Creation and preclinical evaluation of a novel mussel-inspired, biomimetic, bioactive bone graft scaffold: direct comparison with Infuse bone graft using a rat model of spinal fusion.


Journal

Journal of neurosurgery. Spine
ISSN: 1547-5646
Titre abrégé: J Neurosurg Spine
Pays: United States
ID NLM: 101223545

Informations de publication

Date de publication:
01 Jul 2023
Historique:
received: 18 08 2022
accepted: 20 02 2023
medline: 3 7 2023
pubmed: 7 4 2023
entrez: 6 4 2023
Statut: epublish

Résumé

Infuse bone graft is a widely used osteoinductive adjuvant; however, the simple collagen sponge scaffold used in the implant has minimal inherent osteoinductive properties and poorly controls the delivery of the adsorbed recombinant human bone morphogenetic protein-2 (rhBMP-2). In this study, the authors sought to create a novel bone graft substitute material that overcomes the limitations of Infuse and compare the ability of this material with that of Infuse to facilitate union following spine surgery in a clinically translatable rat model of spinal fusion. The authors created a polydopamine (PDA)-infused, porous, homogeneously dispersed solid mixture of extracellular matrix and calcium phosphates (BioMim-PDA) and then compared the efficacy of this material directly with Infuse in the setting of different concentrations of rhBMP-2 using a rat model of spinal fusion. Sixty male Sprague Dawley rats were randomly assigned to each of six equal groups: 1) collagen + 0.2 µg rhBMP-2/side, 2) BioMim-PDA + 0.2 µg rhBMP-2/side, 3) collagen + 2.0 µg rhBMP-2/side, 4) BioMim-PDA + 2.0 μg rhBMP-2/side, 5) collagen + 20 µg rhBMP-2/side, and 6) BioMim-PDA + 20 µg rhBMP-2/side. All animals underwent posterolateral intertransverse process fusion at L4-5 using the assigned bone graft. Animals were euthanized 8 weeks postoperatively, and their lumbar spines were analyzed via microcomputed tomography (µCT) and histology. Spinal fusion was defined as continuous bridging bone bilaterally across the fusion site evaluated via µCT. The fusion rate was 100% in all groups except group 1 (70%) and group 4 (90%). Use of BioMim-PDA with 0.2 µg rhBMP-2 led to significantly greater results for bone volume (BV), percentage BV, and trabecular number, as well as significantly smaller trabecular separation, compared with the use of the collagen sponge with 2.0 µg rhBMP-2. The same results were observed when the use of BioMim-PDA with 2.0 µg rhBMP-2 was compared with the use of the collagen sponge with 20 µg rhBMP-2. Implantation of rhBMP-2-adsorbed BioMim-PDA scaffolds resulted in BV and bone quality superior to that afforded by treatment with rhBMP-2 concentrations 10-fold higher implanted on a conventional collagen sponge. Using BioMim-PDA (vs a collagen sponge) for rhBMP-2 delivery could significantly lower the amount of rhBMP-2 required for successful bone grafting clinically, improving device safety and decreasing costs.

Identifiants

pubmed: 37021767
doi: 10.3171/2023.2.SPINE22936
doi:

Substances chimiques

Transforming Growth Factor beta 0
Bone Morphogenetic Protein 2 0
Collagen 9007-34-5
Recombinant Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113-121

Auteurs

Ethan Cottrill (E)

Departments of1Neurosurgery.
3Department of Orthopaedic Surgery, Duke University Health System, Durham, North Carolina.

Zach Pennington (Z)

Departments of1Neurosurgery.
4Department of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota.

Matthew T Wolf (MT)

2Biomedical Engineering, and.
5Laboratory of Cancer Immunometabolism, Center for Cancer Research, National Cancer Institute, Frederick, Maryland.

Naomi Dirckx (N)

6Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Jeff Ehresman (J)

Departments of1Neurosurgery.
7Department of Neurosurgery, Barrow Neurological Institute, Phoenix, Arizona.

Alexander Perdomo-Pantoja (A)

Departments of1Neurosurgery.

Christian Rajkovic (C)

Departments of1Neurosurgery.

Jessica Lin (J)

Departments of1Neurosurgery.

David R Maestas (DR)

2Biomedical Engineering, and.

Ashlie Mageau (A)

2Biomedical Engineering, and.

Dennis Lambrechts (D)

2Biomedical Engineering, and.

Veronica Stewart (V)

Departments of8Chemistry and.
9Materials Science and Engineering, Johns Hopkins University, Baltimore, Maryland; and.

Daniel M Sciubba (DM)

Departments of1Neurosurgery.
10Department of Neurosurgery, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell Health, Hempstead, New York.

Nicholas Theodore (N)

Departments of1Neurosurgery.

Jennifer H Elisseeff (JH)

2Biomedical Engineering, and.

Timothy Witham (T)

Departments of1Neurosurgery.

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Classifications MeSH