4.6 Article

Design and fabrication method of bi-layered fibrous scaffold for cartilage regeneration

期刊

BIOCHEMICAL ENGINEERING JOURNAL
卷 182, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.bej.2022.108413

关键词

Tissue engineering; Cartilage regeneration; Scaffold; Cryo-electrospinning; Ozone treatment; Growth factor

资金

  1. [European Social Fund] [European Regional Development Fund] [01.2.2-LMT-K-718-01-0078]
  2. Research Council of Lithuania (LMTLT)

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An advanced therapy construct for cartilage regeneration was fabricated using cryo-electrospinning and contained the chondrogenic growth factor TGF beta-3. The construct was designed to promote chondral regeneration and subchondral bone formation by incorporating regenerated cellulose and hydroxyapatite.
An advanced therapy construct for regeneration of articular cartilage is reported which was fabricated by cryo-electrospinning as 3D multi-layered poly[e]caprolactone matrix harbouring chondrogenic growth factor TGF beta-3. The layers have been designed to favour the cartilage regeneration (chondral layer) and bone tissue formation (subchondral layer) by additives of regenerated cellulose and hydroxyapatite, respectively. The overall porosity of the chondral layer was 90.7% and the subchondral layer - 94.4% with a pore diameter ranges of 50-300 mu m and 75-400 mu m respectively but maintaining a low fibre diameter of 9.3 +/- 4.1 mu m and 9.1 +/- 2.1 mu m. The hydrophilicity was enhanced and functional groups essential for growth factor incorporation were introduced by surface ozone treatment. The scaffold was characterised by SEM, mu CT, FTIR, WCA, XRD, TGA, and DSC techniques. The processing of scaffold by chemical modifications resulted in the increase of biodegradability of the scaffold, as indicated by the decrease of the crystallinity, thermal stability, melting peak, and hydrophobicity, but maintaining its sufficient mechanical properties (Young's modulus equalled to 1.8 +/- 0.1 MPa for chondral layer and 1.1 +/- 0.2 MPa for subchondral). The release kinetics of TGF beta-3 followed the Korsmeyer-Peppas model, reaching 39.3% after 72 h, and the estimated 50% release after 155 h.

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