首页> 外文期刊>Journal of Biorheology >Measurement and analysis of the shape recovery process of each erythrocyte for estimation of its deformability using the microchannel technique: the influence of the softness of the cell membrane and viscosity of the hemoglobin solution inside the cell
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Measurement and analysis of the shape recovery process of each erythrocyte for estimation of its deformability using the microchannel technique: the influence of the softness of the cell membrane and viscosity of the hemoglobin solution inside the cell

机译:使用微通道技术对每个红细胞的形状恢复过程进行测量和分析,以评估其变形能力:细胞膜柔软度和细胞内血红蛋白溶液粘度的影响

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This study tried to evaluate the deformability of each erythrocyte by measuring the time constant of shape recovery just after the erythrocytes left the microchannels. We fabricated a microchannel array with a 5μm-square, 100μm-long cross-section on a PDMS sheet. Three different kinds of blood samples were prepared-healthy erythrocytes as a control, artificially membrane-hardened erythrocytes and artificial hemoglobin solution-diluted erythrocytes-to investigate the influence of erythrocyte's mechanical property changes on the time constant of shape recovery. These shape recovery processes were modeled and analyzed by a standard liner solid model, As a result, the temporal variation of the compressive strain of all erythrocytes showed exponential decay with time elapsed like a first order lag system, so the time constant of shape recovery could be calculated from the semi-logarithmic relaxation curve. The stiffer the cell membrane was using glutaraldehyde, the shorted the time constant for relaxation became compared to healthy erythrocytes. The diluted hemoglobin erythrocytes snapped back quicker than healthy ones. In addition, the time constant of healthy blood drawn from females was clearly shorter than that collected from males. However, the time constant of fully hemoglobin substituted erythrocytes was not affected by gender difference. These results indicate that there is not a sigr nificant difference in the stiffness of healthy cell membranes regardless of individual and gender differences. On the other hand, the viscosity of the hemoglobin solution inside the cell is one of the significant factors affecting the time constant. Therefore, these results suggest that the deformability of individual erythrocytes can be quantitated by the time constant for relaxation measured by micro-channel techniques.
机译:该研究试图通过在红细胞离开微通道后测量形状恢复的时间常数来评估每个红细胞的可变形性。我们在PDMS板上制作了横截面为5μm正方形,长为100μm的微通道阵列。制备了三种不同的血样,以健康的红细胞为对照,人工膜硬化的红细胞和人工血红蛋白溶液稀释的红细胞,以研究红细胞的机械性能变化对形状恢复时间常数的影响。通过标准线性固体模型对这些形状恢复过程进行建模和分析,结果,与一阶滞后系统一样,所有红细胞压缩应变的时间变化都显示出随着时间的流逝呈指数衰减,因此形状恢复的时间常数可以由半对数弛豫曲线计算。使用戊二醛会使细胞膜变硬,与健康的红细胞相比,松弛时间常数缩短了。稀释的血红蛋白红细胞比健康的红细胞回弹更快。此外,从女性身上抽取的健康血液的时间常数明显短于从男性身上抽取的时间。但是,完全被血红蛋白取代的红细胞的时间常数不受性别差异的影响。这些结果表明,无论个体和性别差异如何,健康细胞膜的硬度均无明显差异。另一方面,细胞内血红蛋白溶液的粘度是影响时间常数的重要因素之一。因此,这些结果表明,可以通过微通道技术测量的弛豫时间常数来量化单个红细胞的变形能力。

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