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A low-volume platform for cell-respirometric screening based on quenched-luminescence oxygen sensing

  • John Alderman
  • , James Hynes
  • , Suzanne M. Floyd
  • , Jan Krüger
  • , Rosemary O'Connor
  • , Dmitri B. Papkovsky
  • Agilent Technologies

Research output: Contribution to journalArticlepeer-review

Abstract

Cell viability assays represent an important technology in modern cell biology, drug discovery and biotechnology, where currently there is a high demand for simple, sensitive and cost-effective screening methods. We have developed a new methodology and associated tools for cell-based screening assays, which are based on the measurement of the rates of oxygen uptake in cells by luminescence quenching. Sealable microchamber devices matching the footprint of a standard 96-well plate were developed and used in conjunction with long-decay phosphorescent oxygen probes. These devices permit cell non-invasive, real-time monitoring of cellular respiration and a rapid, one-step, kinetic assessment of multiple samples for cell viability, drug/effector action. These assays can be carried out on conventional fluorescence plate readers, they are suitable for different types of cells, including adherent and slow-respiring cells, require small sample volumes and cell numbers, and are amenable for high throughput screening. Monitoring of as little as 300 mammalian cells in 3μl volume has been demonstrated.

Original languageEnglish
Pages (from-to)1529-1535
Number of pages7
JournalBiosensors and Bioelectronics
Volume19
Issue number11
DOIs
Publication statusPublished - 15 Jun 2004

Keywords

  • 3-[4,4-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide
  • Adenosine tri-phosphate
  • ATP
  • Cell-based assays
  • Cell-respirometric screening
  • CRS
  • FBS
  • Fetal bovine serum
  • IL-3
  • Interleukin-3
  • Lactate dehydrogenase
  • LDH
  • MTT
  • Optical oxygen sensing

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