Multi-layered collagen-based scaffolds for osteochondral defect repair in rabbits

• Published in: Acta biomaterialia 2016-03, Vol.32, p.149-160
• Main Authors: Levingstone, Tanya J., Thompson, Emmet, Matsiko, Amos, Schepens, Alexander, Gleeson, John P., O’Brien, Fergal J.
• Format: Article
• Language: English
• Subjects: Animals; Biocompatibility; Biomedical materials; Bones; Cartilage; Cattle; Collagen; Collagen - pharmacology; Defects; Female; Femur - diagnostic imaging; Femur - drug effects; Femur - pathology; Femur - surgery; Immunohistochemistry; In vivo; Multilayers; Osteochondral; Rabbits; Repair; Scaffolds; Surgical implants; Sus scrofa; Tissue engineering; Tissue Scaffolds - chemistry; Wound Healing - drug effects; X-Ray Microtomography
• ISSN: 1742-7061; 1878-7568
• DOI: 10.1016/j.actbio.2015.12.034

[Display omitted] Identification of a suitable treatment for osteochondral repair presents a major challenge due to existing limitations and an urgent clinical need remains for an off-the-shelf, low cost, one-step approach. A biomimetic approach, where the biomaterial itself encourages cellular infiltration from the underlying bone marrow and provides physical and chemical cues to direct these cells to regenerate the damaged tissue, provides a potential solution. To meet this need, a multi-layer collagen-based osteochondral defect repair scaffold has been developed in our group. The objective of this study was to assess the in vivo response to this scaffold and determine its ability to direct regenerative responses in each layer in order to repair osteochondral tissue in a critical-sized defect in a rabbit knee. Multi-layer scaffolds, consisting of a bone layer composed of type I collagen (bovine source) and hydroxyapatite (HA), an intermediate layer composed of type I and type II collagen and HA; and a superficial layer composed of type I and type II collagen (porcine source) and hyaluronic acid (HyA), were implanted into critical size (3×5mm) osteochondral defects created in the medial femoral condyle of the knee joint of New Zealand white rabbits and compared to an empty control group. Repair was assessed macroscopically, histologically and using micro-CT analysis at 12weeks post implantation. Analysis of repair tissue demonstrated an enhanced macroscopic appearance in the multi-layer scaffold group compared to the empty group. In addition, diffuse host cellular infiltration in the scaffold group resulted in tissue regeneration with a zonal organisation, with repair of the subchondral bone, formation of an overlying cartilaginous layer and evidence of an intermediate tidemark. These results demonstrate the potential of this biomimetic multi-layered scaffold to support and guide the host reparative response in the treatment of osteochondral defects. Osteochondral defects, involving cartilage and the underlying subchondral bone, frequently occur in young active patients due to disease or injury. While some treatment options are available, success is limited and patients often eventually require joint replacement. To address this clinical need, a multi-layer collagen-based osteochondral defect repair scaffold designed to direct host-stem cell mediated tissue formation within each region, has been developed in our group. The present study investigates the i