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Related Experiment Video

Updated: Oct 27, 2025

Bioprinting Cellularized Constructs Using a Tissue-specific Hydrogel Bioink
08:34

Bioprinting Cellularized Constructs Using a Tissue-specific Hydrogel Bioink

Published on: April 21, 2016

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From Thermogelling Hydrogels toward Functional Bioinks: Controlled Modification and Cytocompatible Crosslinking.

Lukas Hahn1, Matthias Beudert2, Marcus Gutmann2

  • 1Functional Polymer Materials, Chair for Advanced Materials Synthesis, Institute for Functional Materials and Biofabrication, Department of Chemistry and Pharmacy and Bavarian Polymer Institute, Julius-Maximilians-University Würzburg, Röntgenring 11, Würzburg, 97070, Germany.

Macromolecular Bioscience
|July 22, 2021
PubMed
Summary

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In Vitro Biofilm Formation on 3D-Printed, Milled, and Conventionally Manufactured Denture Base Resins.

Bioengineering (Basel, Switzerland)·2026

This study introduces a novel bioink using Diels-Alder chemistry for stable, printable hydrogels. The resulting materials demonstrate excellent shape fidelity and biocompatibility for cell encapsulation in biofabrication.

Area of Science:

  • Biomaterials Science
  • Polymer Chemistry
  • Tissue Engineering

Background:

  • Hydrogels are crucial for biofabrication, providing printability and stability.
  • Diels-Alder chemistry offers a versatile platform for hydrogel modification.

Purpose of the Study:

  • To develop a novel bioink system based on thermogelling diblock copolymers.
  • To utilize Diels-Alder click chemistry for enhanced hydrogel stability and cell integration.

Main Methods:

  • Diblock copolymers of poly(2-methyl-2-oxazoline) and poly(2-n-propyl-2-oxazine) were synthesized and modified.
  • Post-polymerization modification involved hydrolysis and coupling with furan and maleimide moieties.
  • RGD-peptides were incorporated using thiol-maleimide chemistry for cell adhesion.
Keywords:
biofabricationbioprintingchemical crosslinkinghydrogels

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Main Results:

  • The modified diblock copolymers exhibited excellent printability due to thermogelling and shear-thinning properties.
  • Trigger-less Diels-Alder click chemistry ensured long-term shape fidelity.
  • Functionalization with RGD-peptides promoted fibroblast adhesion, proliferation, and good cytocompatibility in encapsulated cells.

Conclusions:

  • A versatile two-step bioink system combining physical gelation and chemical crosslinking was established.
  • The platform allows for easy incorporation of bioactive moieties for enhanced cellular interaction and biomechanical properties.
  • The developed bioink demonstrates high potential for advanced biofabrication applications.