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A Micromechanics Finite-Strain Constitutive Model of Fibrous Tissue

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Date 2011 Sep 20
PMID 21927506
Citations 13
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Abstract

Biological tissues have unique mechanical properties due to the wavy fibrous collagen and elastin microstructure. In inflation, a vessel easily distends under low pressure but becomes stiffer when the fibers are straightened to take up the load. The current microstructural models of blood vessels assume affine deformation; i.e., the deformation of each fiber is assumed to be identical to the macroscopic deformation of the tissue. This uniform-field (UF) assumption leads to the macroscopic (or effective) strain energy of the tissue that is the volumetric sum of the contributions of the tissue components. Here, a micromechanics-based constitutive model of fibrous tissue is developed to remove the affine assumption and to take into consideration the heterogeneous interactions between the fibers and the ground substance. The development is based on the framework of a recently developed second-order homogenization theory, and takes into account the waviness, orientations, and spatial distribution of the fibers, as well as the material nonlinearity at finite-strain deformation. In an illustrative simulation, the predictions of the macroscopic stress-strain relation, and the statistical deformation of the fibers are compared to the UF model, as well as finite-element (FE) simulation. Our predictions agree well with the FE results, while the UF predictions significantly overestimate. The effects of fiber distribution and waviness on the macroscopic stress-strain relation are also investigated. The present mathematical model may serves as a foundation for native as well as for engineered tissues and biomaterials.

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References
1.
Humphrey J, Yin F . A new constitutive formulation for characterizing the mechanical behavior of soft tissues. Biophys J. 1987; 52(4):563-70. PMC: 1330046. DOI: 10.1016/S0006-3495(87)83245-9. View

2.
Oka S . Some theoretical studies on hemorheology. Adv Biophys. 1972; 3:97-160. View

3.
Azuma T, Hasegawa M . A rheological approach to the architecture of arterial walls. Jpn J Physiol. 1971; 21(1):27-47. DOI: 10.2170/jjphysiol.21.27. View

4.
Gosline J, Lillie M, Carrington E, Guerette P, Ortlepp C, Savage K . Elastic proteins: biological roles and mechanical properties. Philos Trans R Soc Lond B Biol Sci. 2002; 357(1418):121-32. PMC: 1692928. DOI: 10.1098/rstb.2001.1022. View

5.
Zulliger M, Fridez P, Hayashi K, Stergiopulos N . A strain energy function for arteries accounting for wall composition and structure. J Biomech. 2004; 37(7):989-1000. DOI: 10.1016/j.jbiomech.2003.11.026. View