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1.
Arch Oral Biol ; 60(5): 724-9, 2015 May.
Article in English | MEDLINE | ID: mdl-25748392

ABSTRACT

OBJECTIVE: Although it has been shown that rifamycin is an effective agent for bone graft decontamination, no information exists on the effects of rifamycin decontamination on bone graft incorporation. The aim of this study was to evaluate the influence of rifamycin decontamination on the incorporation of autologous onlay bone grafts quantitatively. DESIGN: In 30 rats, a standardized 5.0-mm-diameter bone graft was harvested from the right mandibular angle, contaminated with saliva, decontaminated with rifamycin solution, and augmented to the left as an onlay graft. Ten animals were sacrificed at 7, 14, and 21 days after surgery. In the control group (10 rats), the onlay grafts were neither contaminated nor decontaminated, and the rats were sacrificed at 21 days after surgery. Histological slides were prepared from each grafted site for both immunohistochemistry analysis (bone morphogenetic protein-2 (BMP-2) and vascular endothelial growth factor (VEGF) antibodies) and histometric analysis. Images obtained from the graft incorporation area with the light microscope were transferred to a PC, and they were evaluated using Clemex PE 3.5 image analysis software. RESULTS: The grafts were fully incorporated in all specimens. The results showed that rifamycin decontamination has no detrimental effect on graft incorporation and the findings revealed a tendency for earlier revascularization and osteogenesis in the decontamination group. Data were analyzed using variance analysis and Tukey's test. CONCLUSIONS: Rifamycin decontamination has no detrimental effect on autogenous graft incorporation, and it can be used for graft decontamination with confidence.


Subject(s)
Bone Transplantation , Decontamination/methods , Mandible/transplantation , Rifamycins/pharmacology , Animals , Bone Morphogenetic Protein 2/metabolism , Immunohistochemistry , Rats , Rats, Wistar , Transplantation, Autologous , Vascular Endothelial Growth Factor A/metabolism , Wound Healing/drug effects
2.
ScientificWorldJournal ; 2013: 396091, 2013.
Article in English | MEDLINE | ID: mdl-23935417

ABSTRACT

INTRODUCTION: The aim of this study was to analyze the effects of screw design and force application on the stability of miniscrews, using RTT, SEM, and histomorphometric analyses. MATERIALS AND METHODS: Eighty cylindrical, self-drilling, and Ti6Al4V alloy miniscrews (1,6 × 6 mm) were used. Four mini-screws were inserted in fibulas of each rabbit, and 115 G of force was immediately applied. Four miniscrews were inserted in the other fibula, on which no force was applied. Eight weeks after insertion, osseointegration between miniscrew and the surrounding bone was evaluated by the histomorphometric analyses, SEM, and RTT. Kruskal-Wallis and the paired t-tests were used for statistical analysis. RESULTS: Values obtained from Group I were significantly higher than those of the other loaded groups (P < .05). There were no differences in RTT scores among Groups II, III, and IV. Similar findings were also observed for unloaded mini-screws. There was no significant difference between Groups I and I(C), while the differences between loaded and unloaded controls for each miniscrew were statistically significant. CONCLUSIONS: Immediate loading of miniscrews does not impair screw stability. Also, the diameter of miniscrew and more frequent thread pitches have a positive effect on stability; however, length of miniscrews does not have a significant effect on the stability.


Subject(s)
Bone Screws , Dentistry , Animals , Rabbits , Surface Properties
3.
Int J Oral Maxillofac Surg ; 40(12): 1395-400, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21945486

ABSTRACT

This study compared the effect of systemic and local administration of alendronate on distraction osteogenesis in rabbit mandibles. Thirty New Zealand white rabbits were allocated to 3 groups: 10 rabbits for systemic alendronate; 9 for local alendronate; and 11 as controls. After a 5 day latency period, distraction was performed at a rate of 0.8mm/day for 9 days via a custom-made distractor. Animals were killed at the end of the consolidation period of 28 days. The distracted mandibles were harvested and evaluated by plain radiography, computed tomography (CT), dual energy X-ray absorptiometry (DEXA), and histomorphometry. Histologically, comparing the systemic and local alendronate groups, there were no statistically significant differences in the bone healing parameters, but each group showed a statistically superior effect over the control group (p<0.05). Quantitative CT evaluation showed a significant difference mean in the density of the regeneration between experimental and control groups. There was a significant increase in mean bone mineral density in the experimental groups compared with the control group. Histologic, CT, and DEXA analysis demonstrated that using systemic and local alendronate may be effective in accelerating new bone formation in the distraction gap in rabbit mandibles.


Subject(s)
Alendronate/administration & dosage , Bone Density Conservation Agents/administration & dosage , Mandible/drug effects , Osteogenesis, Distraction/methods , Absorptiometry, Photon/methods , Administration, Oral , Administration, Topical , Animals , Bone Density/drug effects , Bone Regeneration/drug effects , Drug Carriers , Gelatin Sponge, Absorbable/administration & dosage , Image Processing, Computer-Assisted/methods , Male , Mandible/pathology , Mandible/surgery , Osteogenesis/drug effects , Osteogenesis, Distraction/instrumentation , Rabbits , Tablets , Tomography, X-Ray Computed/methods
4.
J Oral Maxillofac Surg ; 66(5): 905-10, 2008 May.
Article in English | MEDLINE | ID: mdl-18423279

ABSTRACT

PURPOSE: To assess the effect of systemic administration of zoledronic acid (ZA) on mineralization of newly formed bone and to determine strain-related osteoporosis on surrounding bone during lengthening of immature rabbit mandible. MATERIALS AND METHODS: Eighteen New Zealand white rabbits were divided randomly into 2 groups, and bone lengthening was carried out in the left portion of the mandible through distraction osteogenesis with a rate of 0.5 mm every 12 hours for 5 days. The experimental group was administered 0.1 mg/kg ZA intravenously. The control group was given saline infusion only during operation. All animals were sacrificed at the end of the 28-day consolidation period. The mandibles of all animals were removed and regenerate was evaluated. Osteoblasts, osteoclasts, collagen fibers, and fibroblasts were marked within 0.1-mm(2) area and newly formed bone area was measured within 0.5-mm(2) area. All data were analyzed using Mann-Whitney U test. RESULTS: Although irregular bone destruction spots were seen in the control group, the experimental group showed regular ossification areas and significant difference between osteoblast and osteoclast numbers (P < .05). In the regenerate zone, there was considerable difference between the 2 groups in terms of osteoblast, osteoclast, and collagen amounts (P < .05). Additionally, newly formed bone areas and fibroblast count were higher in experimental group. CONCLUSIONS: The results of this study showed that ZA had positive effects on the new bone formation, which may potentially shorten the consolidation period.


Subject(s)
Bone Density Conservation Agents/pharmacology , Bone Regeneration/drug effects , Diphosphonates/pharmacology , Imidazoles/pharmacology , Mandibular Advancement/methods , Osteogenesis, Distraction , Animals , Calcification, Physiologic/drug effects , Cell Proliferation/drug effects , Collagen/biosynthesis , Dental Stress Analysis , Fibroblasts/drug effects , Male , Mandible/surgery , Mandibular Advancement/adverse effects , Osteoblasts/drug effects , Osteoclasts/drug effects , Osteogenesis, Distraction/adverse effects , Osteoporosis/etiology , Osteoporosis/prevention & control , Rabbits , Random Allocation , Zoledronic Acid
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