Fabrication of Helix aspersa Extract Loaded Gradient Scaffold with an Integrated Architecture for Osteochondral Tissue Regeneration: Morphology, Structure, and In Vitro Bioactivity.

Autor: Tamburaci S; Department of Chemical Engineering, İzmir Institute of Technology, Urla, Izmir 35430, Turkey., Perpelek M; Department of Biomechanics, Dokuz Eylul University, İzmir 35330, Turkey., Aydemir S; Department of Histology and Embryology, Dokuz Eylul University, İzmir 35330, Turkey., Baykara B; Department of Histology and Embryology, Dokuz Eylul University, İzmir 35330, Turkey., Havitcioglu H; Department of Biomechanics, Dokuz Eylul University, İzmir 35330, Turkey.; Department of Orthopedics and Traumatology, Dokuz Eylul University, İzmir 35330, Turkey., Tihminlioglu F; Department of Chemical Engineering, İzmir Institute of Technology, Urla, Izmir 35430, Turkey.
Jazyk: angličtina
Zdroj: ACS applied bio materials [ACS Appl Bio Mater] 2023 Apr 17; Vol. 6 (4), pp. 1504-1514. Date of Electronic Publication: 2023 Apr 03.
DOI: 10.1021/acsabm.2c01050
Abstrakt: Regeneration of osteochondral tissue with its layered complex structure and limited self-repair capacity has come into prominence as an application area for biomaterial design. Thus, literature studies have aimed to design multilayered scaffolds using natural polymers to mimic its unique structure. In this study, fabricated scaffolds are composed of transition layers both chemically and morphologically to mimic the gradient structure of osteochondral tissue. The aim of this study is to produce gradient chitosan (CHI) scaffolds with bioactive snail ( Helix aspersa ) mucus (M) and slime (S) extract and investigate the structures regarding their physicochemical, mechanical, and morphological characteristics as well as in vitro cytocompatibility and bioactivity. Gradient scaffolds (CHI-M and CHI-S) were fabricated via a layer-by-layer freezing and lyophilization technique. Highly porous and continuous 3D structures were obtained and observed with SEM analysis. In addition, scaffolds were physically characterized with water uptake test, micro-CT, mechanical analysis (compression tests), and XRD analysis. In vitro bioactivity of scaffolds was investigated by co-culturing Saos-2 and SW1353 cells on each compartment of gradient scaffolds. Osteogenic activity of Saos-2 cells on extract loaded gradient scaffolds was investigated in terms of ALP secretion, osteocalcin (OC) production, and biomineralization. Chondrogenic bioactivity of SW1353 cells was investigated regarding COMP and GAG production and observed with Alcian Blue staining. Both mucus and slime incorporation in the chitosan matrix increased the osteogenic differentiation of Saos-2 and SW1353 cells in comparison to the pristine matrix. In addition, histological and immunohistological staining was performed to investigate ECM formation on gradient scaffolds. Both characterization and in vitro bioactivity results indicated that CHI-M and CHI-S scaffolds show potential for osteochondral tissue regeneration, mimicking the structure as well as enhancing physical characteristics and bioactivity.
Databáze: MEDLINE