Clokie Cameron M L, Moghadam Hassan, Jackson Michael T, Sandor George K B
Department of Oral and Maxillofacial Surgery, University of Toronto, 124 Edward Street, Toronto, Ontario, Canada M5B 1G6.
J Craniofac Surg. 2002 Jan;13(1):111-21; discussion 122-3. doi: 10.1097/00001665-200201000-00026.
This study evaluates bone regeneration of critical sized cranial vault defects in New Zealand white rabbits using four commercially available bone substitutes: OsteoSet (calcium sulphate pellets), DynaGraft Putty (demineralized bone matrix delivered in a poloxmer excipient), Norian CRS, and Bone Source (two commercially available calcium phosphate cements).
Critical sized defects 15 mm in diameter were created bilaterally in the parietal bones of 30 adult male New Zealand White rabbits. They were divided into three groups with ten animals in each. Bone healing was assessed clinically, radiographically, and histomorphometrically. Group 1 had calcium sulfate bioimplant on one side of the calvarium and an unfilled defect on the contralateral side. Group 2 had DBM putty on one side and Poloxamer gel on the contralateral side. Group 3, the Calcium phosphate cements (CPC), had Norian CRS on one side and Bone Source on the contralateral side. Five animals in each group were killed at 6 weeks and 12 weeks post operatively.
All unfilled defects healed with fibrous scar, as did the Plaster of Paris and the poloxamer gel defects. Defects reconstructed with the demineralized bone matrix putty healed with bone throughout the entire defect. This was obvious clinically and radiographically where the defects appeared completely filled with a dense radiopaque tissue. The six-week group displayed new bone formation (87.1%) surrounding the remaining allogeneic particles. Resorption was evidenced by the presence of osteoclastic activity and by the significant decrease in the size of the demineralized bone particles. By 12 weeks, the demineralized bone putty bioimplant was almost completely replaced by new bone (95.5%). Both calcium phosphate cement groups (Norian CRS and Bone Source) had identical patterns of healing. They clinically were visible and firm and uniformly radiopaque with little evidence of new bone formation. Histologically the cement remained unresorbed with little new bone with in the defect at 12 weeks.
The utilization of a demineralized bone matrix putty appeared to allow for complete closure of critical sized calvarial defects in New Zealand white rabbits with viable new bone at 12 weeks.
本研究使用四种市售骨替代物评估新西兰白兔临界大小颅骨缺损的骨再生情况,这四种骨替代物分别为:OsteoSet(硫酸钙颗粒)、DynaGraft Putty(以泊洛沙姆赋形剂递送的脱矿骨基质)、Norian CRS和Bone Source(两种市售磷酸钙骨水泥)。
在30只成年雄性新西兰白兔的顶骨双侧制造直径15mm的临界大小缺损。将它们分为三组,每组10只动物。通过临床、影像学和组织形态计量学评估骨愈合情况。第1组在颅骨一侧植入硫酸钙生物植入物,对侧为未填充缺损。第2组一侧植入脱矿骨基质油灰,对侧植入泊洛沙姆凝胶。第3组为磷酸钙骨水泥(CPC)组,一侧植入Norian CRS,对侧植入Bone Source。每组5只动物在术后6周和12周处死。
所有未填充缺损均通过纤维瘢痕愈合,巴黎石膏和泊洛沙姆凝胶缺损也是如此。用脱矿骨基质油灰重建的缺损在整个缺损处均通过骨愈合。这在临床和影像学上很明显,缺损处似乎完全被致密的不透射线组织填充。六周组在剩余的同种异体颗粒周围显示出新骨形成(87.1%)。破骨细胞活性的存在以及脱矿骨颗粒大小的显著减小证明了吸收的存在。到12周时,脱矿骨油灰生物植入物几乎完全被新骨替代(95.5%)。两组磷酸钙骨水泥(Norian CRS和Bone Source)具有相同的愈合模式。它们在临床上可见且质地坚硬,均匀不透射线,几乎没有新骨形成的迹象。组织学上,12周时骨水泥仍未被吸收,缺损内几乎没有新骨。
使用脱矿骨基质油灰似乎可以使新西兰白兔临界大小的颅骨缺损在12周时通过有活力的新骨完全闭合。