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首页> 外文期刊>International journal for numerical methods in biomedical engineering >The dynamics of a healthy and infected red blood cell in flow through constricted channels: A DPD simulation
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The dynamics of a healthy and infected red blood cell in flow through constricted channels: A DPD simulation

机译:通过狭窄通道流动的健康且受感染的红细胞的动力学:DPD模拟

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Understanding the dynamics of red blood cell (RBC) motion under in silico conditions is central to the development of cost-effective diagnostic tools. Specifically, unraveling the relationship between the rheological properties and the nature of shape change in the RBC (healthy or infected) can be extremely useful. In case of malarial infection, RBC progressively loses its deformability and tends to occlude the microvessel. In the present study, detailed mesoscopic simulations are performed to investigate the deformation dynamics of an RBC in flow through a constricted channel. Specifically, the manifestation of viscous forces (through flow rates) on the passage and blockage characteristics of a healthy red blood cell (hRBC) vis-a-vis an infected red blood cell (iRBC) are investigated. A finite-sized dissipative particle dynamics framework is used to model plasma in conjunction with a discrete model for the RBC. Instantaneous wall boundary method was used to model no-slip wall boundary conditions with a good control on the near-wall density fluctuations and compressibility effects. To investigate the microvascular occlusion, the RBC motion through 2 types of constricted channels, viz, (1) a tapered microchannel and (2) a stenosed-type microchannel, were simulated. It was observed that the deformation of an infected cell was much less compared with a healthy cell, with an attendant increase in the passage time. Apart from the qualitative features, deformation indices were obtained. The deformation of hRBC was sudden, while the iRBC deformed slowly as it traversed through the constriction. For higher flow rates, both hRBC and iRBC were found to undergo severe deformation. Even under low flow rates, hRBC could easily traverse past the constricted channel. However, for sufficiently slow flow rates (eg, capillary flows), the microchannel was found to be completely blocked by the iRBC.
机译:了解计算机条件下的红细胞(RBC)运动的动态是开发具有成本效益的诊断工具的关键。具体来说,揭露流变性质与RBC(健康或感染)中RBC形状变化的性质之间的关系非常有用。如果发生疟疾感染,RBC会逐渐失去其可变形性,并倾向于阻塞微血管。在本研究中,进行了详细的介观模拟,以研究流经狭窄通道的RBC的变形动力学。具体地,研究了相对于被感染的红细胞(iRBC),健康的红细胞(hRBC)的通过和阻断特性上的粘性力(通过流速)的表现。有限尺寸的耗散粒子动力学框架用于结合RBC的离散模型对等离子体进行建模。瞬时壁边界方法被用来模拟防滑壁边界条件,并很好地控制了近壁密度波动和可压缩性。为了研究微血管阻塞,模拟了通过两种类型的收缩通道的红细胞运动,即,(1)锥形微通道和(2)狭窄型微通道。观察到,与健康细胞相比,被感染细胞的变形要小得多,伴随着传代时间的增加。除了定性特征,还获得了变形指标。 hRBC的变形是突然的,而iRBC穿过颈缩时变形缓慢。对于更高的流速,发现hRBC和iRBC都发生严重变形。即使在低流速下,hRBC仍可轻松穿越狭窄的通道。但是,对于足够慢的流速(例如毛细管流),发现微通道被iRBC完全堵塞。

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