4.8 Article

Drug-Eluting Microarrays for Cell-Based Screening of Chemical-Induced Apoptosis

期刊

ANALYTICAL CHEMISTRY
卷 83, 期 11, 页码 4118-4125

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ac200267t

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资金

  1. National Institutes of Health [EB009196, DE019024, EB007249, HL092836]
  2. National Science Foundation [DMR0847287]
  3. Office of Naval Research
  4. Grants-in-Aid for Scientific Research [22656187] Funding Source: KAKEN

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Traditional high-throughput screening (HTS) is carried out in centralized facilities that require extensive robotic liquid and plate handling equipment. This model of FITS is restrictive as such facilities are not accessible to many researchers. We have designed a simple microarray platform for cell-based screening that can be carried out at the benchtop. The device creates a microarray of 2100 individual cell-based assays in a standard microscope slide format. A microarray of chemical-laden hydrogels addresses a matching array of cell-laden microwells thus creating a microarray of sealed microscale cell cultures each with unique conditions. We demonstrate the utility of the device by screening the extent of apoptosis and necrosis in MCF-7 breast cancer cells in response to exposure to a small library of chemical compounds. From a set of screens we produced a rank order of chemicals that preferentially induce apoptosis over necrosis in MCF-7 cells. Treatment with doxorubicin induced high levels of apoptosis in comparison with staurosporine, ethanol, and hydrogen peroxide, whereas treatment with 100 mu M ethanol induced minimal apoptosis with high levels of necrosis. We anticipate broad application of the device for various research and discovery applications as it is easy to use, scalable, and can be fabricated and operated with minimal peripheral equipment.

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