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Updated: Mar 14, 2026

Core/shell Printing Scaffolds For Tissue Engineering Of Tubular Structures
Published on: September 27, 2019
A versatile method for combining different biopolymers in a core/shell fashion by 3D plotting to achieve mechanically
Ashwini Rahul Akkineni1, Tilman Ahlfeld, Anja Lode
1Centre for Translational Bone, Joint and Soft Tissue Research, University Hospital Carl Gustav Carus and Faculty of Medicine of Technische Universität Dresden, Dresden, Germany.
This study presents a novel core/shell 3D bioprinting method using alginate shells and soft hydrogel cores. This technique creates mechanically stable scaffolds for cell integration and controlled growth factor release.
Area of Science:
- Biomaterials Engineering
- Tissue Engineering
- Bioprinting Technologies
Background:
- Three-dimensional (3D) extrusion of multiple biomaterials in a core/shell (c/s) configuration is an emerging technique for fabricating advanced constructs.
- Soft biopolymer hydrogels often lack the mechanical integrity for direct 3D plotting of open-porous structures without external support.
Purpose of the Study:
- To develop and characterize mechanically stable 3D scaffolds using a c/s extrusion approach with alginate shells and various soft hydrogel cores.
- To evaluate the potential of these scaffolds for controlled growth factor delivery and cell encapsulation in bioprinting applications.
Main Methods:
- Fabrication of c/s 3D scaffolds by extruding high-concentration alginate (shell) and low-concentration biopolymer hydrogels (core: alginate, chitosan, gellan gum, gelatin, collagen).
- Characterization of scaffold morphology, mechanical properties, and swelling behavior.
- Loading of scaffolds with growth factors (VEGF, BMP-2) and assessment of release kinetics.
- Integration of live human endothelial cells into the core material.
Main Results:
- The combination of alginate shells and soft hydrogel cores resulted in mechanically stable and robust 3D scaffolds.
- Scaffolds supported the loading and controlled release of growth factors, influenced by core composition and shell thickness.
- The fabrication process and CaCl2 crosslinking did not denature proteins within the hydrogels.
- Dual growth factor release (VEGF and BMP-2) was achieved by loading different factors into the core and shell.
- Live endothelial cells remained viable and were successfully integrated into the core material.
Conclusions:
- The developed c/s 3D bioprinting strategy enables the creation of robust scaffolds from otherwise mechanically weak hydrogels.
- This method offers tunable control over growth factor release profiles and is suitable for incorporating living cells, paving the way for advanced bioprinting applications.
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