PICOSECOND PULSED 2-PHOTON IMAGING WITH REPETITION RATES OF 200 AND 400 MHZ

We show the viability of high-resolution two-photon fluorescence imagi ng of fixed and live cells by exciting the fluorophores with a train o f near-infrared pulses with duration in the picosecond range. This is exemplified with a compact, diode-pumped Nd:YVO4 laser, emitting train s of 7-ps pulses at a wavelength of 1064 nm, with a repetition rate of 200 MHz at two separate outputs. Incoherent combination of the output s enabled two-photon excitation with a repetition rate of 400 MHz. For a numerical aperture of 1.4 (oil), we used an average illumination po wer of up to 20-40 mW at the sample, The pulses were coupled into a be am scanning microscope, either directly or through a single mode glass fibre. Compared with standard femtosecond titanium-sapphire excitatio n conditions, our experiments were performed with a 2.5 or 5 times hig her repetition rate, 30-70 times longer pulses and 10-35 times lower p ulse peak intensity. The experiments indicate the possibility of signi ficantly relaxing the temporal pulse width constraints for a series of applications.