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生物组织中共聚焦显微镜的高效蒙特卡罗模拟

Efficient Monte Carlo simulation of confocal microscopy in biological tissue.

作者信息

Schmitt J M, Ben-Letaief K

机构信息

Department of Electrical and Engineering, Hong Kong University of Science and Technology, Kowloon, Hong Kong.

出版信息

J Opt Soc Am A Opt Image Sci Vis. 1996 May;13(5):952-61. doi: 10.1364/josaa.13.000952.

Abstract

A variance-reduction technique is described that greatly improves the efficacy of Monte Carlo simulations of reflection-mode confocal microscopy in anisotropically scattering media. The efficiency gain is large enough that the performance of confocal microscopes probing as deep as 5 scattering lengths can be simulated with a desktop computer. We use the technique to simulate the response of a true confocal microscope probing biological tissue, a problem that has been impractical to undertake by using conventional Monte Carlo methods. Our most important finding is that operation of a confocal microscope in the true confocal mode enables much more effective rejection of undesired scattered light than operation in the partially coherent mode, but the maximum probing depths of microscopes operated in either mode are similar (2-3) scattering lengths) in practice because of sensitivity limitations.

摘要

描述了一种方差减少技术,该技术极大地提高了在各向异性散射介质中反射模式共聚焦显微镜蒙特卡罗模拟的效率。效率提升幅度足够大,以至于使用台式计算机就能模拟探测深度达5个散射长度的共聚焦显微镜的性能。我们使用该技术模拟了一台真实共聚焦显微镜探测生物组织的响应,而这一问题用传统蒙特卡罗方法是难以解决的。我们最重要的发现是,与部分相干模式相比,真实共聚焦模式下的共聚焦显微镜能更有效地抑制不需要的散射光,但由于灵敏度限制,实际上两种模式下显微镜的最大探测深度相似(2 - 3个散射长度)。

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