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Fabrication of a Novel 3D Extrusion Bioink Containing Processed Human Articular Cartilage Matrix for Cartilage Tissue Engineering.
Aitchison, Alexandra Hunter; Allen, Nicholas B; Shaffrey, Isabel R; O'Neill, Conor N; Abar, Bijan; Anastasio, Albert T; Adams, Samuel B.
Afiliación
  • Aitchison AH; Department of Orthopaedic Surgery, Duke University Health System, Durham, NC 27710, USA.
  • Allen NB; Department of Orthopaedic Surgery, Duke University Health System, Durham, NC 27710, USA.
  • Shaffrey IR; Department of Orthopaedic Surgery, Duke University Health System, Durham, NC 27710, USA.
  • O'Neill CN; Department of Orthopaedic Surgery, Duke University Health System, Durham, NC 27710, USA.
  • Abar B; Department of Orthopaedic Surgery, Duke University Health System, Durham, NC 27710, USA.
  • Anastasio AT; Department of Mechanical Engineering, Duke University, Durham, NC 27710, USA.
  • Adams SB; Department of Orthopaedic Surgery, Duke University Health System, Durham, NC 27710, USA.
Bioengineering (Basel) ; 11(4)2024 Mar 28.
Article en En | MEDLINE | ID: mdl-38671751
ABSTRACT
Cartilage damage presents a significant clinical challenge due to its intrinsic avascular nature which limits self-repair. Addressing this, our study focuses on an alginate-based bioink, integrating human articular cartilage, for cartilage tissue engineering. This novel bioink was formulated by encapsulating C20A4 human articular chondrocytes in sodium alginate, polyvinyl alcohol, gum arabic, and cartilage extracellular matrix powder sourced from allograft femoral condyle shavings. Using a 3D bioprinter, constructs were biofabricated and cross-linked, followed by culture in standard medium. Evaluations were conducted on cellular viability and gene expression at various stages. Results indicated that the printed constructs maintained a porous structure conducive to cell growth. Cellular viability was 87% post printing, which decreased to 76% after seven days, and significantly recovered to 86% by day 14. There was also a notable upregulation of chondrogenic genes, COL2A1 (p = 0.008) and SOX9 (p = 0.021), suggesting an enhancement in cartilage formation. This study concludes that the innovative bioink shows promise for cartilage regeneration, demonstrating substantial viability and gene expression conducive to repair and suggesting its potential for future therapeutic applications in cartilage repair.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Bioengineering (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Bioengineering (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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