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Issue 5, 2008
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Microcirculation within grooved substrates regulates cell positioning and cell docking inside microfluidic channels

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Abstract

Immobilization of cells inside microfluidic devices is a promising approach for enabling studies related to drug screening and cell biology. Despite extensive studies in using grooved substrates for immobilizing cells inside channels, a systematic study of the effects of various parameters that influence cell docking and retention within grooved substrates has not been performed. We demonstrate using computational simulations that the fluid dynamic environment within microgrooves significantly varies with groove width, generating microcirculation areas in smaller microgrooves. Wall shear stress simulation predicted that shear stresses were in the opposite direction in smaller grooves (25 and 50 μm wide) in comparison to those in wider grooves (75 and 100 μm wide). To validate the simulations, cells were seeded within microfluidic devices, where microgrooves of different widths were aligned perpendicularly to the direction of the flow. Experimental results showed that, as predicted, the inversion of the local direction of shear stress within the smaller grooves resulted in alignment of cells on two opposite sides of the grooves under the same flow conditions. Also, the amplitude of shear stress within microgrooved channels significantly influenced cell retainment in the channels. Therefore, our studies suggest that microscale shear stresses greatly influence cellular docking, immobilization, and retention in fluidic systems and should be considered for the design of cell-based microdevices.

Graphical abstract: Microcirculation within grooved substrates regulates cell positioning and cell docking inside microfluidic channels

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Article information


Submitted
27 Nov 2007
Accepted
10 Mar 2008
First published
04 Apr 2008

Lab Chip, 2008,8, 747-754
Article type
Paper

Microcirculation within grooved substrates regulates cell positioning and cell docking inside microfluidic channels

A. Manbachi, S. Shrivastava, M. Cioffi, B. G. Chung, M. Moretti, U. Demirci, M. Yliperttula and A. Khademhosseini, Lab Chip, 2008, 8, 747
DOI: 10.1039/B718212K

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