A new constitutive model for elastic, proximal pulmonary artery tissue is presented here, called the total crimped fiber model. This model is based on the material and microstructural properties of the two main, passive, load-bearing components of the artery wall, elastin, and collagen. Elastin matrix proteins are modeled with an orthotropic neo-Hookean material. High stretch behavior is governed by an orthotropic crimped fiber material modeled as a planar sinusoidal linear elastic beam, which represents collagen fiber deformations. Collagen-dependent artery orthotropy is defined by a structure tensor representing the effective orientation distribution of collagen fiber bundles. Therefore, every parameter of the total crimped fiber model is correlated with either a physiologic structure or geometry or is a mechanically measured material property of the composite tissue. Further, by incorporating elastin orthotropy, this model better represents the mechanics of arterial tissue deformation. These advancements result in a microstructural total crimped fiber model of pulmonary artery tissue mechanics, which demonstrates good quality of fit and flexibility for modeling varied mechanical behaviors encountered in disease states.
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A Microstructurally Driven Model for Pulmonary Artery Tissue
Philip H. Kao,
Philip H. Kao
Department of Mechanical Engineering,
University of Colorado
, Boulder, CO 80309
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Steven R. Lammers,
Steven R. Lammers
Department of Mechanical Engineering,
University of Colorado
, Boulder, CO 80309
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Lian Tian,
Lian Tian
Department of Mechanical Engineering,
University of Colorado
, Boulder, CO 80309
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Kendall Hunter,
Kendall Hunter
Department of Pediatric Cardiology,
University of Colorado Health Sciences
, Denver, CO 80002
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Kurt R. Stenmark,
Kurt R. Stenmark
Department of Pediatrics, Developmental Lung Biology Laboratory,
University of Colorado Health Sciences
, Denver, CO 80002
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Robin Shandas,
Robin Shandas
Department of Mechanical Engineering,
University of Colorado
, Boulder, CO 80309; Center for Bioengineering, University of Colorado
, Anschutz Medical Campus, Aurora, CO 80015
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H. Jerry Qi
H. Jerry Qi
Department of Mechanical Engineering,
e-mail: qih@colorado.edu
University of Colorado
, Boulder, CO 80309
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Philip H. Kao
Department of Mechanical Engineering,
University of Colorado
, Boulder, CO 80309
Steven R. Lammers
Department of Mechanical Engineering,
University of Colorado
, Boulder, CO 80309
Lian Tian
Department of Mechanical Engineering,
University of Colorado
, Boulder, CO 80309
Kendall Hunter
Department of Pediatric Cardiology,
University of Colorado Health Sciences
, Denver, CO 80002
Kurt R. Stenmark
Department of Pediatrics, Developmental Lung Biology Laboratory,
University of Colorado Health Sciences
, Denver, CO 80002
Robin Shandas
Department of Mechanical Engineering,
University of Colorado
, Boulder, CO 80309; Center for Bioengineering, University of Colorado
, Anschutz Medical Campus, Aurora, CO 80015
H. Jerry Qi
Department of Mechanical Engineering,
University of Colorado
, Boulder, CO 80309e-mail: qih@colorado.edu
J Biomech Eng. May 2011, 133(5): 051002 (12 pages)
Published Online: April 8, 2011
Article history
Received:
July 26, 2009
Revised:
August 23, 2010
Posted:
October 4, 2010
Published:
April 8, 2011
Online:
April 8, 2011
Citation
Kao, P. H., Lammers, S. R., Tian, L., Hunter, K., Stenmark, K. R., Shandas, R., and Qi, H. J. (April 8, 2011). "A Microstructurally Driven Model for Pulmonary Artery Tissue." ASME. J Biomech Eng. May 2011; 133(5): 051002. https://doi.org/10.1115/1.4002698
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