Reconstruction of goat tibial defects using an injectable tricalcium phosphate/chitosan in combination with autologous platelet-rich plasma

被引:135
作者
Bi, Long [1 ]
Cheng, Wenjun [1 ]
Fan, Hongbin [1 ]
Pei, Guoxian [1 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Inst Orthopaed & Traumatol, Xian 710032, Peoples R China
关键词
Platelet-rich plasma; Tricalcium phosphate; Chitosan; Bone regeneration; LONG-BONE DEFECTS; CELLS IN-VITRO; GROWTH-FACTOR; OSTEOBLASTS; SCAFFOLDS; DIFFERENTIATION; PROLIFERATION; REGENERATION; DELIVERY; MATRICES;
D O I
10.1016/j.biomaterials.2010.01.038
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Injectable scaffolds held great promise for the reconstruction of bone defects. We prepared an injectable composite named PTC by combining TCP/chitosan (TC) with platelet-rich plasma (PRP). The objective of this study was to investigate the composite's mechanical and biological properties. First, we found that the introduction of PRP in TC showed no adverse effect on mechanical strength and that there were no significant differences in compressive strength between PTC and TC (P > 0.05). In cell culture experiments, both cell count and alkaline phosphatase (ALP) activity measurements of PTC were higher than those of TC. The high levels of Cbfa1 and TGF-beta were detected early in PTC-induced MSCs by reverse transcriptase polymerase chain reaction. Bone formation following expression of collagen type I. osteocalcin, osteonectin and calcium nodules was also observed in PRP-induced MSCs. Finally, this composite was injected into the tibial bone defect in a goat model, and its ability to induce bone regeneration was observed. Sixteen weeks after the implantation of this composite, the tibial defects had completely recuperated, with significantly better formation of mature bone and less residual material than in the control. These results demonstrate that our composite, with its concomitant mechanical strength, biocompatibility, and osteoinductive properties, has significant potential as an injectable material for the treatment of bone defects. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3201 / 3211
页数:11
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