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High-resolution imaging in two-photon excitation microscopy using in situ estimations of the point spread function

机译:使用点扩散函数的原位估计在双光子激发显微镜中进行高分辨率成像

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We present a technique for improving the spatial resolution of two-photon excitation microscopy; our technique combines annular illumination with an in situ estimation of the point spread function (PSF) used for deconvolution. For the in situ estimation of the PSF, we developed a technique called autocorrelation scanning, in which a sample is imaged by the scanning of two excitation foci that are overlapped over various distances. The image series obtained with the variation of the distance between the two foci provides the autocorrelation function of the PSF, which can be used to estimate the PSF at specific positions within a sample. We proved the principle and the effectiveness of this technique through observations of a fluorescent biological sample, and we confirmed that the improvement in the spatial resolution was ~1.7 times that of typical two-photon excitation microscopy by observing a mouse brain phantom at a depth of 200 μm.
机译:我们提出了一种改善双光子激发显微镜的空间分辨率的技术。我们的技术将环形照明与用于解卷积的点扩展函数(PSF)的原位估计结合在一起。对于PSF的原位估计,我们开发了一种称为自相关扫描的技术,该技术通过扫描重叠在不同距离上的两个激发焦点来成像样本。随着两个焦点之间距离的变化而获得的图像序列提供了PSF的自相关函数,可用于估计样品中特定位置的PSF。我们通过观察荧光生物样本证明了该技术的原理和有效性,并且通过观察小鼠脑部幻影的深度,我们确认了空间分辨率的提高约为典型的双光子激发显微镜的1.7倍。 200微米

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