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contributor authorRamaswamy, Sharan
contributor authorBoronyak, Steven M.
contributor authorLe, Trung
contributor authorHolmes, Andrew
contributor authorSotiropoulos, Fotis
contributor authorSacks, Michael S.
date accessioned2017-05-09T01:05:44Z
date available2017-05-09T01:05:44Z
date issued2014
identifier issn0148-0731
identifier otherbio_136_12_121009.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/154115
description abstractThe 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 (cyclicflexflow) 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 أ— 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 آ±â€‰256 خ¼g/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 CellMediated 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.
publisherThe American Society of Mechanical Engineers (ASME)
titleA Novel Bioreactor for Mechanobiological Studies of Engineered Heart Valve Tissue Formation Under Pulmonary Arterial Physiological Flow Conditions
typeJournal Paper
journal volume136
journal issue12
journal titleJournal of Biomechanical Engineering
identifier doi10.1115/1.4028815
journal fristpage121009
journal lastpage121009
identifier eissn1528-8951
treeJournal of Biomechanical Engineering:;2014:;volume( 136 ):;issue: 012
contenttypeFulltext


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