Abstract
A non-invasive optical method to monitor cellular NADH and probe metabolic activity was illustrated. The autofluorescence intensity differences between cell lines were due to the differing concentrations of protein bound mitochondrial NADH. Fluorescence decays were analyzed by least squares iterative reconvolution to account for instrument response and to extract lifetimes and amplitudes. All data were obtained using an excitation wavelength of 337.1 nm.
Original language | English (US) |
---|---|
Pages | 587-588 |
Number of pages | 2 |
State | Published - 2002 |
Event | Conference on Lasers and Electro-Optics (CLEO 2002) - Long Beach, CA, United States Duration: May 19 2002 → May 24 2002 |
Other
Other | Conference on Lasers and Electro-Optics (CLEO 2002) |
---|---|
Country/Territory | United States |
City | Long Beach, CA |
Period | 5/19/02 → 5/24/02 |
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- Atomic and Molecular Physics, and Optics
- Condensed Matter Physics
- Electrical and Electronic Engineering