Pancreatic cancer is characterized by a particularly poor prognosis. Existing treatment options often fail to achieve adequate efficacy, so there remains a significant need to develop new, more effective treatment approaches. Electrochemotherapy (ECT) represents a promising therapeutic method based on the use of reversible electroporation to temporarily increase the permeability of cell membranes, thereby enabling more effective delivery of cytostatic drugs into cells and consequently potentiating their cytotoxic effect. BOLD-100, a ruthenium-based cytostatic agent that demonstrates high antitumor efficacy in clinical studies, has not yet been tested in combination with ECT. In this master’s thesis, we therefore sought to evaluate the effect of BOLD-100 in combination with ECT under in vitro conditions on the PANC1 pancreatic cancer cell line. We compared the effect of BOLD-100 with the cytostatic agent cisplatin (CDDP), which is routinely used in clinical ECT. We exposed the cells to various concentrations of BOLD-100 and cisplatin with or without electroporation. Cell viability was determined using the PrestoBlue assay 1, 3, and 7 days after treatment. Based on the obtained data, we calculated IC30, IC50, and IC70 and performed a statistical analysis using a two-factor ANOVA test. The results indicate a strong potentiation of the effect of BOLD-100. The cytotoxic effect is rapid; a decrease in cell viability was observed as early as the first day after ECT. The effect further intensified over time, with the lowest IC50 values reached on the seventh day after exposure. Without ECT, the BOLD-100 compound did not significantly affect cell survival. ECT also potentiated the effect of CDDP, but the cytotoxic effects were slower and less pronounced compared to BOLD-100. The results suggest that BOLD-100 ECT could represent an effective alternative to existing therapies, particularly for tumors with developed resistance to cisplatin.
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