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Measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting

机译:使用与时间相关的单光子计数在样品平面上测量双光子显微镜的超快激光脉冲持续时间

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摘要

Two-photon microscopy (2PM) has revolutionized biomedical imaging by allowing thin optical sectioning in relatively thick biological specimens. Because dispersive microscope components in 2PM, such as objective lens, can alter temporal laser pulse width (typically being broader at the sample plane), for accurate measurements of two-photon absorption properties, it is important to characterize pulse duration at the sample plane. We present a simple modification to a two-photon microscope light path that allows for second-harmonic-generation-based interferometric autocorrelation measurements to characterize ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting (TCSPC). We show that TCSPC can be used as a simple and versatile method to estimate the zero time delay step value between two adjacent ultrafast laser pulses for these measurements. To demonstrate the utility of this modification, we measured the Coherent Chameleon-Ultra II Ti:sapphire laser pulse width at the sample plane using a air, air, or water-immersion objective lens. At 950-nm two-photon excitation, the measured pulse width was , , and ( , ), respectively.
机译:两光子显微镜(2PM)通过允许在相对厚的生物样本中进行薄光学切片,彻底改变了生物医学成像技术。由于2PM中的色散显微镜组件(例如物镜)可以改变时间激光脉冲宽度(通常在样品平面处较宽),因此对于精确测量双光子吸收特性,重要的是表征样品平面处的脉冲持续时间。我们提出了对双光子显微镜光路的简单修改,该方法允许使用基于二次谐波生成的干涉自相关测量来使用时间相关的单光子计数(TCSPC)表征样品平面上的超快激光脉冲持续时间。我们表明,TCSPC可以用作一种简单通用的方法来估计这些测量的两个相邻超快激光脉冲之间的零时延步进值。为了演示此修改的实用性,我们使用空气,空气或水浸物镜在样品平面上测量了相干Chameleon-Ultra II Ti:蓝宝石激光脉冲宽度。在950 nm双光子激发下,测得的脉冲宽度分别为,和(,)。

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