A Finite Element Model for Mixed Porohyperelasticity with Transport, Swelling, and Growth

被引:17
|
作者
Armstrong, Michelle Hine [1 ]
Tepole, Adrian Buganza [2 ]
Kuhl, Ellen [2 ]
Simon, Bruce R. [3 ]
Vande Geest, Jonathan P. [1 ,3 ,4 ,5 ,6 ,7 ]
机构
[1] Univ Arizona, Grad Interdisciplinary Program Appl Math, Tucson, AZ USA
[2] Stanford Univ, Dept Mech Engn, Stanford, CA 94305 USA
[3] Univ Arizona, Dept Aerosp & Mech Engn, Tucson, AZ 85721 USA
[4] Univ Arizona, Grad Interdisciplinary Program Biomed Engn, Tucson, AZ USA
[5] Univ Arizona, Inst Biocollaborat Res BIO5, Tucson, AZ 85721 USA
[6] Univ Arizona, Dept Biomed Engn, Tucson, AZ 85721 USA
[7] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA 15219 USA
来源
PLOS ONE | 2016年 / 11卷 / 04期
基金
美国国家科学基金会;
关键词
SMOOTH-MUSCLE CONTRACTION; INTERSTITIAL GROWTH; VOLUMETRIC GROWTH; BIOLOGICAL TISSUE; RESIDUAL-STRESS; ARTERIAL GROWTH; MASS-TRANSPORT; MIXTURE MODEL; SOFT-TISSUES; MECHANICS;
D O I
10.1371/journal.pone.0152806
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The purpose of this manuscript is to establish a unified theory of porohyperelasticity with transport and growth and to demonstrate the capability of this theory using a finite element model developed in MATLAB. We combine the theories of volumetric growth and mixed porohyperelasticity with transport and swelling (MPHETS) to derive a new method that models growth of biological soft tissues. The conservation equations and constitutive equations are developed for both solid-only growth and solid/fluid growth. An axisymmetric finite element framework is introduced for the new theory of growing MPHETS (GMPHETS). To illustrate the capabilities of this model, several example finite element test problems are considered using model geometry and material parameters based on experimental data from a porcine coronary artery. Multiple growth laws are considered, including time-driven, concentrationdriven, and stress-driven growth. Time-driven growth is compared against an exact analytical solution to validate the model. For concentration-dependent growth, changing the diffusivity (representing a change in drug) fundamentally changes growth behavior. We further demonstrate that for stress-dependent, solid-only growth of an artery, growth of an MPHETS model results in a more uniform hoop stress than growth in a hyperelastic model for the same amount of growth time using the same growth law. This may have implications in the context of developing residual stresses in soft tissues under intraluminal pressure. To our knowledge, this manuscript provides the first full description of an MPHETS model with growth. The developed computational framework can be used in concert with novel in-vitro and in-vivo experimental approaches to identify the governing growth laws for various soft tissues.
引用
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页数:35
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