The Rheology and Printability of Cartilage Matrix-Only Biomaterials

Biomolecules. 2022 Jun 17;12(6):846. doi: 10.3390/biom12060846.

Abstract

The potential chondroinductivity from cartilage matrix makes it promising for cartilage repair; however, cartilage matrix-based hydrogels developed thus far have failed to match the mechanical performance of native cartilage or be bioprinted without adding polymers for reinforcement. There is a need for cartilage matrix-based hydrogels with robust mechanical performance and paste-like precursor rheology for bioprinting/enhanced surgical placement. In the current study, our goals were to increase hydrogel stiffness and develop the paste-like precursor/printability of our methacryl-modified solubilized and devitalized cartilage (MeSDVC) hydrogels. We compared two methacryloylating reagents, methacrylic anhydride (MA) and glycidyl methacrylate (GM), and varied the molar excess (ME) of MA from 2 to 20. The MA-modified MeSDVCs had greater methacryloylation than GM-modified MeSDVC (20 ME). While GM and most of the MA hydrogel precursors exhibited paste-like rheology, the 2 ME MA and GM MeSDVCs had the best printability (i.e., shape fidelity, filament collapse). After crosslinking, the 2 ME MA MeSDVC had the highest stiffness (1.55 ± 0.23 MPa), approaching the modulus of native cartilage, and supported the viability/adhesion of seeded cells for 15 days. Overall, the MA (2 ME) improved methacryloylation, hydrogel stiffness, and printability, resulting in a stand-alone MeSDVC printable biomaterial. The MeSDVC has potential as a future bioink and has future clinical relevance for cartilage repair.

Keywords: bioprinting; cartilage; extracellular matrix; hydrogels; methacryloylation; rheology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biocompatible Materials*
  • Cartilage*
  • Hydrogels
  • Mercaptoethanol
  • Rheology
  • Tissue Engineering

Substances

  • Biocompatible Materials
  • Hydrogels
  • Mercaptoethanol

Grants and funding

This work was supported by the University of Oklahoma Office of the Vice President for Research and Partnerships Postdoc Stimulus Award (E.A.K), and the University of Oklahoma Undergraduate Research Opportunities Program (E.E.T.).