Recombinant human bone morphogenetic protein-2 (rhBMP-2) was encapsulated in biodegradable poly(DL-lactide-co-glycolide) (PLGA) capsules to regenerate bone by controlling the release rate of rhBMP-2. The rhBMP-2/PLGA capsules containing 12 g of rhBMP-2 were implanted in seven 15-mm segmental defects
Closing capacity of segmental radius defects in rabbits
✍ Scribed by Esther W.H. Bodde; Paul H.M. Spauwen; Antonios G. Mikos; John A. Jansen
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 731 KB
- Volume
- 85A
- Category
- Article
- ISSN
- 1549-3296
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
In the research of synthetic bone graft substitutes, the relevance for bone regeneration can be confirmed in a critical‐sized model. In this study the rabbit radial defect was investigated as an ingenious model of critical size, due to its defect immobilizing intact ulna. In addition, the influence of poly(DL‐lactic‐co‐glycolic acid) (PLGA) on bone regeneration was determined. Sixteen, 4‐month‐old rabbits received bilateral segmental radial defects of 15 or 20 mm. The osteotomy ends were marked with small titanium pins. Half of the group received injected PLGA microparticle/carboxymethylcellulose implants. Implantation time was 12 weeks. Evaluation consisted of radiographs after surgery and sacrifice, microcomputed tomography and histology. The radiographs revealed that the created defects were significantly smaller after sacrifice. Further a number of radii showed fibrocartilaginous interposition. Both findings indicated instability of the created defect. All evaluation techniques revealed that 15 and 20 mm were not of critical size, as most defects were more or less regenerated. PLGA microparticles did not influence bone regeneration significantly. In conclusion, 15‐ and 20‐mm radius defects in 4‐month‐old rabbits were not a suitable model for bone regeneration as these defects were neither critical size nor stable. PLGA‐microparticle degradation did not influence bone regeneration. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res 2008
📜 SIMILAR VOLUMES
## Abstract If segmental nerve defects could be repaired by elongating the proximal or distal segments, nerve grafting might be unnecessary. We elongated a 40‐mm proximal segment of an injured median nerve, in the rabbit right forelimb, at a rate of 1 mm/day for 10 days in 10 rabbits and for 15 day
## Abstract Segmental nerve defects have been repaired with nerve grafts. However, regenerating fibers must go through two coaptation sites, and donor site morbidities are inevitable. We elongated the distal nerve segment using a tissue expander and reconnected the nerve. We compared these results
## Abstract Calcium phosphate (Ca‐P) cement is a well established material for bone repair. The bone biological properties of Ca‐P cement can even be further improved by creating porosity in the material. The current study aimed on the evaluation of the osteoconductive behavior of porous Ca‐P cemen
## Abstract The effects of a single local injection of recombinant human fibroblast growth factor‐2 on the healing of segmental bone defects were evaluated in rabbits. One month after the external fixator originally designed for this experiment was installed in the tibia of the rabbit, a 3‐mm bone
## Abstract The synthetic peptide, TP508 (Chrysalin®), was delivered to rabbit segmental bone defects in biodegradable controlled‐release PLGA microspheres to determine its potential efficacy for enhancing healing of non‐critically and critically sized segmental defects. Non‐critically sized radial