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Improved depth resolution in video-rate line-scanning multiphoton microscopy using temporal focusing

机译:使用时间聚焦提高了视频速率线扫描多光子显微镜的深度分辨率

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摘要

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 (mu)m depth resolution.
机译:通过将时空脉冲整形技术引入多光子显微镜,可以在仅进行一维机械扫描的同时,获得具有类似于逐点扫描多光子显微镜的深度分辨率的视频速率图像。这是通过对照明脉冲进行时间聚焦来实现的:脉冲激发场在其传播通过样本时被压缩,在焦平面处达到其最短持续时间(和最高峰值强度),然后再次拉伸超过其范围。该方法用于以简单且可扩展的设置生成果蝇卵室的视频速率双光子激发荧光图像,其有效像素接近100,000,深度分辨率为1.5μm。

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