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Composite Alginate Dialdehyde-Gelatin (ADA-GEL) Hydrogel Containing Short Ribbon-Shaped Fillers for Skeletal Muscle
Lys Sprenger1, Hsuan-Heng Lu2, Steffen Trippmacher3
1Department of Biomaterials, Faculty of Engineering Science, University of Bayreuth, Prof.-Rüdiger-Bormann Str. 1, 95447 Bayreuth, Germany.
ACS Applied Materials & Interfaces
|August 19, 2024
Summary
This study developed a novel composite bioink using oxidized alginate and gelatin with cell-laden fillers to improve skeletal muscle tissue regeneration. Optimized plasma treatment and cross-linking conditions enhanced cell adhesion, alignment, and viability for reconstructive applications.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Regenerative Medicine
Background:
- Skeletal muscle damage often exceeds self-repair capabilities, requiring advanced biofabrication and tissue engineering solutions.
- Developing anisotropic structures with enhanced cell alignment is crucial for effective skeletal muscle tissue reconstruction.
Purpose of the Study:
- To create a composite bioink from oxidized alginate (ADA) and gelatin (GEL) with cell-laden fillers for skeletal muscle tissue engineering.
- To optimize plasma treatment and protein coating for poly(lactic-co-glycolic acid) (PLGA) ribbon surfaces to improve cell adhesion.
- To determine the optimal calcium chloride (CaCl2) concentration for cross-linking ADA-GEL hydrogels, evaluating physical, mechanical, and cellular properties.
Main Methods:
- Fabrication of a composite bioink using oxidized alginate (ADA) and gelatin (GEL) with ribbon-shaped fillers.
- Evaluation of different plasma treatments and fibronectin coating on PLGA ribbon surfaces for cell adhesion.
- Investigation of various CaCl2 concentrations for ionic cross-linking of ADA-GEL hydrogels.
- Assessment of hydrogel properties including pore size, degradation, mechanical strength, cell viability, and proliferation.
Main Results:
- Oxygen plasma activation (30 W, 5 min) followed by fibronectin coating significantly enhanced cell adhesion and differentiation on PLGA ribbons.
- The optimal cross-linking concentration for the ADA-GEL formulation (2.5%w/v ADA, 3.75%w/v GEL) was determined to be 60 mM CaCl2.
- The optimized hydrogels exhibited a compression modulus similar to native muscle tissue (11.5 kPa), high C2C12 cell viability (>80%), and robust proliferation over 7 days.
- Rheological analysis confirmed the composite bioink's suitability, demonstrating shear-thinning and favorable flow behavior.
Conclusions:
- A composite bioink of oxidized alginate and gelatin with functionalized fillers shows significant promise for skeletal muscle tissue engineering.
- Optimized surface treatment and cross-linking strategies are critical for enhancing cell integration and mechanical properties of engineered muscle constructs.
- This bioink formulation supports high cell viability and proliferation, offering a viable platform for future muscle regenerative therapies.

