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Human Cartilage Tissue Fabrication Using Three-dimensional Inkjet Printing Technology
Published on: June 10, 2014
Mucin-Based Dual Cross-Linkable IPN Hydrogel Bioink for 3D Bioprinting and Cartilage Tissue Engineering
Sruthi C Sasikumar1, Upashi Goswami1, Ashok M Raichur1,2
1Department of Materials Engineering, Indian Institute of Science Bangalore, Karnataka 560012, India.
This study developed a novel double cross-linked hydrogel bioink for cartilage tissue engineering. The new material, incorporating alginate and hyaluronic acid, shows promise for cartilage repair by mimicking native tissue properties.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Tissue Engineering
Background:
- Cartilage has limited self-repair capabilities, driving the need for advanced tissue engineering (TE) solutions.
- Developing functional scaffolds is crucial for cartilage regeneration, requiring materials that mimic native tissue properties.
- Existing bioinks often lack the necessary mechanical strength and biological cues for effective cartilage TE.
Purpose of the Study:
- To engineer a novel double cross-linked interpenetrating network (IPN) hydrogel bioink for cartilage TE.
- To incorporate alginate and hyaluronic acid (HA) into a MuMA-based bioink to enhance scaffold properties.
- To evaluate the printability, mechanical properties, degradation, and biocompatibility of the developed bioink for chondrocyte support.
Main Methods:
- Fabrication of a double cross-linked IPN hydrogel using photo-cross-linkable MuMA and ionically cross-linkable alginate.
- Addition of hyaluronic acid (HA) to the hydrogel formulation to leverage its cartilage-beneficial properties.
- Comprehensive characterization including morphology, swelling, degradation, mechanical testing, rheology, printability assessment, and in vitro biocompatibility assays using C28/I2 chondrocytes.
Main Results:
- The double cross-linked MuMA-alginate-HA hydrogels demonstrated compressive moduli comparable to native cartilage.
- Double cross-linking significantly influenced scaffold degradation, water uptake, and porosity, enhancing stability.
- Biocompatibility testing confirmed the bioink's ability to support C28/I2 cell proliferation and chondrogenic potential.
Conclusions:
- The developed double cross-linked IPN hydrogel represents a promising advancement in cartilage tissue engineering.
- The incorporation of alginate and HA into the MuMA bioink significantly improved scaffold properties for cartilage regeneration.
- This mucin-based bioink shows potential for specialized applications in cartilage repair and regeneration.
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