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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.
Abstract:
Osteoarthritis (OA) is a rapidly growing joint disease worldwide, and its chronic and progressive form can cause damage to the cartilage and subchondral bone, resulting in physical and economic suffering for affected individuals. So far, potential therapeutic approaches, such as systematic drug administration and intraarticular injections, have been used to treat OA and regenerate osteochondral defects, but they are palliative rather than curative. Thus, hydrogels with biologics (matrix-degrading enzyme inhibitors) and small molecules (growth factors, anti-inflammatory molecules) show promising results in preclinical studies but have failed in clinical practice due to inadequate patient benefits. Recently, bioinks have gained significant attention as regenerative biomaterials in tissue engineering due to their ability to contain cells and bioactive small molecules, such as proteins, peptides, and growth factors. Bioinks are developed using various polymers with crosslinkers. The crosslinkers play a crucial role in the formation of bioinks, which can be natural or synthetic (ionic, chemical, photo, etc.). However, extensive usage of crosslinkers limits the clinical application of bioinks due to compromising the ideal properties of bioinks, such as cytocompatibility, biodegradability, and biomechanical properties. Therefore, the potential solution to this problem is utilizing the click chemistry approach. The click chemistry strategy can achieve efficient bio-inks without compromising their intrinsic and optimal characteristics, as click reactions are rapid, spontaneous, and bioorthogonal, favoring the gelation time, rate of degradation, and cell viability. A few reports have delivered thorough information on click chemistry-induced hydrogels and bioinks for bone regeneration, but they are not specific to osteochondral regeneration. This review addresses this gap by exploring the fundamental concepts, challenges, and prospects of click chemistry, specifically its distinct click reactions, in developing bioinks and 3D bioprinting scaffolds for OA treatment and osteochondral regeneration. Furthermore, it addresses regulatory and clinical hurdles tied to bioink translation, providing an integrative overview of translational bioinks and tissue engineering strategies for cartilage and osteochondral regeneration.
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.

