ArticlePolymers2025
Engineering Poly(L-Lactic Acid)/Hydroxyapatite Scaffolds via Melt-Electrowriting: Enhancement of Osteochondral Cell Response in Human Nasal Chondrocytes.
Article in Polymers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
1 citing paper in PubMed.
- Melt Electrowritten Scaffold-Reinforced Affibody-Conjugated Hydrogels for Controlled Bone Morphogenetic Protein-2 Delivery.bioRxiv : the preprint server for biology · 2025Article
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Authors and funding
13 authors.
Funding
Abstract
Osteochondral repair remains challenging due to cartilage's limited self-healing capacity and the structural complexity of the osteochondral interface, particularly the hypertrophic layer anchoring cartilage to bone. We fabricated melt electrowritten (MEW) poly(L-lactic acid) (PLLA) scaffolds incorporating 1%, 5%, and 10% hydroxyapatite (HAp) to provide a precise fiber architecture (~200 μm pores) and bone-mimetic biochemical cues. Human nasal chondrocytes (hNCs), currently in clinical trials for knee cartilage repair, were selected for their phenotypic plasticity and established safety profile, facilitating translational potential. HAp-PLLA scaffolds, especially at higher HAp contents, enhanced hNC adhesion, proliferation, mineralization, and maintenance of cartilage-specific ECM compared to PLLA alone. This work demonstrates the first high-HAp MEW-printed PLLA scaffold for osteochondral repair, integrating architectural precision with bioactivity in a clinically relevant cell-material system.
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Registered trials
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