To elucidate the mechanism of photosensitization with pulsed light excitation, we previously introduced fluorescence-oxygen diagram that shows the correlation between photochemical oxygen consumption and photobleaching during a treatment (Kawauchi et al., Photochem. Photobiol., 80, 216-223, 2004). In pulsed photodynamic treatment of A549 cells with ATX-S10•Na(II), the diagrams for treatments at relatively high repetition rates of 10 and 30 Hz showed the complex behaviors of photochemical reaction; photobleaching initially occurred with oxygen consumption but it was switched to oxygen-independent photobleaching, which was followed by a secondary oxygen-consuming regime. In this study, fluorescence microscopy revealed that for treatments at 10 and 30 Hz, subcellular fluorescence distribution of ATX-S10•Na(II) changed drastically from the high-intensity spotty patterns showing lysosomal accumulation to the diffusive patterns within the cytosol during certain ranges of total light dose. These ranges were found to coincide with those in which oxygen-independent reaction appeared. These findings suggest that the sensitizer started to be redistributed from lysosomes to the cytosol during the oxygen-independent reaction regime. On the other hand, at 5 Hz, such reaction switching was not clearly seen during whole irradiation period in the diagram; this was consistent with the observation that sensitizer redistribution efficiently occurred even in the early phase of irradiation. The appearance of oxygen-independent reaction at the higher repetition rates may be caused by high local concentration of the sensitizer and the resultant low concentration of oxygen in the reaction sites due to the shorter pulse-to-pulse time intervals. In pulsed photodynamic treatment, pulse frequency is an important parameter that affects the intracellular kinetics of the sensitizer and hence the photochemical reaction dynamics.
[1]
H. Stiel,et al.
Intensity‐Dependent Enzyme Photosensitization Using 532 nm Nanosecond Laser Pulses
,
1996,
Photochemistry and photobiology.
[2]
Satoko Kawauchi,et al.
Correlation Between Oxygen Consumption and Photobleaching During In Vitro Photodynamic Treatment with ATX-S10·Na(II) Using Pulsed Light Excitation: Dependence of Pulse Repetition Rate and Irradiation Time¶
,
2004,
Photochemistry and photobiology.
[3]
A. Andreoni,et al.
Two-step photoactivation of hematoporphyrin by excimer-pumped dye-laser pulses.
,
1987,
Journal of photochemistry and photobiology. B, Biology.
[4]
Christopher S. Foote.
Type I and Type II Mechanisms of Photodynamic Action
,
1987
.
[5]
B. Pogue,et al.
Transient absorption changes in vivo during photodynamic therapy with pulsed-laser light
,
1999,
British Journal of Cancer.
[6]
L. Lindqvist,et al.
Influence of the gel-liquid phase transition on hematoporphyrin triplet deactivation in liposomes.
,
1988,
Journal of photochemistry and photobiology. B, Biology.
[7]
M S Patterson,et al.
Absorbed photodynamic dose from pulsed versus continuous wave light examined with tissue-simulating dosimeters.
,
1997,
Applied optics.