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 language | English |
|---|---|
| Pages (from-to) | 1529-1535 |
| Number of pages | 7 |
| Journal | Biosensors and Bioelectronics |
| Volume | 19 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - 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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