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Tomographic phase microscopy with 180 degrees rotation of live cells in suspension by holographic optical tweezers

机译:全息光学镊子在悬浮液中将活细胞旋转180度的层析相显微镜

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We present a new tomographic phase microscopy (TPM) approach that allows capturing the three-dimensional refractive index structure of single cells in suspension without labeling, using 180 degrees rotation of the cells. This is obtained by integrating an external off-axis interferometer for wide-field wave front acquisition with holographic optical tweezers (HOTs) for trapping and micro-rotation of the suspended cells. In contrast to existing TPM approaches for cell imaging, our approach does not require anchoring the sample to a rotating stage, nor is it limited in angular range as is the illumination rotation approach. Thus, it allows noninvasive TPM of suspended live cells in a wide angular range. The proposed technique is experimentally demonstrated by capturing the three-dimensional refractive index map of yeast cells, while collecting interferometric projections at an angular range of 180 degrees with 5 degrees steps. The interferometric projections are processed by both the filtered back-projection method and the diffraction theory method. The experimental system is integrated with a spinning disk confocal fluorescent microscope for validation of the label-free TPM results. (C) 2015 Optical Society of America
机译:我们提出了一种新的层析相显微镜(TPM)方法,该方法允许使用180度旋转的细胞捕获悬浮液中单个细胞的三维折射率结构而无需标记。这是通过将用于宽场波前采集的外部离轴干涉仪与用于捕获和悬浮悬浮细胞的全息光镊子(HOT)集成在一起而获得的。与用于细胞成像的现有TPM方法相反,我们的方法不需要将样品固定到旋转台上,也不需要像照明旋转方法那样在角度范围内受到限制。因此,它允许在宽角度范围内对悬浮的活细胞进行无创TPM。通过捕获酵母细胞的三维折射率图,同时以5度的步长在180度的角度范围内收集干涉投影,可以通过实验证明所提出的技术。干涉投影通过滤波反投影方法和衍射理论方法进行处理。实验系统与旋转盘共聚焦荧光显微镜集成在一起,用于验证无标记TPM结果。 (C)2015年美国眼镜学会

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