The aim of the investigation was to determine a noninvasive range of near-infrared femtosecond laser pulse exposure for mouse oocyte intracellular nanosurgery and to estimate oocyte developmental competence in vitro depending on pulse energy and total exposure time.Materials and Methods. The model object was a preovulatory germinal vesicle mouse oocyte. Femtosecond laser radiation with a central wavelength of 780 nm was utilized in two modes: 1) single pulses with 30 fs duration and pulse energy up to 100 nJ; 2) trains of pulses with 100 fs duration, 80 MHz repetition rate (12.5 ns between pulses) and pulse energy from 0.5 to 2 nJ; total duration of the pulse trains ranged from 15 to 60 ms. Radiation was focused by a microscope objective lens (60×, 0.7 NA). Oocytes were cultured to the metaphase of the second meiotic division, which was used as invasiveness criteria. This stage was detected by polar bodies and metaphase plate formation.Results. The threshold of invasiveness was determined for a single femtosecond pulse exposure. Cytoplasmic membrane rupture and cell disruption occurred under the exposure of a single 30 fs pulse with 100 nJ energy. The cytoplasm and nucleus exposure to femtosecond pulse trains did not induce permanent damage to the oocytes. The rate of gas-vapor bubble formation was measured after the action of pulse trains on the cytoplasm and nucleus chromatin of mammalian oocytes. The pulse energy of 1 nJ is a threshold value for bubble formation in the cytoplasm, and 2 nJ in the nucleus. Exposure to laser pulse trains with 80 MHz repetition rate and 100 fs duration didn't change oocyte ability to achieve metaphase II stage within the studied range of pulse energies and pulse train durations.Conclusion. Surgery with femtosecond pulse trains at 80 MHz repetition rate and pulse energy not more than twice as high as the threshold of cavitation or vapor bubble formation does not affect oocyte development to the metaphase II stage. Femtosecond laser nanosurgery can be regarded as a minimally invasive method of intracellular surgery within the investigated range of pulse energies and exposure times.Key words: intracellular surgery; laser surgery; femtosecond laser; preovulatory oocytes.For contacts: Alina A. Osychenko, e-mail: alina.chemphys@gmail.com
Laser Nanosurgery of Mammalian OocytesNanosurgical operations on the cells and embryos using femtosecond lasers with the wavelength in the near-infrared range is a challenging direction of modern biophotonics. The near-infrared range is in the region of biotissue transparency: it is not absorbed either by the water or organic substances of the cell (proteins, lipids, nucleic acids, carbohydrates) [1]. A high localization of the femtosecond pulse action in the area of laser beam waist (about 10 femtoliters volume) allows one to perform operations inside the cell/embryo on a separate organelle leaving intact the cell environment and causing no damage to the outer membrane [1][2][3]. Non-linear optical absorption of laser pulse energy by the cell material...