Wang Yan, Wan Chao, Szöke George, Ryaby James T, Li Gang
Department of Orthopaedic Surgery, General Hospital of Chinese People's Liberation Army, Beijing 100853, People's Republic of China.
J Orthop Res. 2008 Apr;26(4):539-46. doi: 10.1002/jor.20495.
We have previously demonstrated that injections of the thrombin-related peptide, TP508, into the lengthening gap have significantly enhanced bone consolidation in a rabbit model of distraction osteogenesis. This study was to further test the effect of a single TP508 injection in slow release preparation on bone formation during distraction osteogenesis. Rabbits had left tibiae lengthened unilateral lengthener at rate of 1.4 mm/day for 6 days. TP508 was injected into as the following: Group 1, TP508 in saline; Group 2, in PPF/PLGA [poly(propylene fumarate)/poly(D,L-lactic-co-glycolic acid)] microparticles; and Group 3, dextran gel only. All the animals were killed 2 weeks after lengthening. On radiographies, more bone was formed in the two TP508-treated groups at first and secnd week postlengthening than that of the control Group 3. Microcomputed tomography (microCT) at 2 weeks indicated that the most advanced bone formation and remodeling was seen in Group 2. The mean volumetric BMD of the regenerates was significantly higher in the TP508 treated groups compared to the control group (p < 0.05). Histological evaluations supported the radiographic and the microCT results. In conclusion, we have demonstrated that a single injection of small amount of TP508 (300 microg) at the end of lengthening phases has significantly enhanced bone consolidation process in a rabbit model of distraction osteogenesis. The delivery of TP508 in PPF/PLGA microparticles appears to lead to a better quality bone formation over the saline delivery, further examinations are needed to confirm if PPF/PLGA microparticles may be desirable drug delivery form in augmenting bone formation.
我们之前已经证明,在牵张成骨的兔模型中,向延长间隙注射凝血酶相关肽TP508可显著增强骨愈合。本研究旨在进一步测试单次注射缓释制剂TP508对牵张成骨过程中骨形成的影响。对兔子的左胫骨使用单侧延长器以每天1.4毫米的速度延长6天。TP508按以下方式注射:第1组,TP508溶于生理盐水;第2组,TP508包封于聚富马酸丙二醇酯/聚(D,L-丙交酯-乙交酯)(PPF/PLGA)微粒中;第3组,仅注射葡聚糖凝胶。延长后2周处死所有动物。在X线片上,延长后第1周和第2周,两个TP508治疗组形成的骨比对照组第3组更多。2周时的微型计算机断层扫描(microCT)显示,第2组骨形成和重塑最明显。与对照组相比,TP508治疗组再生骨的平均体积骨密度显著更高(p<0.05)。组织学评估支持了X线和microCT结果。总之,我们已经证明,在延长阶段结束时单次注射少量TP508(300微克)可显著增强牵张成骨兔模型中的骨愈合过程。与生理盐水给药相比,PPF/PLGA微粒递送TP508似乎能导致更好质量的骨形成,是否PPF/PLGA微粒可能是促进骨形成的理想药物递送形式还需要进一步研究证实。