Optics Letters · 2005 · 137 citations · 16 references
Natural SciencesBiomedical EngineeringBiophysicsBiophotonicsOpticsPhotonicsCellular ImagingFluorescence ImagingFluorescence MicroscopyMultiphoton MicroscopyOptical ImagingUltrafast OpticsMultiphoton Fluorescence ImagingMultiphoton Fluorescence MicroscopyMultiphoton ImagingTwo-photon Excitation MicroscopyTwo-photon Excited FluorescenceTwo-photon Fluorescence ImagingTwo-photon Fluorescence MicroscopyTwo-photon Microscopy
By introducing spatiotemporal pulse shaping techniques to multiphoton microscopy it is possible to obtain video-rate images with depth resolution similar to point-by-point scanning multiphoton microscopy while mechanically scanning in only one dimension. This is achieved by temporal focusing of the illumination pulse: The pulsed excitation field is compressed as it propagates through the sample, reaching its shortest duration (and highest peak intensity) at the focal plane before stretching again beyond it. This method is applied to produce, in a simple and scalable setup, video-rate two-photon excitation fluorescence images of Drosophila egg chambers with nearly 100,000 effective pixels and 1.5 microm depth resolution.
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Two-Photon Laser Scanning Fluorescence Microscopy
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