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Permeability of Three-Dimensional Fibrin Constructs Corresponds to Fibrinogen and Thrombin Concentrations

机译:三维纤维蛋白构建体的渗透性与纤维蛋白原和凝血酶浓度相对应

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摘要

Research in the last few years have focused on the use of three-dimensional (3D) fibrin construct to deliver growth factors and cells. Three-dimensional construct permeability and porosity are important aspects for proper nutrient uptake, gas exchange, and waste removal—factors that are critical for cell growth and survival. We have previously reported that the mechanical strength (stiffness) of 3D fibrin constructs is dependent on the fibrinogen and thrombin concentration. In this study, we established two new in vitro models to examine how fibrin composition affects the final 3D fibrin construct permeability and pore size; thereby, influencing the diffusivity of macromolecules throughout the network of fibrin fibrils. Flow measurements of both liquid and fluoresceinated-dextran microparticles are conducted to calculate the permeability and pore size of 3D fibrin constructs of different fibrinogen and thrombin concentrations. Similarly, the diffusivity of liquid and fluoresceinated-dextran microparticles through these 3D fibrin constructs are determined through diffusion models. Data from these studies show that the structural permeability and pore size of 3D fibrin constructs directly correlate to fibrinogen and thrombin concentration in the final 3D fibrin construct. More specifically, at a constant thrombin concentration of 2 or 5 μ/mL, pore size of the 3D fibrin constructs is dependent on fibrinogen if the concentration is 5 mg/mL and to a lesser extent if the concentration is 10–15 mg/mL. These findings suggest that fibrin's diffusive property can be manipulated to fabricate 3D constructs that are optimized for cellular growth, protein transport, and for the controlled delivery of bioactive molecules such as growth factors.
机译:最近几年的研究集中在使用三维(3D)纤维蛋白构建体传递生长因子和细胞方面。三维构造物的渗透性和孔隙度是适当吸收养分,气体交换和废物清除的重要方面,这些因素对于细胞生长和存活至关重要。先前我们已经报道过3D纤维蛋白构建体的机械强度(刚度)取决于纤维蛋白原和凝血酶的浓度。在这项研究中,我们建立了两个新的体外模型,以检查血纤蛋白成分如何影响最终的3D血纤蛋白构建体的渗透性和孔径;因此,影响大分子在纤维蛋白原纤维网络中的扩散性。进行液体和氟化葡聚糖微粒的流量测量,以计算不同纤维蛋白原和凝血酶浓度的3D纤维蛋白构建体的渗透性和孔径。类似地,通过扩散模型确定液体和氟化葡聚糖微粒通过这些3D纤维蛋白构建体的扩散率。这些研究的数据表明,3D纤维蛋白构建体的结构渗透性和孔径与最终3D纤维蛋白构建体中的纤维蛋白原和凝血酶浓度直接相关。更具体地说,在恒定的凝血酶浓度为2或5μg/ mL时,如果浓度为5μg/ mL,则3D纤维蛋白构建体的孔径取决于血纤蛋白原,而在浓度为10–15μg / mL时,其孔径较小。 。这些发现表明,可以操纵纤维蛋白的扩散特性来制造针对细胞生长,蛋白质运输以及生物活性分子(例如生长因子)的受控递送而优化的3D构建体。

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