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A sandwiched microarray platform for benchtop cell-based high throughput screening

  • Jinhui Wu
  • , Ian Wheeldon
  • , Yuqi Guo
  • , Tingli Lu
  • , Yanan Du
  • , Ben Wang
  • , Jiankang He
  • , Yiqiao Hu
  • , Ali Khademhosseini
  • Harvard University
  • Harvard-Massachusetts Institutes of Technology Health Sciences and Technology
  • Nanjing University
  • Zhengzhou University
  • Northwestern Polytechnical University Xian

Research output: Contribution to journal › Article › peer-review

68 Scopus citations

Abstract

The emergence of combinatorial chemistries and the increased discovery of natural compounds have led to the production of expansive libraries of drug candidates and vast numbers of compounds with potentially interesting biological activities. Despite broad interest in high throughput screening (HTS) across varied fields of biological research, there has not been an increase in accessible HTS technologies. Here, we present a simple microarray sandwich system suitable for screening chemical libraries in cell-based assays at the benchtop. The microarray platform delivers chemical compounds to isolated cell cultures by 'sandwiching' chemical-laden arrayed posts with cell-seeded microwells. In this way, an array of sealed cell-based assays was generated without cross-contamination between neighbouring assays. After chemical exposure, cell viability was analyzed by fluorescence detection of cell viability assays on a per microwell basis using a standard microarray scanner. We demonstrate the efficacy of the system by generating four hits from toxicology screens towards MCF-7 human breast cancer cells. Three of the hits were identified in a combinatorial screen of a library of natural compounds in combination with verapamil, a P-glycoprotein inhibitor. A fourth hit, 9-methoxy-camptothecin, was identified by screening the natural compound library in the absence of verapamil. The method developed here miniaturizes existing HTS systems and enables the screening of a wide array of individual or combinatorial libraries in a reproducible and scalable manner. We anticipate broad application of such a system as it is amenable to combinatorial drug screening in a simple, robust and portable platform.

Original languageEnglish
Pages (from-to)841-848
Number of pages8
JournalBiomaterials
Volume32
Issue number3
DOIs
StatePublished - Jan 2011
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Anti-tumour
  • Biomedical
  • Camptothecin
  • Drug screening
  • Microscale engineering
  • Verapamil

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