Ulvan structural modification enhances stability and cell compatibility of GelMa based bioinks for tissue engineering
- Manlin Li 1, Ying Zhou 2, Xifang Chen 2, Zhilian Yue 2, Pia Winberg 3, Gordon G Wallace 2
- Manlin Li 1, Ying Zhou 2, Xifang Chen 2
- 1College of Chemistry and Pharmacy, Northwest A&F University, Yangling, Shaanxi 712100, PR China.
- 2Intelligent Polymer Research Institute, Faculty of Engineering and Information Sciences, Innovation Campus, University of Wollongong, Wollongong, NSW 2522, Australia.
- 3Venus Shell System, 220 Bolong Rd, Bomaderry, NSW 2541, Australia.
- 0College of Chemistry and Pharmacy, Northwest A&F University, Yangling, Shaanxi 712100, PR China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study introduces modified ulvan (UAMa) for improved 3D biofabrication with gelatin methacryloyl (GelMa). UAMa enhances bio-ink stability and hydrogel strength, showing promise for tissue engineering scaffolds.
Area Of Science
- Biomaterials Science
- Tissue Engineering
- Polymer Chemistry
Background
- Ulvan and gelatin methacryloyl (GelMa) are promising bio-inks for 3D printing.
- Previous formulations faced solution stability issues, impacting storage and printing.
- Structural modification of ulvan is needed to overcome these limitations.
Purpose Of The Study
- To develop a structurally modified ulvan (UAMa) for enhanced GelMa-based bio-inks.
- To improve solution stability and mechanical properties of ulvan-GelMa composites.
- To evaluate the potential of UAMa-based hydrogels for tissue engineering applications.
Main Methods
- Ulvan purification via deproteinization.
- Chemical modification of purified ulvan with adipic dihydrazide and methacryloyl chloride to create UAMa.
- Formulation of UAMa-GelMa bio-inks and preparation of UAMa-based hydrogels (UAMaG) as controls.
- 3D printing of scaffolds and assessment of solution stability, mechanical strength, and cytocompatibility.
Main Results
- The UAMa-GelMa ink solution exhibited enhanced stability compared to controls.
- UAMa-based hydrogels (UAMaG) showed superior mechanical strength over methacrylated ulvan-based hydrogels (UMaG).
- 3D printed scaffolds demonstrated high cytocompatibility with primary human dermal fibroblasts.
Conclusions
- The hydrazine groups in modified ulvan (UAMa) significantly contribute to improved hydrogel performance.
- UAMa-GelMa composites offer enhanced solution stability and mechanical properties for advanced biofabrication.
- UAMa-based structures show considerable potential for tissue engineering applications.
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