Bioabsorbable scaffold for in situ bone regeneration

被引:13
作者
Giardino, R.
Aldini, N. Nicoli
Fini, M.
Tanzi, M. C.
Fare, S.
Draghi, L.
Carpi, A.
Nicolini, A.
Giavaresi, G.
机构
[1] Rizzoli Orthopaed Inst, Codivilla Putt Res Inst, Dept Expt Surg, I-40136 Bologna, Italy
[2] Univ Bologna, Chair Surg Pathophysiol, Bologna, Italy
[3] Politecn Milan, Dept Bioengn, Biomat Lab, I-20133 Milan, Italy
[4] Univ Pisa, Dept Reprod & Ageing, Pisa, Italy
[5] Univ Pisa, Dept Internal Med, Pisa, Italy
关键词
bone diaphyseal defects; guided bone regeneration; tissue engineering;
D O I
10.1016/j.biopha.2006.07.004
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
A non-porous poly-DL-lactide tubular chamber filled by demineralised bone matrix (DBM) and bone mar-row stromal cells (BMSC) in combination, was evaluated as a scaffold for guided bone regeneration (GBR) in an experimental model using the rabbit radius. The tubular chamber had an internal diameter of 4.7 mm, a wall thickness of 0.4 mm and a length of 18 mm. Autologous BMSC were obtained, under general anaesthesia from rabbit iliac crest and isolated by centrifugation technique. Allogenic DBM was obtained from cortico-cancellous bone of rabbits. In general anaesthesia, a 10-mm defect was bilaterally created in the radii of 10 rabbits. On the right side (experimental side) the defect was bridged with the chamber filled with both BMSC and DBM. On the left side (control side) the defect was treated by positioning DBM and BMSC between the two stumps. At an experimental time of 4 months histology and histomorphometry demonstrated that the presence of a tubular chamber significantly improved bone regrowth in the defect The mean thickness of newly-formed bone inside the chamber was about 56.7 +/- 3.74% of the normal radial cortex, in comparison with 46.7 +/- 10.7% when DBM and BMSC without the chamber were placed in the defect, P < 0.05). These results confirmed the effectiveness of the chamber as a container for factors promoting bone regeneration. (c) 2006 Elsevier SAS. All rights reserved.
引用
收藏
页码:386 / 392
页数:7
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