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磷酸钙复合材料构建模式对颌骨缺损修复效率的影响 被引量:3

The effectiveness of scaffolds of calcium phosphate cement composites on jaw defect repair
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摘要 目的:探讨神经多肽P物质(SP)及Ⅰ型胶原(Col-Ⅰ)复合自固化磷酸钙(CPC)构建模块化生物活性骨替代材料对其修复颌骨缺损效率的影响。方法:制备对照组单纯CPC以及试验组共价交联SP/Col-Ⅰ复合CPC、SP/Col-Ⅰ溶液混合CPC、SP溶液混合CPC再复合Col-Ⅰ海绵颗粒、SP溶液混合CPC、Col-Ⅰ溶液混合CPC材料试件,扫描电镜观察材料超微结构。将材料分别植入兔下颌骨缺损区(n=5),术后8周处死取材Micro-CT检查,观察各组材料降解及骨缺损重建情况。结果:扫描电镜检查显示Col-Ⅰ溶液混合CPC可改善材料微孔隙结构,Col-Ⅰ海绵颗粒则可于材料内部形成>300μm的大孔隙结构;术后8周Micro-CT及组织学检查示SP多肽和Col-Ⅰ均可改良CPC复合材料成骨活性,两者交联后活性显著减退;SP溶液混合CPC再复合Col-Ⅰ海绵颗粒材料诱导骨再生能力及生物降解速度显著优于其余5组材料(P<0.05)。结论:模块化设计骨替代材料利于移植应用,SP多肽、Ⅰ型胶原、CPC模块化复合材料构建模式对其生物活性有显著影响,SP释放及材料孔隙结构是决定其引导和诱导骨再生能力的关键因素。 Objective:To investigate the effectiveness of modular strategy for engineering bone scaffolds composed of synthetic neuropeptide substance P(SP),collagen type Ⅰ(Col-I) and self-setting calcium phosphate cement(CPC).Methods:6 groups of scaffolds were constructed,including CPC control,CPC mixed with SP crosslinked Col-I solution,CPC mixed with SP supplemented by Col-I solution,CPC mixed with SP solution and blended with Col-I sponge,CPC mixed with SP solution,CPC mixed with Col-I solution.The microstructure of the materials was observed by scanning electron microscope(SEM).The scaffolds were respectively implanted into rabbit mandibular bone defects(n=5).8 weeks after operation micro-CT and histological examination were performed to observe the transplants and bone defect repair.Results:SEM revealed that Col-I solution slightly improved the pore size of composite CPC.Col-I sponge created macro-pores(&gt;300 μm)inside the materials.SP and Col-I showed additive effects on the osteogenic activities of CPC scaffolds.Crosslinking SP with Col-I resulted in reduced bio-activity.The most significant bone ingrowth and material degradation occurred in the macro-porous scaffold composed of CPC,SP and Col-I sponge(P〈0.05).Conclusion:Modular design of bone substitutes might facilitate their in vivo translation.The combination patterns of SP,Col-I and CPC may affect the final composites bioactivity.The determining factors for scaffold&#39;s osteo-inductivity/conductivity include controlled SP peptides&#39; release and material&#39;s pore structures.
出处 《实用口腔医学杂志》 CSCD 北大核心 2017年第3期297-301,共5页 Journal of Practical Stomatology
基金 国家自然科学基金(编号:83171119)
关键词 骨替代材料 模块化设计 自固化磷酸钙(CPC) Ⅰ型胶原(Col-Ⅰ) P物质(SP) Bone substitute Modular design Bone substitute Modular design
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  • 1章培标,武汉,王新,庄秀丽,景遐斌,陈学思.可降解高分子丙交酯-乙交酯共聚物(PLGA)三维支架的细胞相容性和鼻软骨组织工程[J].组织工程与重建外科杂志,2006,2(2):88-91. 被引量:5
  • 2Bjurholm A,Kreicbergs A,Brodin E,et al.Substance P-and CGRP-immunoreactive nerves in bone.Peptides 1988;9(1):165-171.
  • 3Lundberg P,Lundgren I,Mukohyama H,et al.Vasoactive intestinal peptide(VIP)/ pituitary adenylate cyclase-activating peptide receptor subtypes in mouse caivarial osteoblasts:presence of VIP-2 receptors and differentiation-induced expression of VIP-1 receptors.Endocrinology 2001;142(1):339-347.
  • 4Nicoll RA,Schenker C,Leeman SE.Substance P as a transmitter candidate.Annu Rev Neurosci 1980;3:227-268.
  • 5Fontan J J,Cortright DN,Krause JE,et al.Substance P and neurokinin-1 receptor expression by intrinsic air way neurons in the rat.Am J Physiol Lung Cell Mol Physiol 2000;278(2):344-355.
  • 6Shih C,Bernard GW.Neurogenic substance P stimulates osteogenesis in vitro.Peptides 1997;18(2):323-326.
  • 7Azuma H,Kido J,Ikedo D,et al.Substance P enhances the inhibition of osteoblastic cell differentiation induced by lipopolysaccharide from Porphyromonas gingivalis.J Periodontol 2004;75(7):974-981.
  • 8Goto T,Nakao K,Gunjigake KK,et al.Substance P stimulates late-stage rat osteoblastic bone formation through neurokinin-1 receptors.Neuropeptides 2007;41(1):25-31.
  • 9Hirata K,Tsukkazaki T,Kadowaki A,et al.Transplantation of skin fibroblasts expressing BMP-2 promotes bone repair more effectively than those expressing Runx2.Bone 2003;32(5):502-512.
  • 10Grigoriadis AE,Heersche JN,Abin JE.Differentiation of muscle,fat,cartilage,and bone from progenitor cells present in a bone-drived clonal cell population:effect of dexamethasone.J Cell Biol 1988;106(6):2139-2151.

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