Bioorthogonal Click Chemistry Engineered Bioinks for 3D Bioprinting in Osteochondral Regeneration and Osteoarthritis

Chithra Anilkumar1,2, Anjaneyulu Udduttula1,3

  • 1Centre for Biomaterials, Cellular and Molecular Theranostics (CBCMT), Vellore Institute of Technology (VIT), Vellore 632014, Tamil Nadu, India.

Insights

Click chemistry offers a promising solution for developing advanced bioinks for osteoarthritis (OA) treatment. This approach enhances bioink properties for effective osteochondral regeneration, overcoming limitations of current therapies.

Area of Science:

  • Biomaterials Science
  • Regenerative Medicine
  • Tissue Engineering

Background:

  • Osteoarthritis (OA) is a progressive joint disease causing cartilage and bone damage, with current treatments offering only palliative relief.
  • Existing hydrogel therapies for OA and osteochondral defects have shown limited clinical success due to issues with biologics and small molecules.
  • Bioinks are emerging as crucial biomaterials for tissue engineering, but traditional crosslinking methods compromise essential properties like cytocompatibility and biodegradability.

Purpose of the Study:

  • To review the application of click chemistry in developing advanced bioinks for osteoarthritis (OA) and osteochondral regeneration.
  • To explore the fundamental concepts, challenges, and prospects of distinct click reactions in creating bioinks and 3D bioprinting scaffolds for OA treatment.
  • To provide an integrative overview of translational bioinks and tissue engineering strategies for cartilage and osteochondral regeneration, addressing regulatory and clinical hurdles.

Main Methods:

  • Review of existing literature on click chemistry, bioinks, and osteochondral regeneration.
  • Analysis of distinct click reactions and their advantages in bioink formulation.
  • Exploration of 3D bioprinting strategies utilizing click chemistry-based bioinks for cartilage and bone repair.

Main Results:

  • Click chemistry enables the development of bioinks with improved gelation, degradation rates, and cell viability.
  • This approach overcomes limitations associated with traditional crosslinkers, enhancing cytocompatibility and biomechanical properties.
  • Click chemistry-based bioinks show significant potential for osteochondral regeneration, addressing a gap in current regenerative strategies.

Conclusions:

  • Click chemistry presents a powerful strategy for creating advanced bioinks tailored for osteochondral regeneration in OA treatment.
  • Addressing regulatory and clinical challenges is crucial for the successful translation of these bioinks into clinical practice.
  • This review highlights the potential of click chemistry to advance tissue engineering solutions for cartilage and osteochondral defects.

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