Phase space files can store the particle information in one or more planes of radiation particles simulated by the Monte Carlo (MC) method. The secondary calculation method based on phase space files is commonly used to improve the efficiency of MC simulations. However, it is still unclear whether phase space files are applicable for microdosimetric evaluations. In this study, voxel-type and mesh-type monolayer cell population models of different sizes were constructed, and phase space files of secondary electrons generated by photons with different initial energies were obtained using the MC software -- PHITS. The overall average dose caused by the secondary electron phase space files in the region of interest and their microdosimetric distribution within cells were calculated and compared with the results caused by the initial photons under the same geometric conditions. The results showed that the adoption of secondary electron phase space files had almost no impact on the evaluation of macroscopic average dose, with deviations lower than 3% compared to the overall dose caused by the initial photons in the Petri dish. For microdosimetric distributions of the voxel-type model and the two different morphologies of mesh-type cell models, with a macroscopic accumulated dose of 1 mGy, the relative deviation of the cell dose distribution generated by the initial photons and the phase space files was below 10% and the total computation time of phase space files was below 2% of initial photon's. For accumulated doses of 10, 50, and 100 mGy, the relative deviation of the cell nucleus specific energy obtained by secondary electrons and initial photons was greater than 10%. As the size of the culture dish increased, the differences in cell dose distributions also increased, with the root mean square error (RMSE) and coefficient of variation (Cv) of dose distributions both exceeding 30%. In conclusion, this study assessed the effectiveness of the secondary calculation method utilizing phase space files for dose evaluation at the cellular scale. This research offers essential technical support and theoretical foundations for the utilization of this approach in microdosimetric investigations at the cellular level.
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