Short Communication - (2025) Volume 15, Issue 1
Received: 01-Mar-2025, Manuscript No. bda-25-169233;
Editor assigned: 03-Mar-2025, Pre QC No. P-169233;
Reviewed: 17-Mar-2025, QC No. Q-169233;
Revised: 22-Mar-2025, Manuscript No. R-169233;
Published:
31-Mar-2025
, DOI: 10.37421/2090-5025.2025.15.294
Citation: Rinaldi, Greta. "Functional Bioceramics in Osteochondral Repair and Cartilage Tissue Engineering." Bioceram Dev Appl 15 (2025): 294.
Copyright: © 2025 Rinaldi G. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
The development of bilayered or gradient bioceramic scaffolds that mimic the natural transition from cartilage to bone has been a major advancement in this field. These scaffolds are engineered to possess a cartilage-like layer with high porosity and a bone-like layer with greater stiffness and mineral content, thereby replicating the hierarchical structure of native osteochondral units. Materials such as Hydroxyl Apatite (HA), Tri Calcium Phosphate (TCP) and bioactive glass are often used for the subchondral bone region, while composite or polymer-ceramic blends are employed to support chondrogenesis in the upper layer. This stratified design enables region-specific cellular responses, encouraging chondrocyte proliferation in the cartilage zone and osteoblast differentiation in the bone zone, ultimately fostering simultaneous regeneration.
In addition to structural design, functionalization of bioceramic scaffolds has further enhanced their therapeutic effectiveness. Incorporating growth factors such as Transforming Growth Factor-Beta (TGF-β), Bone Morphogenetic Proteins (BMPs) and Vascular Endothelial Growth Factor (VEGF) into the scaffold matrix promotes cellular signaling pathways crucial for tissue development. Moreover, nanostructuring of surfaces and doping with elements like magnesium, zinc, or strontium enhances the osteoinductive and chondroinductive properties of the ceramics. Controlled release systems embedded within the bioceramics allow for localized, time-sensitive delivery of these biomolecules, thus improving cell recruitment and matrix synthesis at the defect site.
Recent research also emphasizes the integration of bioceramic scaffolds with stem cell-based therapies to boost regenerative outcomes. Mesenchymal Stem Cells (MSCs), when seeded onto these scaffolds, exhibit improved adhesion, proliferation and lineage-specific differentiation, particularly when the surface chemistry and topography are optimized. Bioceramics can also be used as carriers in bioprinting applications, enabling the fabrication of patient-specific constructs with tailored mechanical and biological profiles. Together, these innovations position functional bioceramics as a cornerstone technology in restoring osteochondral integrity and promoting long-term joint functionality [2].
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