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Bioactive coatings on 3D printed scaffolds for bone regeneration: use of Laponite® to deliver BMP-2 in an ovine femoral condyle defect model

Abstract:
Biomaterial-based approaches for bone regeneration seek to explore alternative strategies to repair non-healing fractures and critical-sized bone defects. Fracture non-union occurs due to a number of factors resulting in the formation of bone defects. Rigorous evaluation of the biomaterials in relevant models and assessment of their potential to translate towards clinical use is vital. Large animal experimentation can be used to model fracture non-union while scaling-up materials for clinical use. Growth factors modulate cell phenotype, behaviour and initiate signalling pathways leading to changes in matrix deposition and tissue formation. Bone morphogenetic protein-2 (BMP-2) is a potent osteogenic growth factor, with a rapid clearance time in vivo necessitating clinical use at a high dose, with potential deleterious side-effects. The current studies have examined the potential for Laponite® nanoclay coated poly(caprolactone) trimethacrylate (PCL-TMA900) scaffolds to bind BMP-2 for enhanced osteoinduction in a large animal critical-sized bone defect. An ovine femoral condyle defect model confirmed PCL-TMA900 scaffolds coated with Laponite®/BMP-2 produced significant bone formation compared to the uncoated PCL-TMA 900 scaffold in vivo, assessed by micro-computed tomography (μCT) and histology. This indicated the ability of Laponite® to deliver the bioactive BMP-2 on the PCL-TMA900 scaffold. Bone formed around the Laponite®/BMP-2 coated PCL-TMA900 scaffold, with no erroneous bone formation observed away from the scaffold material confirming localisation of BMP-2 delivery. The current studies demonstrate the ability of a nanoclay to localise and deliver bioactive BMP-2 within a tailored octet-truss scaffold for efficacious bone defect repair in a large animal model with significant implications for translation to the clinic.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.bioadv.2024.213959

Authors

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Role:
Author
ORCID:
0000-0002-6809-9807
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Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy and Genetics
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy and Genetics
Role:
Author
ORCID:
0000-0002-0179-4098
More by this author
Role:
Author
ORCID:
0000-0002-9733-5477


More from this funder
Funder identifier:
https://ror.org/03x94j517
Grant:
MR/R015651/1
More from this funder
Funder identifier:
https://ror.org/001aqnf71
Grant:
EP/X027163/1
More from this funder
Funder identifier:
https://ror.org/00cwqg982
Grant:
MR/R015651/1
BB/R015651/1


Publisher:
Elsevier
Journal:
Biomaterials Advances More from this journal
Volume:
164
Article number:
213959
Place of publication:
Netherlands
Publication date:
2024-07-18
Acceptance date:
2024-07-14
DOI:
EISSN:
2772-9508
ISSN:
2772-9516
Pmid:
39083876


Language:
English
Keywords:
Pubs id:
2018002
Local pid:
pubs:2018002
Deposit date:
2025-07-04
ARK identifier:

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