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Versatile Compartmentalization of Hydrogel-Medium Interfaces in Microfluidic Channels for Reconstructing Complex
Byengkyu Kang1, Yong Hun Jung1, Ju-Hee Kim2
1School of Mechanical Engineering, Korea University, Seoul02841, Republic of Korea.
ACS Applied Materials & Interfaces
|August 13, 2026
Summary
This study introduces a novel weir-based microfluidic platform for precise hydrogel patterning in complex tissue models. The platform enables stable, continuous compartmentalization for advanced tissue engineering applications.
Area of Science:
- Biomaterials Engineering
- Microfluidics
- Tissue Engineering
Background:
- Replicating complex in vivo tissue geometries in vitro is challenging.
- Current micropillar-based microfluidic methods create segmented interfaces, limiting continuous compartment design.
Purpose of the Study:
- To develop a weir-based microfluidic platform for continuous hydrogel patterning in complex, tissue-relevant architectures.
- To establish a predictive design framework for stable hydrogel compartmentalization.
Main Methods:
- Development of a weir-based microfluidic platform.
- Theoretical analysis and computational simulations to predict hydrogel front advancement and interface failure.
- Experimental validation of the design framework and platform capabilities.
- Engineering of complex 3D vascular networks and renal epithelial tubes.
Main Results:
- The weir-based platform enables stable hydrogel patterning across diverse and complex geometries.
- A pressure-based design framework accurately predicts hydrogel filling stability.
- Identified critical intersection geometries prone to failure and provided layout guidelines.
- Successfully engineered interconnected 3D vascular networks and continuous renal epithelial tubes.
Conclusions:
- The developed platform significantly improves the predictability and design versatility of microfluidic hydrogel compartmentalization.
- This approach facilitates the creation of more physiologically relevant tissue models with complex, continuous architectures.
- Enables the study of how local connectivity and spatial architecture influence tissue morphogenesis.

