Abstract

Self-assembling bioinks offer the possibility to biofabricate with molecular precision, hierarchical control, and biofunctionality. For this to become a reality with widespread impact, it is essential to engineer these ink systems ensuring reproducibility and providing suitable standardization. We have reported a self-assembling bioink based on disorder-to-order transitions of an elastin-like recombinamer (ELR) to co-assemble with graphene oxide (GO). Here, we establish reproducible processes, optimize printing parameters for its use as a bioink, describe new advantages that the self-assembling bioink can provide, and demonstrate how to fabricate novel structures with physiological relevance. We fabricate capillary-like structures with resolutions down to ∼10 µm in diameter and ∼2 µm thick tube walls and use both experimental and finite element analysis to characterize the printing conditions, underlying interfacial diffusion-reaction mechanism of assembly, printing fidelity, and material porosity and permeability. We demonstrate the capacity to modulate the pore size and tune the permeability of the resulting structures with and without human umbilical vascular endothelial cells. Finally, the potential of the ELR-GO bioink to enable supramolecular fabrication of biomimetic structures was demonstrated by printing tubes exhibiting walls with progressively different structure and permeability.

Highlights

  • Bioinks are increasingly playing a leading role in the quest for recreating the structures and functions of biological systems [1]

  • Taking advantages of these opportunities, we have recently reported on a multicomponent self-assembly mechanism harnessing disorder-to-order transitions of an elastin-like recombinamer (ELR) to non-covalently co-assemble with graphene oxide (GO) [29]

  • We study in more detail the diffusion-reaction process to better control the ELK1-GO co-assembly, formation of the tubular structure, and the properties of the interfacial membrane including thickness, porosity, and permeability

Read more

Summary

April 2021

Attribution 4.0 licence. 6 CREATE LAB, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London.

Introduction
Methods
2.10. Cell culture
Results and discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.