3D bioprinted scaffolds for osteochondral regeneration: advancements and applications
Lu J., Gao Y., Cao C., Wang H., Ruan Y., Qin K.
Narrative Review on Cartilage Damage, published in Mater Today Bio (2025) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Narrative Review
- Journal
- Mater Today Bio (2025)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 40487176
- PMCID
- PMC12145566
- DOI
- 10.1016/j.mtbio.2025.101834
- Citations
- 9
Abstract (original English)
Osteochondral defects, involving concurrent damage to articular cartilage and subchondral bone, pose significant clinical challenges due to their complex hierarchical structure and limited self-healing capacity. Traditional repair strategies often fail to replicate the biomechanical and biological gradients inherent to native osteochondral tissue, leading to suboptimal outcomes. Three-dimensional (3D) bioprinting has emerged as a transformative approach, enabling precise spatial deposition of biomaterials, cells, and signaling factors to construct biomimetic scaffolds with tailored gradients. This review systematically examines the physiological and pathological features of osteochondral units, emphasizing their zonal heterogeneity in extracellular matrix composition, mechanical properties, and cellular organization. Advancements in 3D bioprinting technologies are examined, and their efficacy in fabricating multi-layered and gradient scaffolds is evaluated. Key components of bioinks are discussed, focusing on optimizing bioink rheology, biocompatibility, and functional integration. Innovative strategies for embedding biochemical cues and designing continuous structural gradients are explored to address challenges in interfacial stress distribution and cell differentiation control. Furthermore, the design principles of biomimetic gradient scaffolds are highlighted for their crit
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is a narrative review: it collects no new patient data and does not systematically appraise evidence quality.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
How we grade evidenceBrowse all related research
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