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首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Continuous delivery of rhBMP2 and rhVEGF165 at a certain ratio enhances bone formation in mandibular defects over the delivery of rhBMP2 alone - An experimental study in rats
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Continuous delivery of rhBMP2 and rhVEGF165 at a certain ratio enhances bone formation in mandibular defects over the delivery of rhBMP2 alone - An experimental study in rats

机译:与单独递送rhBMP2相比,以一定比例连续递送rhBMP2和rhVEGF165可以增强下颌骨缺损的骨形成-大鼠的实验研究

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The aim of the present study was to test the hypothesis that different amounts of vascular endothelial growth factor and bone morphogenic protein differentially affect bone formation when applied for repair of non-healing defects in the rat mandible. Porous composite PDLLA/CaCO3 carriers were fabricated as slow release carriers and loaded with rhBMP2 and rhVEGF(165) in 10 different dosage combinations using gas foaming with supercritical carbon dioxide. They were implanted in non-healing defects of the mandibles of 132 adult Wistar rats with additional lateral augmentation. Bone formation was assessed both radiographically (bone volume) and by histomorphometry (bone density). The use of carriers with a ratio of delivery of VEGF/BMP between 0.7 and 1.2 was significantly related to the occurrence of significant increases in radiographic bone volume and/or histologic bone density compared to the use of carriers with a ratio of delivery of <= 0.5 when all intervals and all outcome parameters were considered. Moreover, simultaneous delivery at this ratio helped to "save" rhBMP2 as both bone volume and bone density after 13 weeks were reached/surpassed using half the dosage required for rhBMP2 alone. It is concluded, that the combined delivery of rhVEGF(165) and rhBMP2 for repair of critical size mandibular defects can significantly enhance volume and density of bone formation over delivery of rhBMP2 alone. It appears from the present results that continuous simultaneous delivery of rhVEGF(165) and rhBMP2 at a ratio of approximately 1 is favourable for the enhancement of bone formation. (C) 2015 Published by Elsevier B.V.
机译:本研究的目的是检验以下假设:当修复大鼠下颌骨的非愈合缺损时,不同量的血管内皮生长因子和骨形态发生蛋白会不同地影响骨形成。将多孔复合PDLLA / CaCO3载体制成缓释载体,并使用超临界二氧化碳进行气体发泡,以10种不同剂量组合装载rhBMP2和rhVEGF(165)。将它们植入了132只成年Wistar大鼠下颌骨的非愈合缺损中,并进行了额外的侧向增强。通过射线照相术(骨体积)和组织形态测定法(骨密度)评估骨形成。与使用VEGF / BMP输送比在0.7到1.2之间的载体相比,与使用射线照相骨量和/或组织学骨密度显着增加的发生相比,与使用输送比<=当考虑所有间隔和所有结果参数时为0.5。此外,以该比例同时递送有助于“保存” rhBMP2,因为仅使用rhBMP2所需剂量的一半即可达到/超过13周后的骨体积和骨密度。结论是,与单独递送rhBMP2相比,联合递送rhVEGF(165)和rhBMP2修复临界大小的下颌骨缺损可显着增强骨形成的体积和密度。从目前的结果看来,以约1的比率连续同时递送rhVEGF(165)和rhBMP2有利于增强骨形成。 (C)2015由Elsevier B.V.发布

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