Long‐term pre‐clinical evaluation of an injectable chitosan nanocellulose hydrogel with encapsulated adipose‐derived stem cells in an ovine model for IVD regeneration

ORCID
0000-0003-0861-0578
Affiliation
Halle Wittenberg, Department for Orthopaedics and Traumatology Martin Luther University Halle (Saale) Germany
Schmitt, Christine;
Affiliation
Halle Wittenberg, Department for Orthopaedics and Traumatology Martin Luther University Halle (Saale) Germany
Radetzki, Florian;
Affiliation
Department of Biological and Macromolecular Materials Fraunhofer Institute for Microstructure of Materials and Systems IMWS Halle (Saale) Germany
Stirnweiss, Annika;
GND
1057905496
Affiliation
Department of Trauma, Hand and Reconstructive Surgery Universitätsklinikum Jena Jena Germany
Mendel, Thomas;
Affiliation
Department of Biomedical Engineering University of Florida Gainesville Florida USA
Ludtka, Christopher;
Affiliation
Translational Centre for Regenerative Medicine University of Leipzig Leipzig Germany
Friedmann, Andrea;
Affiliation
Translational Centre for Regenerative Medicine University of Leipzig Leipzig Germany
Baerthel, Andre;
Affiliation
Department of Veterinary Medicine University of Leipzig Leipzig Germany
Brehm, Walther;
Affiliation
Spinplant GmbH Halle Germany
Milosevic, Javorina;
Affiliation
Spinplant GmbH Halle Germany
Meisel, Hans Jörg;
Affiliation
Translational Centre for Regenerative Medicine University of Leipzig Leipzig Germany
Goehre, Felix;
Affiliation
Translational Centre for Regenerative Medicine University of Leipzig Leipzig Germany
Schwan, Stefan

The potential therapeutic benefit of adipose‐derived stem cells (ASCs) encapsulated in an injectable hydrogel for stimulating intervertebral disc (IVD) regeneration has been assessed by a number of translational and preclinical studies. However, previous work has been primarily limited to small animal models and short‐term outcomes of only a few weeks. Long‐term studies in representative large animal models are crucial for translation into clinical success, especially for permanent stabilization of major defects such as disc herniation. An injectable chitosan carboxymethyl cellulose hydrogel scaffold loaded with ASCs was evaluated regarding its intraoperative handling, crosslinking kinetics, cell viability, fully‐crosslinked viscoelasticity, and long‐term therapeutic effects in an ovine model. Three IVDs per animal were damaged in 10 sheep. Subcutaneous adipose tissue was the source for autologous ASCs. Six weeks after IVD damage, two of the damaged IVDs were treated via ASC‐loaded hydrogel injection. After 12 months following the implantation, IVD disc height and histological and cellular changes were assessed. This system was reliable and easy to handle intraoperatively. Over 12 months, IVD height was stabilized and degeneration progression significantly mitigated compared to untreated, damaged IVDs. Here we show for the first time in a large animal model that an injectable chitosan carboxymethyl cellulose hydrogel system with encapsulated ASCs is able to affect long‐term stabilization of an injured IVD and significantly decrease degeneration processes as compared to controls.

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