Advanced Science· 2026Q1
Liquid‐Responsive Shape‐Memory Nanofiber‐Reinforced Scaffolds for Cartilage Repair
- 0citations
- Q1SCImago
- 2026year
Short summary
A novel scaffold (QCG-2%F/KGN) uses liquid-responsive, shape-memory nanofibers within a porous matrix to conformally fill cartilage defects and promote endogenous regeneration by sustained release of chondrogenic factors.
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Key points
- Developed a liquid-responsive, shape-memory, core-shell nanofiber-reinforced scaffold (QCG-2%F/KGN) for cartilage repair.
- The scaffold's aligned microchannels and rough nanofiber network promote cell infiltration, stability, and water retention.
- Sustained release of KGN from core-shell fibers over 30 days stimulated chondrogenic differentiation and matrix deposition in vitro.
- In a rat model, the scaffold conformally filled defects and enhanced hyaline cartilage-like regeneration, indicated by specific gene markers (SOX9, COL2A1, ACAN) and reduced inflammation.
AI-generated from the title and abstract; the full text is not read.
Abstract
ABSTRACT Bioengineered scaffolds hold promise for articular cartilage repair but are often limited by poor defect conformity, insufficient availability of endogenous reparative cells, and inadequate chondrogenic stimulation. Here, we developed a liquid‐responsive shape‐memory, core–shell nanofiber‐reinforced, directionally porous scaffold (QCG‐2%F/KGN) for endogenous cartilage regeneration. KGN‐loaded SF/PCL–PVA core–shell nanofibers were fabricated by coaxial electrospinning, fragmented, incorporated into a quaternized chitosan/gelatin matrix, and assembled by directional freeze‐casting. The aligned microchannels provided a structurally permissive route for cell infiltration and distribution, while the nanofiber network enhanced pore‐wall roughness, structural stability, water retention, and hydration‐triggered shape recovery. The core–shell fibers also enabled sustained KGN release over 30‐day period. In vitro, QCG‐2%F/KGN maintained high cell viability and promoted BMSC migratory activity, spreading, chondrogenic differentiation, and cartilage‐matrix deposition. In a rat full‐thickness cartilage‐defect model, the scaffold conformally filled the defect and enhanced hyaline cartilage like regeneration, accompanied by increased SOX9, COL2A1, and ACAN and decreased COL1A1 and MMP13. Transcriptomic analysis further indicated enrichment of cartilage‐anabolic programs and attenuation of inflammatory signaling. These findings support a sequential regenerative strategy integrating shape‐adaptive implantation, a microarchitecture favorable for endogenous cell infiltration, and sustained chondrogenic induction.
The authors' abstract, as published at the source. Advanced Science, 2026 · DOI ↗
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Field: Rheumatology
RheumatologyMedicine