剪切流动下红细胞-红细胞聚集动力学

M. Abbasi, A. Farutin, H. Ez‐zahraouy, A. Benyoussef, C. Misbah
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引用次数: 8

摘要

悬浮在血浆中的红血球(红细胞)倾向于聚集并形成rouleaux。在聚集过程中,第一阶段是红细胞双体的形成[血细胞、分子和疾病25,339(1999)]。虽然聚集体通常在适度的流动应力下分离,但在某些病理条件下,聚集体变得不可逆,从而导致高血液粘度和血管闭塞。本文采用二维模拟的方法研究了不同条件下剪切流动下的双重态动力学及其对流变学的影响。在参数空间(流动强度、黏附能)的富相图中,我们总结了关于双重态动力学的结果,显示了四种不同类型的双重态结构和动力学。我们发现膜槽踏在双重态分解中起重要作用,与红细胞实验结果一致。这里发现的一个显著特征是,当单个细胞进行翻滚(通过增加囊泡内部粘度)时,由于粘附(即使非常弱)而形成的双偶体即使在非常强的剪切速率下也保持稳定。可以看出,在这种情况下,剪切速率的增加诱导了双重构象的适应,使聚集体能够抵抗细胞-细胞分离。研究表明,随着黏附能的增加,双态悬浮液的归一化有效粘度显著增加,这一事实应该影响微循环中的血液灌注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Erythrocyte-erythrocyte aggregation dynamics under shear flow
Red blood cells (RBCs) -- erythrocytes -- suspended in plasma tend to aggregate and form rouleaux. During aggregation the first stage consists in the formation of RBC doublets [Blood cells, molecules, and diseases 25, 339 (1999)]. While aggregates are normally dissociated by moderate flow stresses, under some pathological conditions the aggregation becomes irreversible, which leads to high blood viscosity and vessel occlusion. We perform here two-dimensional simulations to study the doublet dynamics under shear flow in different conditions and its impact on rheology. We sum up our results on the dynamics of doublet in a rich phase diagram in the parameter space (flow strength, adhesion energy) showing four different types of doublet configurations and dynamics. We find that membrane tank-treading plays an important role in doublet disaggregation, in agreement with experiments on RBCs. A remarkable feature found here is that when a single cell performs tumbling (by increasing vesicle internal viscosity) the doublet formed due to adhesion (even very weak) remains stable even under a very strong shear rate. It is seen in this regime that an increase of shear rate induces an adaptation of the doublet conformation allowing the aggregate to resist cell-cell detachment. We show that the normalized effective viscosity of doublet suspension increases significantly with the adhesion energy, a fact which should affect blood perfusion in microcirculation.
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