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Modeling and Characterization of Polydimethylsiloxane (PDMS) Pillar Arrays for Biological Applications

机译:用于生物应用的聚二甲基硅氧烷(PDMS)柱阵列的建模和表征

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The mechanical interaction force between cells and their neighboring extracellular matrix is believed to be very important in various physiological processes and which can be measured by soft material probes. Polydimethylsiloxane (PDMS) is an important polymeric material widely used in bio-MEMS devices such as micropillar arrays for cellular mechanical force measurements. The accuracy of such a measurement relies on choosing an appropriate material constitutive model for converting the measured structural deformations into corresponding reaction forces. However, although PDMS is a well-known viscoelastic material, many researchers in the past have treated it as a linear elastic material and employed the simple cantilever beam equation to calculate the force from observed deflection, which could result in errors of cellular traction force interpretation. In this paper, the mechanical properties of PDMS were characterized by using uniaxial compression, dynamic mechanical analysis, and nanoindentation tests in both macro- and micro- scales, as well as finite element analysis. A generalized Maxwell model with the use of two exponential terms was used to emulate the mechanical behavior of PDMS at room temperature and the subsequent nanoindentation characterizations. After we found the viscoelastic constitutive law of PDMS, we used it to develop a more accurate model for converting deflection data to cellular traction forces. The results indicate that the linear cantilever beam model could significantly overestimate the cellular forces. Furthermore, in situ cellular traction force evolutions of cardiac myocytes were demonstrated by using this new conversion model. The results presented by this paper are believed to be useful for biologists who are interpreting similar physiological processes.
机译:在各种生理过程中,细胞与它们相邻的细胞外基质之间的机械相互作用力被认为是非常重要的,并且可以通过软材料探针来测量。聚二甲基硅氧烷(PDMS)是一种重要的聚合材料,广泛用于生物MEMS设备(例如用于细胞机械力测量的微柱阵列)中。这种测量的准确性取决于选择适当的材料本构模型,以将测量的结构变形转换为相应的反作用力。然而,尽管PDMS是一种众所周知的粘弹性材料,但过去许多研究人员将其视为线性弹性材料,并使用简单的悬臂梁方程来根据观察到的挠度来计算力,这可能会导致细胞牵引力解释的误差。 。在本文中,PDMS的力学性能通过单轴压缩,动态力学分析,宏观和微观尺度的纳米压痕测试以及有限元分析来表征。使用两个指数项的广义麦克斯韦模型用于模拟PDMS在室温下的力学行为以及随后的纳米压痕表征。在找到PDMS的粘弹性本构定律后,我们用它来开发更精确的模型,以将挠度数据转换为细胞牵引力。结果表明,线性悬臂梁模型可以大大高估细胞力。此外,通过使用这种新的转换模型证明了心肌细胞的原位细胞牵引力演变。相信本文所提供的结果对正在解释相似生理过程的生物学家很有用。

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