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Modeling and simulation of three-dimensional manipulation of viscoelastic folded biological particles considering the nonlinear model of the cell by AFM

机译:粘弹性折叠生物颗粒三维操纵的建模与仿真考虑到AFM电池非线性模型

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摘要

Previous research on biological particles manipulation has taken into account linear cellular models and spherical geometry, Whereas, particles such as bacteria and cancer cells have cylindrical and crushed cylindrical geometry. On the other hand, cell behavior is nonlinear. Therefore, it is important to apply above mentioned models in the manipulation models and to investigate the modes of motion in the cylindrical nanoparticle manipulation to calculate the critical time and forces in order to understand the properties and behavior of these particles. In this paper, we present the analytical nonlinear cellular mechanical models that lead to the extraction of the creep function proportional to the biological particle behavior. Cylindrical and crushed cylindrical geometry considered in manipulation simulation. The cell is modeled with 2nd and 3rd order nonlinear spring and damper which are parallel and series. At the end, 2nd order nonlinear Kelvin selected as the most appropriate model. Comparison with the cell model of power-law and experimental data led to correction coefficients in models. Hereafter, JKR viscoelastic contact model was proposed for nanoparticles with cylindrical and crushed cylindrical geometry. Then, the application of cell models in the contact model and subsequently modeling of the first phase of the manipulation, considering folding factor, has been done. By simulating the main motion modes, including the mode of the slip of the probe tip on the particle, particle's rotation on the surface and the mode of slipping the particle on the surface, the force and critical times were obtained. According to the results, for a particle with a cylindrical geometry, the slip mode of the particle on the surface happens in 505.4 milliseconds and 5 microseconds faster than other modes. Besides, applying the folding factor causes an increase of 7% in the critical time. Because the folded shape of the cell surface causes more disturbance and friction, it requires more time and force to move the particle away and is matched to the physics of the problem. For a particle with a crushed cylindrical geometry, the slip of the probe tip on the particle occurs in 420.7 milliseconds and 10 milliseconds faster than other modes and under the force of 0.7255 micro N and about 71 percent less than the others. Also, the application of the folding factor for this particle contributes to an increase of 24% in critical force and an increase of 11% in the critical time.
机译:以前关于生物粒子操纵的研究已经考虑了线性蜂窝模型和球形几何形状,而诸如细菌和癌细胞的颗粒具有圆柱形和碎圆柱形几何形状。另一方面,细胞行为是非线性的。因此,重要的是在操纵模型中应用上述模型,并研究圆柱形纳米粒子操纵中的运动模式以计算临界时间和力以理解这些颗粒的性质和行为。在本文中,我们介绍了分析非线性细胞机械模型,其导致与生物颗粒行为成比例的蠕变函数的提取。在操纵模拟中考虑圆柱形和碎圆柱几何。该电池用第二和第三订单非线性弹簧和阻尼器进行建模,该空间弹簧和阻尼器是平行的和串联的。最后,2nd订单非线性kelvin被选为最合适的模型。与幂律和实验数据的细胞模型的比较L导出模型中的校正系数。此后,提出了JKR粘弹性接触型号,用于圆柱形和碎圆柱几何形状的纳米颗粒。然后,已经完成了考虑折叠因子的接触模型中的小区模型并随后建模操纵的第一阶段,考虑折叠因子。通过模拟主动动模式,包括探针尖端的滑动模式在颗粒上,粒子在表面上的表面上的旋转和滑动颗粒的模式,得到力和临界时间。根据结果​​,对于具有圆柱形几何形状的颗粒,表面上的粒子的滑动模式发生在505.4毫秒和5微秒上的速度比其他模式更快。此外,施加折叠因子导致临界时间增加7%。因为细胞表面的折叠形状导致更多的干扰和摩擦,所以需要更多的时间和力来移动颗粒并与问题的物理匹配。对于具有碎圆柱几何形状的颗粒,探针尖端的滑动件在颗粒上发生在420.7毫秒和10毫秒的速度,而不是其他模式,并且在0.7255微n的力下,比其他方式约为71%。而且,折叠因子的应用对于临界力的临界力增加到24%,临界时间增加11%。

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