Optical Tomography by Confocal Fluorescence Microscope

O. Nakamura, S. Kawata, S. Minami
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Abstract

In the past few years, microscope tomography has been intensively studied.1-5 Agard and Sedat restored the 3-D structure of biological cells from the focus series images given by a conventional epi-fluorescence microscope, by inverting the 3-D optical transfer function of the system.1 However, since the 3-D OTF of an epi-fluorescence microscope is angularly band-limited,6 the 3-D spatial frequency components only within the angular band can be restored in their method. As a result, the longitudinal resolution in the restored 3-D structure is not at all satisfactory.
共聚焦荧光显微镜的光学层析成像
在过去的几年里,显微镜断层扫描得到了广泛的研究。1-5 Agard和Sedat通过反转系统的三维光学传递函数,从传统的外显荧光显微镜给出的聚焦序列图像中恢复了生物细胞的三维结构然而,由于外延荧光显微镜的三维OTF是角波段限制的,因此他们的方法只能恢复角波段内的三维空间频率分量。结果表明,修复后的三维结构的纵向分辨率并不令人满意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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