Key result
A generalized Maxwell model using two exponential terms accurately emulated the viscoelastic behavior of PDMS, improving the conversion of deflection data to cellular traction forces in cardiac myocytes.
Using a viscoelastic constitutive model rather than a linear elastic model for PDMS improves the accuracy of measuring cellular traction forces in cardiac myocytes.
Viscoelastic PDMS modeling refines myocyte traction force assays; leaves open validation for human cardiac applications.
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, 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, as well as finite element analysis (FEA). A generalized Maxwell model with the use of two exponential terms was used to emulate the mechanical behavior of PDMS at room temperature. 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. Moreover,in situcellular 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.
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Lin et al. (2009) studied this question. Viscoelastic constitutive model for PDMS vs. Linear elastic material model was evaluated on Cellular traction force interpretation. A generalized Maxwell model using two exponential terms accurately emulated the viscoelastic behavior of PDMS, improving the conversion of deflection data to cellular traction forces in cardiac myocytes.
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