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Computational Growth and Remodeling Model for Evolving Tissue Engineered Vascular Grafts in the Venous Circulation

[+] Author Affiliations
Kristin S. Miller, Brooks V. Udelsman, Jay D. Humphrey

Yale University, New Haven, CT

Yong-Ung Lee, Christopher K. Breuer

Nationwide Children’s Hospital, Columbus, OH

Yuji Naito

Texas Children’s Hospital, Baylor College of Medicine, Houston, TX

Paper No. FMD2013-16168, pp. V001T07A004; 2 pages
doi:10.1115/FMD2013-16168
From:
  • ASME 2013 Conference on Frontiers in Medical Devices: Applications of Computer Modeling and Simulation
  • ASME 2013 Conference on Frontiers in Medical Devices: Applications of Computer Modeling and Simulation
  • Washington, DC, USA, September 11–13, 2013
  • Conference Sponsors: Bioengineering Division
  • ISBN: 978-0-7918-5600-0
  • Copyright © 2013 by ASME

abstract

The field of vascular tissue engineering continues to advance rapidly, yet there is a pressing need to understand better the time course of polymer degradation and the sequence of cell-mediated matrix deposition and organization. Mounting evidence suggests that cells respond to mechanical perturbations through a process of growth and remodeling (G&R) to establish, maintain, and restore a preferred state of homeostatic stress. Previous computational models utilizing G&R approaches have captured arterial responses to diverse changes in mechanical loading [1, 8, 9]. Recently, a G&R framework was also introduced to account for the kinetics of polymer degradation as well as synthesis and degradation of neotissue constituents [5]. Niklason et al. demonstrated that models of G&R can predict both evolving tissue composition and mechanical behavior after extended periods of in vitro culture of polymer-based tissue-engineered vascular grafts (TEVGs), thus providing insights into the timecourse of neotissue formation and polymer removal. Moreover, they suggest that models of G&R can be powerful tools for the future refinement and optimization of scaffold designs. Nevertheless, such computational models have not yet been developed for examining the formation of neotissue following the implantation of a polymeric TEVG in vivo.

Copyright © 2013 by ASME

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