Cerenkov radiation
(CR) can be used as an internal light source
in photodynamic therapy (PDT). Methotrexate (MTX) and paclitaxel (PTX),
chemotherapeutic agents with wide clinical use, have characteristics
of photosensitizers (PS). This work evaluates the possibility of photoexciting
MTX and PTX with CR from
18
F-FDG to produce reactive oxygen
species (ROS) capable of inducing cytotoxicity. PTX did not produce
ROS when excited by CR from
18
F-FDG, so it is not useful
for PDT. In contrast, MTX produces
1
O
2
(detected
by ABMA) in amounts sufficient to significantly decrease the viability
of the T47D cells. MTX solutions of 100 nM combined with
18
F-FDG activities of 50 (1.85 MBq) and 100 μCi (3.7 MBq) produced
a significant decrease in cell viability to (50.09 ± 4.95) and
(47.96 ± 11.19)%, respectively, compared to MTX (66.29 ±
5.92)% and
18
F-FDG (91.35 ± 7.00% for 50 μCi
and 99.43 ± 11.03% for 100 μCi) alone. Using the CellRox
Green reagent, the intracellular production of ROS was confirmed as
the main mechanism of cytotoxicity. The results confirm the therapeutic
potential of photoactivation with CR and the synergy of the combined
treatment with chemotherapy + photodynamic therapy (CMT + PDT). The
combination of chemotherapeutic agents with PS properties and β-emitting
radiopharmaceuticals, previously approved for clinical use, will make
it possible to shorten the evaluation stages of new CMT + PDT systems.