Two-photon excitation
photodynamic therapy (TPE-
PDT) is being developed as an improved treatment for
retinal diseases. TPE-
PDT has advantages over one-photon
PDT, including lower collateral damage to healthy tissue and more precise delivery of
PDT. As with one-photon
PDT, there can be local photochemical depletion of
oxygen during TPE-
PDT. Here, we investigate model systems and live cells to measure local
photosensitizer photobleaching and through it, infer local oxygen consumption in therapeutic volumes of the order 1 microm3. Multilamellar vesicles (MLV) and African green monkey kidney (CV-1) cells were used to study the TPE photobleaching dynamics of the
photosensitizer,
Verteporfin. It was found that in an
oxygen-rich environment, photobleaching kinetics could not be modeled using a mono-exponential function, whereas in hypoxic conditions a mono-exponential decay was adequate to represent photobleaching. A biexponential was found to adequately model the
oxygen-rich conditions and it is hypothesized that the fast part of the decay is
oxygen-dependent, whereas the slower rate constant is largely
oxygen-independent. Photobleaching recovery studies in the
CV-1 cells support this hypothesis.