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Updated: Mar 21, 2026

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Microfluidic Bioprinting for Engineering Vascularized Tissues and Organoids
Published on: August 11, 2017
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A toolbox for microvalve-based bioprinting
Irem Deniz Deniz Derman1,2, Medine Dogan Sarikaya1,2,3, Yasar Ozer Yilmaz1,2,4
1Engineering Science and Mechanics Department, Penn State University, University Park, PA 16802, United States of America.
Biofabrication
|March 19, 2026
Summary
This study introduces a quantitative printability toolbox for microvalve-based bioprinting (MBB) bioinks. It establishes viscosity and concentration thresholds for reproducible tissue biofabrication.
Area of Science:
- Biomaterials Science
- Biotechnology
- Tissue Engineering
Background:
- Microvalve-based bioprinting (MBB) is crucial for precise biofabrication.
- Standardized methods for assessing bioink printability in MBB are limited.
- Bioink properties significantly impact droplet formation and tissue structure.
Purpose of the Study:
- To develop a quantitative printability toolbox for evaluating bioinks in MBB.
- To systematically analyze the influence of rheological properties and contact angle on bioink printability.
- To provide a framework for bioink optimization in MBB for reproducible biomedical applications.
Main Methods:
- Evaluation of bioinks (fibrinogen, collagen type I, Matrigel, alginate) using a quantitative printability toolbox.
- Systematic analysis of rheological properties and contact angle effects on ligament formation and droplet ejection.
- High-speed imaging to capture ligament dynamics and droplet-substrate interactions.
- Investigation of Tween 20 (T20) surfactant for improved droplet uniformity.
Main Results:
- Identification of specific viscosity and concentration thresholds for each bioink.
- Development of a comprehensive printability map correlating bioink properties with ligament stability and droplet printability.
- Demonstration that rheological properties and contact angle are key determinants of MBB printability.
- Tween 20 (T20) was shown to reduce interfacial aggregation and enhance droplet uniformity.
Conclusions:
- The developed printability toolbox enables quantitative assessment of bioinks for MBB.
- The established printability map guides bioink selection and optimization for reproducible tissue biofabrication.
- This framework facilitates the advancement of MBB for creating complex biological structures in biomedical applications.

