interdisciplinary Research Initiative Track 1 seed grant from the University of Utah Vice President for Research (VPR) Office for a collaborative project focused on point-of-care screening for high-risk human papillomavirus (hrHPV). The project combines microfluidic engineering and molecular assay development to advance a low-cost, accessible diagnostic platform for cervical cancer screening. The work is carried out in collaboration with Natasha Pavlova and her team, with additional industry support from Patrick Manou.

Publication on a Disposable, Passive Microfluidic Cartridge for Antibody Point-of-Care Detection

Munawar Jawad et al. recently published “A disposable, passive microfluidic cartridge for point-of-care detection of antibodies in total capillary blood based on hemagglutination and machine-learning assisted interpretation” in RSC Advances. 

Abstract: Point-of-care (PoC) detection of antibodies in blood enables rapid, on-site diagnosis. However, these devices often face challenges related to user variability due to the requirement of multiple manual operations. To address this issue, we designed and developed a disposable microfluidic device that requires minimal user input for rapid detection of SARS-CoV-2 antibodies (ABs) in total blood and antigens associated with blood types. Here, we present a passive pressure-driven pumping technique that rapidly mixes blood samples with reagents, delivering results within three minutes. The device requires 15 mL of capillary blood and can detect SARS-CoV-2 ABs across a concentration range of 0 to 60 mg mL−1. Additionally, we demonstrated the versatility of the microfluidic device by implementing blood typing functionality, highlighting its potential for broader serological testing applications. We also developed a support vector machine (SVM) algorithm as a proof-of-concept to demonstrate the potential application of machine learning (ML)-based analysis to complement visual interpretation of results. We evaluated the performance and predictive accuracy of the SVM model and compared it to human interpretations. The analysis showed that the SVM model achieved a statistically significant improvement in predicting varying degrees of agglutination when compared to human interpretation. This device addresses the need for a user-friendly, rapid COVID-19 AB testing solution and blood-typing assay and also provides a model for the future development of diagnostic devices that are integrated with ML models for improved diagnostic accuracy and accessibility in both clinical and non-clinical environments.

A figure of the hemagglutination assay is displayed and the full article can be found at https://doi.org/10.1039/D5RA05719A.

On-chip hemagglutination assay.

 

Congratulations to Students That Have Recently Defended

Congratulations to the following students from the Gale Group who have successfully defended and/or graduated within the past year!

 Yunhao Peng

  • Dissertation Defense Date: 12/02/2024

Greg Liddiard

  • Dissertation Defense Date: 04/15/2025

Afroza Tabassum Akhi

  • Masters Graduation Date: 05/01/2025

Shamima Juthi

  • Dissertation Defense Date: 05/07/2025

Sabin Nepal

  • Dissertation Defense Date: 08/29/2025

Matt Nelson

  • Dissertation Defense Date: 10/13/2025

Publication on an Open Source Platform to Automate the Design, Validation, and Manufacture of Microfluidics

Software flow of OpenMFDA.

Brady Goenner et al. recently published “An open source platform to automate the design, verification, and manufacture of 3D printed microfluidic devices” in Scientific Reports.

Several barriers to widespread microfluidic adoption exist, including high initial fabrication costs and the labor-intensive development process. To address these barriers, a toolchain for the design, verification, and manufacturing of 3D printed microfluidic devices is presented. This work builds on existing electronic design automation (EDA) tools, yielding a toolchain that automatically lays out a microfluidic device from a library of components, simulates the device, and produces a 3D CAD file for manufacture via 3D printing. The process is validated by automatically designing and fabricating a calcium quantification assay. The full article can be found at https://doi.org/10.1038/s41598-025-15976-9.