@article {19920, title = {In Vivo Performance of Hierarchical HRP-Crosslinked Silk Fibroin/β-TCP Scaffolds for Osteochondral Tissue Regeneration}, journal = {Regenerative Medicine Frontiers}, year = {2019}, month = {2019-09-18 00:00:00}, publisher = {Hapres}, abstract = {

Background: Osteochondral defects (OCD) can affect the articular cartilage and subchondral bone tissues, which requires superior therapies for the simultaneous and full restoration of such structurally and biologically different tissues.

Methods: Tissue engineered OC grafts were prepared using a horseradish peroxidase (HRP) approach to crosslink silk fibroin (HRP-SF) as the articular cartilage-like layer and an underlying HRP-SF/ZnSrTCP subchondral bone-like layer (HRP-SF/dTCP), through salt-leaching/freeze-drying methodologies. In vivo OC regeneration was assessed by implantating the hierarchical scaffolds in rabbit critical size OC defects, during 8 weeks. A comparative analysis was performed using hierarchical OC grafts made of pure β-TCP (HRP-SF/TCP).

Results: The hierarchical scaffolds showed good integration into the host tissue and no signs of acute inflammatory reaction, after 8 weeks of implantation. The histological analyses revealed positive collagen type II and glycosaminoglycans{\textquoteright} formation in the articular cartilage-like layer. New bone ingrowth{\textquoteright}s and blood vessels infiltration were detected in the subchondral bone-like layers.

Conclusions: The proposed hierarchical scaffolds presented an adequate in vivo response with cartilage tissue regeneration and calcified tissue formation specially promoted by the ionic incorporation into the subchondral bone layer, confirming the hierarchical structures as suitable for OCD regeneration.

}, keywords = {hierarchical scaffolds, Horseradish peroxidase-mediated crosslinking, Osteochondral regeneration, rabbit critical defect, Silk Fibroin, ZnSr-tricalcium phosphate}, issn = {2633-0806}, doi = {10.20900/rmf20190007}, author = {Ribeiro, V. P. and Pina, S. and Canadas, R. F. and Morais, A. and Vilela, C. and Vieira, S. and Cengiz, I. F. and Reis, R. L. and Oliveira, J. M.} }