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Issue 4, 2009
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A multipurpose microfluidic device designed to mimic microenvironment gradients and develop targeted cancer therapeutics

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Abstract

The heterogeneity of cellular microenvironments in tumors severely limits the efficacy of most cancer therapies. We have designed a microfluidic device that mimics the microenvironment gradients present in tumors that will enable the development of more effective cancer therapies. Tumor cell masses were formed within micron-scale chambers exposed to medium perfusion on one side to create linear nutrient gradients. The optical accessibility of the PDMS and glass device enables quantitative transmitted and fluorescence microscopy of all regions of the cell masses. Time-lapse microscopy was used to measure the growth rate and show that the device can be used for long-term efficacy studies. Fluorescence microscopy was used to demonstrate that the cell mass contained viable, apoptotic, and acidic regions similar to in vivo tumors. The diffusion coefficient of doxorubicin was accurately measured, and the accumulation of therapeutic bacteria was quantified. The device is simple to construct, and it can easily be reproduced to create an array of in vitro tumors. Because microenvironment gradients and penetration play critical roles controlling drug efficacy, we believe that this microfluidic device will be vital for understanding the behavior of common cancer drugs in solid tumors and designing novel intratumorally targeted therapeutics.

Graphical abstract: A multipurpose microfluidic device designed to mimic microenvironment gradients and develop targeted cancer therapeutics

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Publication details

The article was received on 27 Jun 2008, accepted on 14 Oct 2008 and first published on 21 Nov 2008


Article type: Paper
DOI: 10.1039/B810571E
Citation: Lab Chip, 2009,9, 545-554
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    A multipurpose microfluidic device designed to mimic microenvironment gradients and develop targeted cancer therapeutics

    C. L. Walsh, B. M. Babin, R. W. Kasinskas, J. A. Foster, M. J. McGarry and N. S. Forbes, Lab Chip, 2009, 9, 545
    DOI: 10.1039/B810571E

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