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Amorphous polyphosphate/amorphous calcium carbonate implant material with enhanced bone healing efficacy in a critical-size defect in rats

机译:在大鼠临界尺寸缺损中具有增强的骨愈合功效的非晶态多磷酸盐/非晶态碳酸钙植入物

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In this study the effect of amorphous calcium carbonate (ACC) microparticles and amorphous calcium polyphosphate (polyP) microparticles (termed aCa-polyP-MP) on bone mineral forming cells/ tissue was investigated in vitro and in vivo. The ACC particles (termed ACC-P-10-MP) were prepared in the presence of Na-polyP. Only the combinations of polyP and ACC microparticles enhanced the proliferation rate of human mesenchymal stem cells (MSCs). Gene expression studies revealed that ACC causes an upregulation of the expression of the cell membrane-associated carbonic anhydrase IX (CA IX; formation of ACC), while the transcript level of the alkaline phosphatase (ALP; liberation of orthophosphate from polyP) changes only relatively little. In contrast, aCa-polyP-MP primarily induces ALP expression. If both components are applied together a strong stimulation of expression of both marker genes is observed. In order to investigate whether ACC also enhances bone regeneration induced by polyP in vivo, the particles were encapsulated into PLGA (poly(D, L-lactide-co-glycolide)) microspheres (diameter similar to 800 mu m) and implanted into rat critical-size calvarial defects. The studies revealed that animals that received aCa-polyP-MP microspheres showed an increased rate of regeneration compared to beta-tri-calcium phosphate (beta-TCP) controls. This effect is even accelerated if microspheres with both aCa-polyP-MP and ACC-P10-MP (1 : 1 weight ratio) are applied, resulting in an almost complete restoration of the defect area after 12 weeks. qRT-PCR analyses of tissue sections through the regeneration zone with microspheres containing both aCa-polyP-MP and ACC-P10-MP revealed a significantly higher upregulation of expression of the marker genes compared to each of the components alone. The Young's moduli for microspheres containing aCa-polyP-MP (1.74 MPa) and aCa-polyP-MP/ ACC-P-10-MP (2.38 MPa) were markedly higher compared to beta-TCP-controls (0.63 mPa). Our results show that the combined application of ACC and Ca-polyP (both in the amorphous state) opens new strategies for the development of regenerative implants for the reconstruction of bone defects.
机译:在这项研究中,在体外和体内研究了无定形碳酸钙(ACC)微粒和无定形聚磷酸钙(polyP)微粒(称为aCa-polyP-MP)对骨矿形成细胞/组织的影响。在Na-polyP存在下制备ACC颗粒(称为ACC-P-10-MP)。只有polyP和ACC微粒的组合才能提高人间充质干细胞(MSC)的增殖速率。基因表达研究表明,ACC引起细胞膜相关碳酸酐酶IX(CA IX; ACC的形成)的表达上调,而碱性磷酸酶(ALP;正磷酸盐从polyP的释放)的转录水平仅相对变化小。相反,aCa-polyP-MP主要诱导ALP表达。如果将两种组分一起使用,则观察到两种标记基因表达的强烈刺激。为了研究ACC是否还增强体内由polyP诱导的骨再生,将颗​​粒封装到PLGA(聚(D,L-丙交酯-乙交酯)乙交酯)微球(直径约800微米)中,并植入大鼠临界大小的颅骨缺损。研究表明,与β-磷酸三钙(β-TCP)对照相比,接受aCa-polyP-MP微球的动物显示出更高的再生速率。如果同时使用同时含有aCa-polyP-MP和ACC-P10-MP(1:1重量比)的微球,则效果会进一步加快,从而在12周后几乎完全恢复缺损区域。用含有aCa-polyP-MP和ACC-P10-MP的微球对通过再生区的组织切片进行qRT-PCR分析显示,与单独使用每种成分相比,标记基因的表达明显更高。与β-TCP对照(0.63 mPa)相比,包含aCa-polyP-MP(1.74 MPa)和aCa-polyP-MP / ACC-P-10-MP(2.38 MPa)的微球的杨氏模量明显更高。我们的结果表明,ACC和Ca-polyP(均处于无定形状态)的联合应用为骨再生修复植入物的开发开辟了新的策略。

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