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Indentation Micromechanics of Fibroblast-Populated Fibrin Constructs

机译:成纤维细胞填充纤维蛋白构建体的压痕微机械

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During normal wound healing,a fibrin clot is formed within the first few minutes and is replaced,over several days,by collagen and other extracellular matrix components which are populated with fibroblasts [Clark,1996].This process leads to the rebuilding of dermal tissue on which the epidermal tissue is slowly rebuilt.In severe acute and chronic wounds dermal replacement materials that mimic these processes are needed.Current trends are to use scaffolds as structural substitutes as well as carriers for growth factors and cells for wound treatment.Fibrin-based sealants have been used over the last 30 years in hemostasis and tissue sealing applications and in the last 5 years as a scaffold.Fibrin sealant consists of two primary components,fibrinogen and thrombin which form a fibrin clot when mixed.However,a basic understanding of the microstructure/property relationships of fibrin/collagen constructs is not yet fully established.Furthermore,while previous studies showed that cells proliferate and differentiate within 3D fibrin clots,their effect on structural mechanics of the fibrin clot has not been examined.
机译:在正常伤口愈合期间,在最初的几分钟内形成纤维蛋白凝块,并通过胶原和其他与成纤维细胞填充的细胞外基质组分在几天内被替换为[Clark,1996]。该方法导致真皮组织的重建表皮组织缓慢重建。在严重的急性和慢性伤口需要模仿这些过程的皮肤替代材料。每股趋势是使用支架作为结构替代品以及伤口治疗的生长因子和细胞的载体。基于纤维蛋白在过去30年中使用的密封剂在止血和组织密封应用中使用,并且在过去5年中作为支架。纤维蛋白密封剂由两个主要成分,纤维蛋白原和凝血酶组成,它们在混合时形成纤维蛋白凝块。然而,基本理解纤维蛋白/胶原构建体的微观结构/性质关系尚未完全建立。繁殖,而先前的研究表明细胞遍布在3D纤维蛋白凝块内效率和分化,尚未检查它们对纤维蛋白凝块的结构力学的影响。

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