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利用选择面照明显微镜进行散射介质的深度成像。

Deep imaging in scattering media with selective plane illumination microscopy.

机构信息

Rice University, Department of Electrical and Computer Engineering, 6100 Main Street, Houston, Texas 77005, United States.

The University of Texas Health Science Center at Houston, McGovern Medical School, 6431 Fannin Street, Houston, Texas 77030, United States.

出版信息

J Biomed Opt. 2016 Dec 1;21(12):126009. doi: 10.1117/1.JBO.21.12.126009.

Abstract

In most biological tissues, light scattering due to small differences in refractive index limits the depth of optical imaging systems. Two-photon microscopy (2PM), which significantly reduces the scattering of the excitation light, has emerged as the most common method to image deep within scattering biological tissue. This technique, however, requires high-power pulsed lasers that are both expensive and difficult to integrate into compact portable systems. Using a combination of theoretical and experimental techniques, we show that if the excitation path length can be minimized, selective plane illumination microscopy (SPIM) can image nearly as deep as 2PM without the need for a high-powered pulsed laser. Compared to other single-photon imaging techniques like epifluorescence and confocal microscopy, SPIM can image more than twice as deep in scattering media ( ? 10 times the mean scattering length). These results suggest that SPIM has the potential to provide deep imaging in scattering media in situations in which 2PM systems would be too large or costly.

摘要

在大多数生物组织中,由于折射率微小差异导致的光散射限制了光学成像系统的深度。双光子显微镜(2PM)显著减少了激发光的散射,已成为在散射生物组织内部深处进行成像的最常用方法。然而,这种技术需要高功率脉冲激光器,这些激光器既昂贵又难以集成到紧凑的便携式系统中。我们结合理论和实验技术表明,如果可以最小化激发路径长度,则选择性平面照明显微镜(SPIM)可以在不需要高功率脉冲激光器的情况下实现与 2PM 相当的深层成像。与其他单光子成像技术(如荧光和共聚焦显微镜)相比,SPIM 可以在散射介质中成像深度超过两倍(比平均散射长度大 10 倍)。这些结果表明,在 2PM 系统过大或成本过高的情况下,SPIM 有可能在散射介质中提供深层成像。

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