Combining 3D Printing and Cryostructuring to Tackle Infection and Spine Fusion

Author:

Fischetti Tiziana1ORCID,Graziani Gabriela1ORCID,Ghezzi Daniele2ORCID,Kaiser Friederike3ORCID,Hoelscher‐Doht Stefanie4,Cappelletti Martina2ORCID,Barbanti‐Bròdano Giovanni5ORCID,Groll Jürgen3ORCID,Baldini Nicola16ORCID,Gbureck Uwe3ORCID,Jungst Tomasz3ORCID

Affiliation:

1. Biomedical Science and Technologies and Nanobiotechnology Laboratory IRCCS Istituto Ortopedico Rizzoli via di Barbiano 1/10 Bologna 40136 Italy

2. Department of Pharmacy and Biotechnology University of Bologna Via Irnerio 42 Bologna 40126 Italy

3. Department for Functional Materials in Medicine and Dentistry Institute of Functional Materials and Biofabrication University of Würzburg Pleicherwall 2 D‐97070 Würzburg Germany

4. Department of Trauma, Hand, Plastic and Reconstructive Surgery University Hospital of Würzburg Oberdürrbacherstraße 6 97080 Würzburg Germany

5. Department of Spine Surgery IRCCS Istituto Ortopedico Rizzoli via di Barbiano 1/10 Bologna 40136 Italy

6. Department of Biomedical and Neuromotor Sciences Alma Mater Studiorum‐University of Bologna via Massarenti 9 Bologna 40138 Italy

Abstract

AbstractLow back pain is among the main issues in vertebral orthopaedics. Intervertebral disk degeneration can be severe, up to requiring the replacement of the damaged disk by substitutes to achieve spine fusion. Disk removal results in critical size defects, so fusion does not occur naturally, but synthetic bone grafts are needed. Since the surgical procedure is time‐consuming, high infection rates occur. Hence, in spine fusion, bone regeneration enhancement and infection prevention are needed. Here, a new dual‐component system is proposed, to tackle both issues at one time. To enable spine fusion, 3D extrusion‐based printing is employed to develop coherent custom magnesium phosphate (CaMgP)‐based cages. The 3D‐printed scaffolds are hardened, and the structural properties are evaluated to be within the ranges of physiological bone. To prevent infection, an in‐house ice‐templating device is employed in combination with a 3D‐printed ceramic scaffold, to develop tailored porous alginate structures loaded with vancomycin. Results show that CaMgP can be printed into complex geometries and that the geometry influences the pore orientation during ice‐templating. These structures loaded with vancomycin have antibacterial properties against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) strains.

Funder

H2020 European Research Council

Publisher

Wiley

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