Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Acta Biomater. 2018 Apr 15;71:388-397. doi: 10.1016/j.actbio.2018.02.017. Epub 2018 Mar 1.
Precise and accurate measurement of viscoelastic mechanical properties becomes increasingly challenging as sample stiffness decreases to elastic moduli <1 kPa, largely due to difficulties detecting initial contact with the compliant sample surface. This limitation is particularly relevant to characterization of biological soft tissues and compliant gels. Here, we employ impact indentation which, in contrast to shear rheology and conventional indentation, does not require contact detection a priori, and present a novel method to extract viscoelastic moduli and relaxation time constants directly from the impact response. We first validate our approach by using both impact indentation and shear rheology to characterize polydimethylsiloxane (PDMS) elastomers of stiffness ranging from 100 s of Pa to nearly 10 kPa. Assuming a linear viscoelastic constitutive model for the material, we find that the moduli and relaxation times obtained from fitting the impact response agree well with those obtained from fitting the rheological response. Next, we demonstrate our validated method on hydrated, biological soft tissues obtained from porcine brain, murine liver, and murine heart, and report the equilibrium shear moduli, instantaneous shear moduli, and relaxation time constants for each tissue. Together, our findings provide a new and straightforward approach capable of probing local mechanical properties of highly compliant viscoelastic materials with millimeter scale spatial resolution, mitigating complications involving contact detection or sample geometric constraints.
Characterization and optimization of mechanical properties can be essential for the proper function of biomaterials in diverse applications. However, precise and accurate measurement of viscoelastic mechanical properties becomes increasingly difficult with increased compliance (particularly for elastic moduli <1 kPa), largely due to challenges detecting initial contact with the compliant sample surface and measuring response at short timescale or high frequency. By contrast, impact indentation has highly accurate contact detection and can be used to measure short timescale (glassy) response. Here, we demonstrate an experimental and analytical method that confers significant advantages over existing approaches to extract spatially resolved viscoelastic moduli and characteristic time constants of biological tissues (e.g., brain and heart) and engineered biomaterials.
随着样品刚度降低到弹性模量<1kPa,对粘弹性力学性能进行精确和准确的测量变得越来越具有挑战性,这主要是由于难以检测与柔软样品表面的初始接触。这一限制对于生物软组织和柔软凝胶的特性化尤其相关。在这里,我们采用冲击压痕,与剪切流变和传统压痕相比,它不需要预先检测接触,并且提出了一种从冲击响应中直接提取粘弹性模量和松弛时间常数的新方法。我们首先通过使用冲击压痕和剪切流变学来表征从 100 多帕到近 10kPa 的刚度的聚二甲基硅氧烷(PDMS)弹性体,验证了我们的方法。假设材料的线性粘弹性本构模型,我们发现从冲击响应拟合得到的模量和松弛时间与从流变响应拟合得到的模量和松弛时间非常吻合。接下来,我们将经过验证的方法应用于从猪脑、鼠肝和鼠心获得的水合生物软组织,并报告了每种组织的平衡剪切模量、瞬时剪切模量和松弛时间常数。总的来说,我们的发现提供了一种新的、简单的方法,能够以毫米级空间分辨率探测高度柔软的粘弹性材料的局部力学性能,减轻了涉及接触检测或样品几何约束的复杂性。
在各种应用中,对机械性能的特性化和优化对于生物材料的正常功能可能至关重要。然而,随着柔顺性的增加(特别是对于弹性模量<1kPa),对粘弹性力学性能进行精确和准确的测量变得越来越困难,这主要是由于难以检测与柔软样品表面的初始接触以及在短时间尺度或高频下测量响应的挑战。相比之下,冲击压痕具有高度精确的接触检测功能,可用于测量短时间尺度(玻璃态)响应。在这里,我们展示了一种实验和分析方法,与现有方法相比,该方法在提取生物组织(例如脑和心脏)和工程生物材料的空间分辨粘弹性模量和特征时间常数方面具有显著优势。