Keywords
Macrofluidic, controlled flow rate, controlled matrix
Presentation Type
Event
Research Abstract
Traditional cell culture, performed on flat surfaces under static conditions, does not accurately represent physiologic conditions. As an alternative, groups have applied interstitial fluid flow (0.1-2.0 µm/s) through a 3D cell-embedded extracellular matrix (ECM). Cells sense the flow via mechanotransduction, a process by which cells sense mechanical forces and resultantly respond with biochemical signaling. Previous work demonstrates enhanced cell morphogenesis under interstitial flow conditions. However, fluid flow is poorly described within these systems, stressing the need for a well-characterized 3D interstitial flow system. Understanding fluid mechanics within a perfusion system will help elucidate cellular response to flow-induced mechanical forces.
The objective of this study was to quantify the fluid flow velocity through a controlled ECM. The changes in the collagen concentration are directly related to the fibril density of the collagen (stiffness).
A fluorescent Rhodamine solution was pumped at a constant flow rate through a collagen matrix-containing chamber. The resulting flow front was visualized at the center of the chamber using a fluorescent microscope. A Matlab program was developed to track the light intensity between time points to provide measures of flow velocity.
The results suggest that collagen concentration affects the estimated velocity measurements. As collagen fibril density increases, the resistance to flow increases, leading to a decrease in estimated velocity. These results validate the device’s ability to consistently distribute flow over a range of ECM stiffness. Control and quantification of local fluid velocity is essential for future experiments in which cells will be embedded in the collagen matrix to observe cell response to fluid flow.
Session Track
Biotechnology
Recommended Citation
Ana M. Villanueva, Sherry L. Voytik, and Kevin P. Buno,
"Estimating Fluid Local Velocity within a Novel 3D Collagen Matrix Perfusion System"
(August 7, 2014).
The Summer Undergraduate Research Fellowship (SURF) Symposium.
Paper 90.
https://docs.lib.purdue.edu/surf/2014/presentations/90
Estimating Fluid Local Velocity within a Novel 3D Collagen Matrix Perfusion System
Traditional cell culture, performed on flat surfaces under static conditions, does not accurately represent physiologic conditions. As an alternative, groups have applied interstitial fluid flow (0.1-2.0 µm/s) through a 3D cell-embedded extracellular matrix (ECM). Cells sense the flow via mechanotransduction, a process by which cells sense mechanical forces and resultantly respond with biochemical signaling. Previous work demonstrates enhanced cell morphogenesis under interstitial flow conditions. However, fluid flow is poorly described within these systems, stressing the need for a well-characterized 3D interstitial flow system. Understanding fluid mechanics within a perfusion system will help elucidate cellular response to flow-induced mechanical forces.
The objective of this study was to quantify the fluid flow velocity through a controlled ECM. The changes in the collagen concentration are directly related to the fibril density of the collagen (stiffness).
A fluorescent Rhodamine solution was pumped at a constant flow rate through a collagen matrix-containing chamber. The resulting flow front was visualized at the center of the chamber using a fluorescent microscope. A Matlab program was developed to track the light intensity between time points to provide measures of flow velocity.
The results suggest that collagen concentration affects the estimated velocity measurements. As collagen fibril density increases, the resistance to flow increases, leading to a decrease in estimated velocity. These results validate the device’s ability to consistently distribute flow over a range of ECM stiffness. Control and quantification of local fluid velocity is essential for future experiments in which cells will be embedded in the collagen matrix to observe cell response to fluid flow.