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血液凝块的水力传导率与纤维蛋白和血小板密度的关系。

The hydraulic permeability of blood clots as a function of fibrin and platelet density.

机构信息

Department of Chemical and Biological Engineering, Colorado School of Mines, Golden, Colorado, USA.

出版信息

Biophys J. 2013 Apr 16;104(8):1812-23. doi: 10.1016/j.bpj.2013.02.055.

Abstract

Interstitial fluid flow within blood clots is a biophysical mechanism that regulates clot growth and dissolution. Assuming that a clot can be modeled as a porous medium, the physical property that dictates interstitial fluid flow is the hydraulic permeability. The objective of this study was to bound the possible values of the hydraulic permeability in clots formed in vivo and present relationships that can be used to estimate clot permeability as a function of composition. A series of clots with known densities of fibrin and platelets, the two major components of a clot, were formed under static conditions. The permeability was calculated by measuring the interstitial fluid velocity through the clots at a constant pressure gradient. Fibrin gels formed with a fiber volume fraction of 0.02-0.54 had permeabilities of 1.2 × 10(-1)-1.5 × 10(-4)μm(2). Platelet-rich clots with a platelet volume fraction of 0.01-0.61 and a fibrin volume fraction of 0.03 had permeabilities over a range of 1.1 × 10(-2)-1.5 × 10(-5)μm(2). The permeability of fibrin gels and of clots with platelet volume fraction of <0.2 were modeled as an array of disordered cylinders with uniform diameters. Clots with a platelet volume fraction of >0.2 were modeled as a Brinkman medium of coarse solids (platelets) embedded in a mesh of fine fibers (fibrin). Our data suggest that the permeability of clots formed in vivo can vary by up to five orders of magnitude, with pore sizes that range from 4 to 350 nm. These findings have important implications for the transport of coagulation zymogens/enzymes in the interstitial spaces during clot formation, as well as the design of fibrinolytic drug delivery strategies.

摘要

在血栓内的间质液流动是调节血栓生长和溶解的生物物理机制。假设血栓可以被建模为多孔介质,决定间质液流动的物理性质是水力渗透率。本研究的目的是限制体内形成的血栓的水力渗透率的可能值,并提出可用于估计血栓渗透率作为组成函数的关系。一系列具有已知纤维蛋白和血小板密度的血栓在静态条件下形成,这是血栓的两个主要成分。通过在恒定压力梯度下测量通过血栓的间质液速度来计算渗透率。纤维蛋白凝胶的纤维体积分数为 0.02-0.54,渗透率为 1.2×10(-1)-1.5×10(-4)μm(2)。血小板体积分数为 0.01-0.61 和纤维蛋白体积分数为 0.03 的富含血小板的血栓的渗透率范围为 1.1×10(-2)-1.5×10(-5)μm(2)。纤维蛋白凝胶和血小板体积分数<0.2 的血栓的渗透率被建模为具有均匀直径的无序圆柱阵列。血小板体积分数>0.2 的血栓被建模为嵌入细纤维(纤维蛋白)网格中的粗固体(血小板)的 Brinkman 介质。我们的数据表明,体内形成的血栓的渗透率可能相差五个数量级,孔径范围为 4 至 350nm。这些发现对凝血酶原/酶在血栓形成过程中在间质空间中的转运以及纤维蛋白溶解药物输送策略的设计具有重要意义。

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