Paper
27 February 2007 Correlation between cell viability and cumulative singlet oxygen luminescence from protoporphyrin IX in varying subcellular localizations
Author Affiliations +
Abstract
Photodynamic therapy (PDT) can be targeted toward different subcellular localizations and it is widely believed different subcellular targets vary in their sensitivity to photobiological damage. In this study, PDT-generated near-infrared singlet oxygen (1O2) luminescence was measured along with cell viability under two different incubation protocols: 5- aminolevulinic acid (ALA) endogenously-induced protoporphyrin IX (PpIX) and exogenous PpIX, at different incubation times. Confocal fluorescence microscopy indicated that ALA-induced PpIX (2 h) localized in the mitochondria, whereas exogenous PpIX (1 h) mainly localized to the plasma membrane. Cell viability was determined at several time points during PDT treatments using colony-forming assays, and the surviving fraction correlated well with cumulative 1O2 luminescence counts under both incubation protocols. Preliminary results indicate the plasma membrane is less sensitive to PDT-generated 1O2 than the mitochondria.
© (2007) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Buhong Li, Mark T. Jarvi, Eduardo H. Moriyama, and Brian C. Wilson "Correlation between cell viability and cumulative singlet oxygen luminescence from protoporphyrin IX in varying subcellular localizations", Proc. SPIE 6427, Optical Methods for Tumor Treatment and Detection: Mechanisms and Techniques in Photodynamic Therapy XVI, 642707 (27 February 2007); https://doi.org/10.1117/12.700674
Lens.org Logo
CITATIONS
Cited by 4 scholarly publications.
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Luminescence

Photodynamic therapy

Plasma

Oxygen

Confocal microscopy

Cancer

Microscopy

Back to Top