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An LCD 3D-printed microphysiological system with deflectable extracellular matrix thin films
Matt D Nelson1, Patrick A Tresco2, Amirhossein Razaghian3
1Biomedical Engineering, University of Utah, 36 S Wasatch Dr #3100, Salt Lake City, Utah, 84112, United States.
Biomedical Materials (Bristol, England)
|July 21, 2026
Summary
Researchers developed a novel 3D-printed microphysiological system (MPS) using LCD technology. This advanced MPS model supports lung epithelial cells and offers microfluidic flow and cyclic strain for better in vivo recapitulation.
Area of Science:
- Biotechnology
- Biomedical Engineering
- Tissue Engineering
Background:
- Microphysiological systems (MPS) offer improved in vivo microenvironment recapitulation.
- Current MPS manufacturing methods often limit scalability and complex 3D architectures.
Purpose of the Study:
- To develop a scalable and versatile 3D-printed microphysiological system (MPS).
- To incorporate microfluidic flow, cyclic strain, and a permeable extracellular matrix (ECM) substrate.
Main Methods:
- Utilized Liquid Crystal Display (LCD) 3D printing for fabrication.
- Integrated microfluidic channels and a thin, permeable ECM substrate (~5 µm dehydrated, ~70 kDa permeability).
- Sustained NCI-H441 lung epithelial cells on the substrate for over one week.
Main Results:
- Successfully fabricated an MPS with microfluidic flow and cyclic strain capabilities.
- Demonstrated the substrate's permeability and ability to support lung epithelial cell viability for extended periods.
- Confirmed resistance to rhodamine absorption, indicating material stability.
Conclusions:
- LCD 3D printing provides a scalable strategy for advanced MPS fabrication.
- The developed MPS platform can be adapted for various organ systems.
- This approach enables the creation of MPS with intricate designs for enhanced biological research.

