4.2 Article

Effects of Recombinant Human Bone Morphogenetic Protein-2 Dose and Ceramic Composition on New Bone Formation and Space Maintenance in a Canine Mandibular Ridge Saddle Defect Model

Journal

TISSUE ENGINEERING PART A
Volume 22, Issue 5-6, Pages 469-479

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/ten.tea.2015.0355

Keywords

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Funding

  1. National Science Foundation [0847711]
  2. Army
  3. Navy
  4. NIH
  5. Air Force
  6. VA
  7. Health Affairs [W81XWH-14-2-0004]
  8. U.S. Army Medical Research Acquisition Activity, Chandler Street, Fort Detrick, MD
  9. Department of Education for a Graduate Assistance in Areas of National Need Fellowship [P200A090323]
  10. NIH [S10RR027631]
  11. Direct For Mathematical & Physical Scien
  12. Division Of Materials Research [0847711] Funding Source: National Science Foundation

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Treatment of mandibular osseous defects is a significant clinical challenge. Maintenance of the height and width of the mandibular ridge is essential for placement of dental implants and restoration of normal dentition. While guided bone regeneration using protective membranes is an effective strategy for maintaining the anatomic contour of the ridge and promoting new bone formation, complications have been reported, including wound failure, seroma, and graft exposure leading to infection. In this study, we investigated injectable low-viscosity (LV) polyurethane/ceramic composites augmented with 100 mu g/mL (low) or 400 mu g/mL (high) recombinant human bone morphogenetic protein-2 (rhBMP-2) as space-maintaining bone grafts in a canine mandibular ridge saddle defect model. LV grafts were injected as a reactive paste that set in 5-10 min to form a solid porous composite with bulk modulus exceeding 1 MPa. We hypothesized that compression-resistant LV grafts would enhance new bone formation and maintain the anatomic contour of the mandibular ridge without the use of protective membranes. At the rhBMP-2 dose recommended for the absorbable collagen sponge carrier in dogs (400 mu g/mL), LV grafts maintained the width and height of the host mandibular ridge and supported new bone formation, while at suboptimal (100 mu g/mL) doses, the anatomic contour of the ridge was not maintained. These findings indicate that compression-resistant bone grafts with bulk moduli exceeding 1 MPa and rhBMP-2 doses comparable to that recommended for the collagen sponge carrier support new bone formation and maintain ridge height and width in mandibular ridge defects without protective membranes.

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