A Multi‐Crosslinkable Methacrylated Alginate‐GelMa Bioink for Drop‐on‐Demand Bioprinting

ABSTRACT To advance biofabrication, this work presents the development of a multi‐crosslinkable bioink based on methacrylated alginate di‐aldehyde (ADAMa) combined with gelatine methacryloyl (GelMa). ADAMa was synthesized using methacrylic anhydride under specific conditions, and successful functionalization as well as changes in chain length were confirmed by NMR (Nuclear Magnetic Resonance), ATR‐FTIR (Attenuated Total Reflectance—Fourier Transform Infrared Spectroscopy), and GPC (Gel Permeation Chromatography) analyses. The resulting ADAMa–GelMa bioink can be crosslinked via several independent mechanisms, including UV‐initiated photopolymerization, enzymatic crosslinking, Schiff‐base formation, and ionic gelation with calcium ions. Our study confirms an increase in the compressive modulus with increasing GelMa content, ranging from 0.3 to 30 kPa, and in vitro biocompatibility for ADAMa–GelMa bioink with enhanced cell–material interaction for a 25:75 ADAMa–GelMa ratio. Furthermore, Drop‐on‐Demand (DoD) bioprinting performance was evaluated using filament fusion test and grid structure test analyses, along with structural fidelity assessment of free‐standing pillar arrays, including metrics such as pillar height and spacing. Multiphoton microscopy further revealed homogeneous cell distribution within printed pillars. Overall, this system provides tuneable mechanical properties, high cell viability, and strong structural fidelity, making it a promising candidate for the fabrication of complex, cell‐laden constructs in advanced biofabrication applications.

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Publication Details

Journal
Macromolecular Bioscience
Published
2026-10-31
DOI
https://doi.org/10.1002/mabi.70278
Primary Topic
3D Printing in Biomedical Research
Type
article
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article

A Multi‐Crosslinkable Methacrylated Alginate‐GelMa Bioink for Drop‐on‐Demand Bioprinting

Julian Bauer, Jessica Faber, Jörg Teßmar, Aldo Roberto Boccaccini et al.
Macromolecular Bioscience
3D Printing in Biomedical Research
article

A Multi‐Crosslinkable Methacrylated Alginate‐GelMa Bioink for Drop‐on‐Demand Bioprinting

Julian Bauer, Jessica Faber, Jörg Teßmar, Aldo Roberto Boccaccini, Oliver Friedrich, Rainer Detsch, Silvia Budday, Emine Karakaya, Jonas Röder, Tommi Bui
article en

Abstract

ABSTRACT To advance biofabrication, this work presents the development of a multi‐crosslinkable bioink based on methacrylated alginate di‐aldehyde (ADAMa) combined with gelatine methacryloyl (GelMa). ADAMa was synthesized using methacrylic anhydride under specific conditions, and successful functionalization as well as changes in chain length were confirmed by NMR (Nuclear Magnetic Resonance), ATR‐FTIR (Attenuated Total Reflectance—Fourier Transform Infrared Spectroscopy), and GPC (Gel Permeation Chromatography) analyses. The resulting ADAMa–GelMa bioink can be crosslinked via several independent mechanisms, including UV‐initiated photopolymerization, enzymatic crosslinking, Schiff‐base formation, and ionic gelation with calcium ions. Our study confirms an increase in the compressive modulus with increasing GelMa content, ranging from 0.3 to 30 kPa, and in vitro biocompatibility for ADAMa–GelMa bioink with enhanced cell–material interaction for a 25:75 ADAMa–GelMa ratio. Furthermore, Drop‐on‐Demand (DoD) bioprinting performance was evaluated using filament fusion test and grid structure test analyses, along with structural fidelity assessment of free‐standing pillar arrays, including metrics such as pillar height and spacing. Multiphoton microscopy further revealed homogeneous cell distribution within printed pillars. Overall, this system provides tuneable mechanical properties, high cell viability, and strong structural fidelity, making it a promising candidate for the fabrication of complex, cell‐laden constructs in advanced biofabrication applications.

Macromolecular BioscienceVol. 26(11)
Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), University of Würzburg (DE)
Openalex Percentile: Top 24%
3D Printing in Biomedical Research
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