Gale Students Attend BMES

On October 21st-24th, two Gale Group students attended the Biomedical Engineering Society (BMES) 2026 Annual Meeting in Orlando, FL. Camden Long had a podium presentation and Jade Bookwalter presented a poster. The conference was a great opportunity to connect with others in the department and network with other biomedical engineers across different universities and institutions.

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Gale Group Attends MicroTAS 2026

The 30th International Conference on Miniaturized Systems for Chemistry and Life Sciences took place from October 18th-22nd in Granada, Spain. Dr. Bruce Gale presented Munawar Jawad’s work and Erica Francis and Forest Siewert presented their work via poster presentations during the conference. At MicroTAS, insights were gained and connections made, especially related to our project on microfluidic design automation. Check out our automation efforts and begin your own custom design at https://openmfda.org/.

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Gale Students Present Research at UBEC 2026

The 21st annual Utah Biomedical Engineering Conference (UBEC) took place on October 2nd at The University of Utah. Three students from the Gale Group participated in the conference. Munawar Jawad and Jade Bookwalter had podium presentations, and Camden Long had a poster presentation. UBEC was a great opportunity to exchange ideas with others in the field and communicate our latest research.

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Publication on an LCD 3D-Printed Microphysiological System

Matt D Nelson et al. recently authored “An LCD 3D-printed microphysiological system with deflectable extracellular matrix thin films” that was accepted for publication in Biomedical Materials. The article can be found at https://doi.org/10.1088/1748-605X/ae8e15.

Abstract: Microphysiological systems (MPS) have emerged as promising models to better recapitulate in vivo microenvironments, but they often rely on manufacturing techniques that limit their scalability and constrain non-trivial three-dimensional architectures. Here, LCD 3D printing was used to fabricate an MPS capable of microfluidic flow, physiologically relevant cyclic strain, and resistance to rhodamine absorption. The device contains a thin, permeable (readily up to ~70 kDa) extracellular matrix (ECM) substrate ( ~5 µm dehydrated) that can sustain NCI-H441 lung epithelial cells for a period of at least one week. This microfabrication strategy may be extended to different organ systems, enabling researchers to fabricate MPS with more complex designs.

Fatemeh Momeni Receives Poster Award at iSFFF Meeting

Fatemeh Momeni recently received the Best Poster Award at the iSFFF Conference in Washington, DC. Fatemeh’s poster highlighted her research on the retention behavior of different PFAS compounds in cyclical electrical field-flow fractionation.

Congratulations, Fatemeh!

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Publication on Key Operating Parameters on the Retention and Separation of Ions

Mark Shad et al. published “Effect of Key Operating Parameters on the Retention and Separation of Ions Using Cyclical Electrical Field Flow Fractionation” in Analytical Chemistry. The full article can be found at https://doi.org/10.1021/acs.analchem.5c03277.

Graphical abstract.

Abstract: The analysis of inorganic ions is critical in the environmental, industrial, and medical fields, with ion chromatography (IC) being the most used method. While IC offers high accuracy and reproducibility, its high cost, complexity, and operational constraints necessitate the development of alternative methods. This study explores the application of CyElFFF, a variant of electrical field-flow fractionation, for ion retention and separation. The CyElFFF with channel dimensions of 25 μm height, 10 cm length, and 0.5 cm width was developed, incorporating a conductivity detector and CO2 suppressor. Parameters affecting retention time and separation resolution, including injection volume, ion concentration, and electric field conditions, were evaluated. Results showed enhanced ion retention and separation resolution at lower ion concentrations and optimized electric field settings in mode III. Separation of K+, Na+, NO3–, and SO42– was demonstrated with separation resolution improved by reducing frequency and flow rate. These findings establish CyElFFF as a promising approach for ion analysis.

 

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

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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.

 

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.