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Updated: Jan 19, 2026

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Creating Transient Cell Membrane Pores Using a Standard Inkjet Printer
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Engineering inkjet bioprinting processes toward translational therapies
Ioannis Angelopoulos1, Mark C Allenby2, Mayasari Lim3
1Department of Biomedical Research, Foundation of Research and Technology-Hellas, Institute of Molecular Biology and Biotechnology, Ioannina, Greece.
Biotechnology and Bioengineering
|September 24, 2019
Summary
Inkjet-based 3D bioprinting uses cell-laden biomaterials to create tissue constructs for regenerative medicine. Overcoming challenges in bioink development and manufacturing is crucial for clinical translation.
Area of Science:
- Biomedical Engineering
- Materials Science
- Regenerative Medicine
Background:
- 3D bioprinting constructs tissues using cell-laden biomaterials via additive manufacturing.
- Inkjet printing offers high resolution for bioprinting, crucial for tissue engineering.
- Clinical translation of bioprinting faces significant process engineering challenges.
Purpose of the Study:
- To review recent advances in inkjet-based 3D bioprinting.
- To emphasize available biomaterials, their properties, and construct generation for medical applications.
- To address current challenges and future directions for bioprinting and bioinks, focusing on mass production and regulatory aspects.
Main Methods:
- Review of recent advancements in inkjet-based 3D bioprinting technologies.
- Analysis of biomaterials used in bioprinting, including their properties and synthesis.
- Examination of upstream (bioink formulation) and downstream (sterilization, culture, implantation) challenges.
Main Results:
- Recent progress in bioink development and inkjet bioprinting techniques.
- Identification of key biomaterials and their suitability for specific medical applications.
- Highlighting the critical need for scalable manufacturing and regulatory compliance.
Conclusions:
- Bioprinting holds immense potential for tissue engineering and regenerative medicine.
- Addressing challenges in bioink formulation, process engineering, and regulatory pathways is essential for clinical impact.
- Future efforts must focus on mass production and adherence to regulatory standards for successful translation.

