The ability to replicate physiological hemodynamic conditions during in vitro tissue development has been recognized as an important aspect in the development and in vitro assessment of engineered heart valve tissues. Moreover, we have demonstrated that studies aiming to understand mechanical conditioning require separation of the major heart valve deformation loading modes: flow, stretch, and flexure (FSF) (Sacks et al., 2009, "Bioengineering Challenges for Heart Valve Tissue Engineering," Annu. Rev. Biomed. Eng., 11(1), pp. 289–313). To achieve these goals in a novel bioreactor design, we utilized a cylindrical conduit configuration for the conditioning chamber to allow for higher fluid velocities, translating to higher shear stresses on the in situ tissue specimens while retaining laminar flow conditions. Moving boundary computational fluid dynamic (CFD) simulations were performed to predict the flow field under combined cyclic flexure and steady flow (cyclic-flex-flow) states using various combinations of flow rate, and media viscosity. The device was successfully constructed and tested for incubator housing, gas exchange, and sterility. In addition, we performed a pilot experiment using biodegradable polymer scaffolds seeded with bone marrow derived stem cells (BMSCs) at a seeding density of 5 × 106 cells/cm2. The constructs were subjected to combined cyclic flexure (1 Hz frequency) and steady flow (Re = 1376; flow rate of 1.06 l/min (LPM); shear stress in the range of 0–9 dynes/cm2) for 2 weeks to permit physiological shear stress conditions. Assays revealed significantly (P < 0.05) higher amounts of collagen (2051 ± 256 μg/g) at the end of 2 weeks in comparison to similar experiments previously conducted in our laboratory but performed at subphysiological levels of shear stress (<2 dynes/cm2; Engelmayr et al., 2006, "Cyclic Flexure and Laminar Flow Synergistically Accelerate Mesenchymal Stem Cell-Mediated Engineered Tissue Formation: Implications for Engineered Heart Valve Tissues," Biomaterials, 27(36), pp. 6083–6095). The implications of this novel design are that fully coupled or decoupled physiological flow, flexure, and stretch modes of engineered tissue conditioning investigations can be readily accomplished with the inclusion of this device in experimental protocols on engineered heart valve tissue formation.
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December 2014
Research-Article
A Novel Bioreactor for Mechanobiological Studies of Engineered Heart Valve Tissue Formation Under Pulmonary Arterial Physiological Flow Conditions
Sharan Ramaswamy,
Sharan Ramaswamy
Department of Biomedical Engineering,
Tissue Engineered Mechanics, Imaging and
Materials Laboratory,
College of Engineering and Computing,
Miami, FL 33174
Tissue Engineered Mechanics, Imaging and
Materials Laboratory,
College of Engineering and Computing,
Florida International University
,Miami, FL 33174
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Steven M. Boronyak,
Steven M. Boronyak
Department of Biomedical Engineering,
Vanderbilt University
,Nashville, TN 37232
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Trung Le,
Trung Le
Department of Civil Engineering,
St. Anthony Falls Laboratory,
College of Science and Engineering,
St. Anthony Falls Laboratory,
College of Science and Engineering,
University of Minnesota
,Minneapolis, MN 55414
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Andrew Holmes,
Andrew Holmes
Swanson School of Engineering,
University of Pittsburgh
,Pittsburgh, PA 15261
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Fotis Sotiropoulos,
Fotis Sotiropoulos
Department of Civil Engineering,
St. Anthony Falls Laboratory,
College of Science and Engineering,
St. Anthony Falls Laboratory,
College of Science and Engineering,
University of Minnesota
,Minneapolis, MN 55414
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Michael S. Sacks
Michael S. Sacks
1
W. A. “Tex” Moncrief, Jr. Simulation-Based
Engineering Science Chair I,
Professor of Biomedical Engineering,
Department of Biomedical Engineering,
Institute for Computational
Engineering and Sciences (ICES),
201 East 24th Street, ACES 5.438,
1 University Station, C0200,
e-mail: msacks@ices.utexas.edu
Engineering Science Chair I,
Professor of Biomedical Engineering,
Department of Biomedical Engineering,
Institute for Computational
Engineering and Sciences (ICES),
The University of Texas at Austin
,201 East 24th Street, ACES 5.438,
1 University Station, C0200,
Austin, TX 78712-0027
e-mail: msacks@ices.utexas.edu
1Corresponding author.
Search for other works by this author on:
Sharan Ramaswamy
Department of Biomedical Engineering,
Tissue Engineered Mechanics, Imaging and
Materials Laboratory,
College of Engineering and Computing,
Miami, FL 33174
Tissue Engineered Mechanics, Imaging and
Materials Laboratory,
College of Engineering and Computing,
Florida International University
,Miami, FL 33174
Steven M. Boronyak
Department of Biomedical Engineering,
Vanderbilt University
,Nashville, TN 37232
Trung Le
Department of Civil Engineering,
St. Anthony Falls Laboratory,
College of Science and Engineering,
St. Anthony Falls Laboratory,
College of Science and Engineering,
University of Minnesota
,Minneapolis, MN 55414
Andrew Holmes
Swanson School of Engineering,
University of Pittsburgh
,Pittsburgh, PA 15261
Fotis Sotiropoulos
Department of Civil Engineering,
St. Anthony Falls Laboratory,
College of Science and Engineering,
St. Anthony Falls Laboratory,
College of Science and Engineering,
University of Minnesota
,Minneapolis, MN 55414
Michael S. Sacks
W. A. “Tex” Moncrief, Jr. Simulation-Based
Engineering Science Chair I,
Professor of Biomedical Engineering,
Department of Biomedical Engineering,
Institute for Computational
Engineering and Sciences (ICES),
201 East 24th Street, ACES 5.438,
1 University Station, C0200,
e-mail: msacks@ices.utexas.edu
Engineering Science Chair I,
Professor of Biomedical Engineering,
Department of Biomedical Engineering,
Institute for Computational
Engineering and Sciences (ICES),
The University of Texas at Austin
,201 East 24th Street, ACES 5.438,
1 University Station, C0200,
Austin, TX 78712-0027
e-mail: msacks@ices.utexas.edu
1Corresponding author.
Manuscript received July 6, 2013; final manuscript received September 29, 2014; accepted manuscript posted October 16, 2014; published online November 7, 2014. Assoc. Editor: Jonathan Vande Geest.
J Biomech Eng. Dec 2014, 136(12): 121009 (14 pages)
Published Online: December 1, 2014
Article history
Received:
July 6, 2013
Revision Received:
September 29, 2014
Accepted:
October 16, 2014
Citation
Ramaswamy, S., Boronyak, S. M., Le, T., Holmes, A., Sotiropoulos, F., and Sacks, M. S. (December 1, 2014). "A Novel Bioreactor for Mechanobiological Studies of Engineered Heart Valve Tissue Formation Under Pulmonary Arterial Physiological Flow Conditions." ASME. J Biomech Eng. December 2014; 136(12): 121009. https://doi.org/10.1115/1.4028815
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