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Submicron Patterns-on-a-Chip: Fabrication of a Microfluidic Device Incorporating 3D Printed Surface Ornaments.
Mahdiyeh Nouri-Goushki1, Abhishek Sharma2, Luigi Sasso2
1Department of Biomechanical Engineering, Faculty of Mechanical, Maritime, and Materials Engineering, Delft University of Technology (TU Delft), Mekelweg 2, 2628 CD Delft, The Netherlands.
ACS Biomaterials Science & Engineering
|January 6, 2021
Summary
Researchers developed a microfluidic platform with 3D submicron pillars for bone regeneration research. This advanced in vitro model mimics the bone microenvironment, enabling better study of cell behavior and tissue development.
Area of Science:
- Biomaterials Engineering
- Tissue Engineering
- Microfluidics
Background:
- Studying bone regeneration requires in vitro models that replicate the complex, multiscale architecture of bone tissue.
- Existing methods face challenges in creating high-fidelity, large-area submicron topographies for 3D cell cultures.
Purpose of the Study:
- To engineer a microfluidic platform with reproducible, large-area submicron pillar topographies for advanced bone regeneration research.
- To demonstrate the capability of two-photon polymerization for fabricating multiscale structures within a microfluidic device.
Main Methods:
- Utilized two-photon polymerization (2PP) with optimized parameters and direct laser writing to create uniform submicron pillar patterns.
- Integrated submicron pillars of varying heights onto 3D microscaffolds in a single fabrication step.
- Assessed surface hydrophilicity, mechanical stability under flow, and cytotoxicity of the fabricated materials.
Main Results:
- Successfully fabricated a microfluidic platform with mm-scale, reproducible submicron pillar topographies.
- Demonstrated multiscale fabrication by integrating pillars of different heights onto 3D microscaffolds.
- Observed improved surface hydrophilicity and stability at flow rates up to 8 mL/min.
- Confirmed no cytotoxic effects of the IP-Dip resin on human mesenchymal stromal cells in dynamic culture.
Conclusions:
- This study presents a significant advancement in creating submicron structure-on-a-chip models for bone regeneration.
- The developed microfluidic platform offers a promising tool for high-throughput in vitro studies of bone tissue engineering.
- The fabrication method allows for precise control over microscale features essential for mimicking the native tissue microenvironment.

