4.7 Article

3D bioprinting of tyramine modified hydrogels under visible light for osteochondral interface

期刊

BIOFABRICATION
卷 15, 期 3, 页码 -

出版社

IOP Publishing Ltd
DOI: 10.1088/1758-5090/acd6bf

关键词

bioprinting; osteochondral interface; tyramine; alginate; carboxymethyl cellulose; in situ crosslinking

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This study developed a new 3D bioprinting approach using a combination of different materials and in situ crosslinking to fabricate tissue interfaces between cartilage and bone. The biofabricated constructs were cultured with specific media and evaluated for cell viability, morphology, and differentiation into chondrogenic and osteogenic tissues. The results showed that mechanical and chemical cues successfully induced the differentiation of human bone marrow mesenchymal stem cells into the desired tissues.
Recent advancements in tissue engineering have demonstrated a great potential for the fabrication of three-dimensional (3D) tissue structures such as cartilage and bone. However, achieving structural integrity between different tissues and fabricating tissue interfaces are still great challenges. In this study, an in situ crosslinked hybrid, multi-material 3D bioprinting approach was used for the fabrication of hydrogel structures based on an aspiration-extrusion microcapillary method. Different cell-laden hydrogels were aspirated in the same microcapillary glass and deposited in the desired geometrical and volumetric arrangement directly from a computer model. Alginate and carboxymethyl cellulose were modified with tyramine to enhance cell bioactivity and mechanical properties of human bone marrow mesenchymal stem cells-laden bioinks. Hydrogels were prepared for extrusion by gelling in microcapillary glass utilizing an in situ crosslink approach with ruthenium (Ru) and sodium persulfate photo-initiating mechanisms under visible light. The developed bioinks were then bioprinted in precise gradient composition for cartilage-bone tissue interface using microcapillary bioprinting technique. The biofabricated constructs were co-cultured in chondrogenic/osteogenic culture media for three weeks. After cell viability and morphology evaluations of the bioprinted structures, biochemical and histological analyses, and a gene expression analysis for the bioprinted structure were carried out. Analysis of cartilage and bone formation based on cell alignment and histological evaluation indicated that mechanical cues in conjunction with chemical cues successfully induced MSC differentiation into chondrogenic and osteogenic tissues with a controlled interface.

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