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Issue 6, 2009
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Rapid generation of spatially and temporally controllable long-range concentration gradients in a microfluidic device

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Abstract

The ability to rapidly generate concentration gradients of diffusible molecules has important applications in many chemical and biological studies. Here we established spatially and temporally controllable concentration gradients of molecules (i.e.proteins or toxins) in a portable microfluidic device in an easy and rapid manner. The formation of the concentration gradients was initiated by a passive-pump-induced forward flow and further optimized during an evaporation-induced backward flow. The centimeter-long gradients along the microfluidic channel were shown to be spatially and temporally controlled by the backward flow. The gradient profile was stabilized by stopping the flow. Computational simulations of this dynamic process illustrated the combined effects of convection and diffusion on the gradient generation, and fit well with the experimental data. To demonstrate the applications of this methodology, a stabilized concentration gradient of a cardiac toxin, alpha-cypermethrin, along the microchannel was used to test the response of HL-1 cardiac cells in the micro-device, which correlated with toxicity data obtained from multi-well plates. The approach presented here may be useful for many biological and chemical processes that require rapid generation of long-range gradients in a portable microfluidic device.

Graphical abstract: Rapid generation of spatially and temporally controllable long-range concentration gradients in a microfluidic device

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Publication details

The article was received on 15 Sep 2008, accepted on 13 Nov 2008 and first published on 10 Dec 2008


Article type: Paper
DOI: 10.1039/B815990D
Citation: Lab Chip, 2009,9, 761-767
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    Rapid generation of spatially and temporally controllable long-range concentration gradients in a microfluidic device

    Y. Du, J. Shim, M. Vidula, M. J. Hancock, E. Lo, B. G. Chung, J. T. Borenstein, M. Khabiry, D. M. Cropek and A. Khademhosseini, Lab Chip, 2009, 9, 761
    DOI: 10.1039/B815990D

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