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Improvement of axial excitation confinement in temporal focusing-based multiphoton microscopy via spatially modulated illumination

机译:通过空间调制照明改善基于时间聚焦的多光子显微镜中轴向激发的限制

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Conventional temporal focusing-based multiphoton excitation microscopy (TFMPEM) can offer widefield optical sectioning with an axial excitation confinement (AEC) of a few microns. Herein, a developed TFMPEM with a digital micromirror device (DMD), acting as the blazed grating for light spatial dispersion and simultaneous patterned illumination, has been extended to implement spatially modulated illumination at structured frequency and orientation. By implementing the spatially modulated illumination, the beam coverage at the back-focal aperture of the objective lens can be increased. As a result, the AEC can be condensed from 3.0 um to 1.5 um in full width at half maximum for a 2-fold enhancement. Furthermore, by using HiLo microscopy with two structured illuminations at the same spatial frequency but different orientation, biotissue images according to the structured illumination with condensed AEC is obviously superior in contrast and scattering suppression.
机译:常规的基于时间聚焦的多光子激发显微镜(TFMPEM)可以提供具有几微米的轴向激发限制(AEC)的宽视场光学切片。在此,具有数字微镜器件(DMD)的开发的TFMPEM,已被扩展为用于光空间色散和同时图案照明的闪耀光栅,已被扩展以实现结构化频率和方向的空间调制照明。通过实施空间调制照明,可以增加在物镜的后焦孔处的光束覆盖范围。结果,可以将AEC的全宽度从3.0 um压缩到1.5 um,最大值为一半,以实现2倍增强。此外,通过使用具有相同空间频率但方向不同的两个结构化照明的HiLo显微镜,根据结构化照明与浓缩AEC的生物组织图像在对比度和散射抑制方面显然要优越。

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