Tri-layered composite plug for the repair of osteochondral defects: in vivo study in sheep

Author:

Yucekul Altug1,Ozdil Deniz23,Kutlu Nuri Hunkar2,Erdemli Esra4,Aydin Halil Murat5,Doral Mahmut Nedim1

Affiliation:

1. Department of Orthopedics and Traumatology, Faculty of Medicine, Hacettepe University, Ankara, Turkey

2. BMT Calsis Health Technologies Co., Ankara, Turkey

3. Bioengineering Division, Institute of Science and Engineering, Hacettepe University, Ankara, Turkey

4. Department of Histology and Embryology, School of Medicine, Ankara University, Ankara, Turkey

5. Environmental Engineering Department & Bioengineering Division and Centre for Bioengineering, Hacettepe University, Ankara, Turkey

Abstract

Cartilage defects are a source of pain, immobility, and reduced quality of life for patients who have acquired these defects through injury, wear, or disease. The avascular nature of cartilage tissue adds to the complexity of cartilage tissue repair or regeneration efforts. The known limitations of using autografts, allografts, or xenografts further add to this complexity. Autologous chondrocyte implantation or matrix-assisted chondrocyte implantation techniques attempt to introduce cultured cartilage cells to defect areas in the patient, but clinical success with these are impeded by the avascularity of cartilage tissue. Biodegradable, synthetic scaffolds capable of supporting local cells and overcoming the issue of poor vascularization would bypass the issues of current cartilage treatment options. In this study, we propose a biodegradable, tri-layered (poly(glycolic acid) mesh/poly(l-lactic acid)-colorant tidemark layer/collagen Type I and ceramic microparticle-coated poly(l-lactic acid)-poly(ϵ-caprolactone) monolith) osteochondral plug indicated for the repair of cartilage defects. The porous plug allows the continual transport of bone marrow constituents from the subchondral layer to the cartilage defect site for a more effective repair of the area. Assessment of the in vivo performance of the implant was conducted in an ovine model (n = 13). In addition to a control group (no implant), one group received the implant alone (Group A), while another group was supplemented with hyaluronic acid (0.8 mL at 10 mg/mL solution; Group B). Analyses performed on specimens from the in vivo study revealed that the implant achieves cartilage formation within 6 months. No adverse tissue reactions or other complications were reported. Our findings indicate that the porous biocompatible implant seems to be a promising treatment option for the cartilage repair.

Funder

Scientific and Technological Research Council of Turkey

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials,Medicine (miscellaneous)

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