Source abstract
Abstract
Abstract All‐liquid molding can be used to transform a liquid into free‐form solid constructs, while maintaining internal fluidity. Traditional biological scaffolds, such as cured pre‐gels, are normally processed in solid state, sacrificing flowability and permeability. However, it is essential to maintain the fluidity of the scaffold to truly mimic the complexity and heterogeneity of natural human tissues. Here, this work molds an aqueous biomaterial ink into liquid building blocks with rigid shapes while preserving internal fluidity. The molded ink blocks for bone‐like vertebrae and cartilaginous‐intervertebral‐disc shapes, are magnetically manipulated to assemble into hierarchical structures as a scaffold for subsequent spinal column tissue growth. It is also possible to join separate ink blocks by interfacial coalescence, different from bridging solid blocks by interfacial fixation. Generally, aqueous biomaterial inks are molded into shapes with high fidelity by the interfacial jamming of alginate surfactants. The molded liquid blocks can be reconfigured using induced magnetic dipoles, that dictated the magnetic assembly behavior of liquid blocks. The implanted spinal column tissue exhibits a biocompatibility based on in vitro seeding and in vivo cultivating results, showing potential physiological function such as bending of the spinal column.
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Research context
OpenAlex topics: 3D Printing in Biomedical Research · Pickering emulsions and particle stabilization · Hydrogels: synthesis, properties, applications
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Affiliations
Department of Plastic Surgery Union Hospital Tongji Medical College Huazhong University of Science and Technology Wuhan 430022 China
CAS Key Laboratory of Bio‐Inspired Materials and Interfacial Science Technical Institute of Physics and Chemistry Chinese Academy of Sciences Beijing 100190 China
Materials Sciences Division Lawrence Berkeley National Laboratory Berkeley California 94720 USA
Beijing Advanced Innovation Center for Soft Matter Science and Engineering Beijing University of Chemical Technology Beijing 100029 P. R. China
Polymer Science and Engineering Department University of Massachusetts Amherst Massachusetts 01003 USA
Funding
China Postdoctoral Science Foundation · National Natural Science Foundation of China
References (29)
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