Gibson S F, Lanni F
Center for Fluorescence Research in Biomedical Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213.
J Opt Soc Am A. 1992 Jan;9(1):154-66. doi: 10.1364/josaa.9.000154.
Oil-immersion microscope objective lenses have been designed and optimized for the study of thin, two-dimensional object sections that are mounted immediately below the coverslip in a medium that is index matched to the immersion oil. It has been demonstrated both experimentally and through geometrical- and physical-optics theory that, when the microscope is not used with the correct coverslip or immersion oil, when the detector is not located at the optimal plane in image space, or when the object does not satisfy specific conditions, aberration will degrade both the contrast and the resolution of the image. In biology the most severe aberration is introduced when an oil-immersion objective lens is used to study thick specimens, such as living cells and tissues, whose refractive indices are significantly different from that of the immersion oil. We present a model of the three-dimensional imaging properties of a fluorescence light microscope subject to such aberration and compare the imaging properties predicted by the model with those measured experimentally. The model can be used to understand and compensate for aberration introduced to a microscope system under nondesign optical conditions so that both confocal laser scanning microscopy and optical serial sectioning microscopy can be optimized.
油浸显微镜物镜是为研究薄的二维物体切片而设计和优化的,这些切片安装在盖玻片正下方的一种与浸油折射率匹配的介质中。实验以及几何光学和物理光学理论均已证明,当显微镜未使用正确的盖玻片或浸油时,当探测器未位于像空间中的最佳平面时,或者当物体不满足特定条件时,像差会降低图像的对比度和分辨率。在生物学中,当使用油浸物镜研究厚标本(如活细胞和组织,其折射率与浸油的折射率有显著差异)时,会引入最严重的像差。我们提出了一个受此类像差影响的荧光显微镜三维成像特性模型,并将该模型预测的成像特性与实验测量的成像特性进行比较。该模型可用于理解和补偿在非设计光学条件下引入显微镜系统的像差,从而优化共聚焦激光扫描显微镜和光学连续切片显微镜。