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MECHANICAL PROPERTIES OF COLLAGEN, FIBRIN AND COLLAGEN-FIBRIN NETWORKS

机译:胶原蛋白,纤维蛋白和胶原纤维蛋白网络的力学性能

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The macroscopic mechanical properties of bio-engineered tissues are inextricably linked to their microstructure. Often, their microstructure is a complex arrangement of several different components (e.g. collagen, fibrin) that interact with each other to give a tissue its overall properties. These microstructural complexities are further compounded by the dynamic cell interactions with the extracellular matrix (ECM). Our group [1] uses fibrin as the starting scaffold material for cell seeding and tissue growth; over time, the underlying microstructure undergoes dynamic remodeling as the fibrin network is degraded and gradually replaced with collagen. Currently, we have a modeling framework that incorporates a single-component microstructure network to predict the mechanical properties of the engineered tissue [2]. However, this model is unable to capture the transient intermediate stages of tissue growth, during which the tissue is composed of interpenetrating collagen and fibrin networks at varying compositions. In this work, we have incorporated a second network into our model and compared these modeling results with experimental data obtained from uniaxial tests on acellular collagen-fibrin co-gels. This work represents one step in the progression of our model to capture better the relationships between tissue microstructure and macroscopic mechanical properties, with the ultimate goal of developing a comprehensive model framework for rational design of functional engineered tissues.
机译:生物工程组织的宏观力学性能与其微观结构密不可分地连接。通常,它们的微观结构是几种不同的组分(例如胶原蛋白,纤维蛋白)的复杂布置,其相互作用,以给予组织其整体性质。通过与细胞外基质(ECM)的动态细胞相互作用进一步混合这些微观结构复杂性。我们的组[1]用纤维蛋白作为用于细胞播种和组织生长的起始支架材料;随着时间的推移,随着纤维蛋白网络降解并逐渐用胶原蛋白逐渐取代,潜在的微观结构经历动态重塑。目前,我们具有一种建模框架,其包括单组分微结构网络以预测工程化组织的机械性能[2]。然而,该模型不能捕获组织生长的瞬态中间阶段,在此期间组织由不同组合物的互穿胶原蛋白和纤维蛋白网络组成。在这项工作中,我们将第二个网络纳入我们的模型,并将这些建模结果与从单轴试验上获得的无细胞胶原纤维蛋白共凝胶的实验数据进行了比较。这项工作代表了我们模型进展的一步,以捕获组织微观结构和宏观力学性能之间的关系,具有开发功能性工程组织合理设计综合模型框架的最终目标。

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