Objective: The purpose of this study was to investigate the possible cytotoxic and genotoxic impact of new-generation 206 nm femtosecond solid-state laser irradiation on murine skin cells in vitro, and to compare the cell and DNA damage caused by different wavelength (206 vs. 257 nm) femtosecond laser pulses. Background data: The first attempts to evaluate the possible genotoxic impact of ultrashort laser pulses on the murine bone marrow cells in vitro revealed the unlooked-for DNA-damaging effect. However, the impact of far-ultraviolet (UV) radiation on genetic material of internal and external organs' cells may differ due to differences in size, structure, and biochemical composition of the cells. Methods: Mouse skin cells were exposed to different doses of 206 and 257 nm wavelength femtosecond laser, and 254 nm UV lamp irradiation. Comet assay in two versions-the standard alkaline and the enzyme-linked-was used for the evaluation of DNA damage. Results: The irradiation determined by different parameters demonstrated intensity-dependent genotoxic impact. The pyrimidine dimers made up the greater part of DNA photodamage, but with rising exposure dose the increase of relative amount of more energy-consuming primary damage-DNA strand breaks-was detected. Conclusions: The 206 nm femtosecond laser irradiation was much more cytotoxic but caused less primary DNA damage than the same pulse duration longer wavelength (257 nm) laser irradiation. DNA-damaging effect of 206 nm femtosecond laser pulses with extremely low penetration force may highly depend on the size, structure, and biochemical composition of the cells of organ or tissue targets.
Keywords: Comet assay; DNA photodamage; femtosecond UV laser; genotoxic impact; skin cells.