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变浸式高数值孔径显微镜。

Variable immersion microscopy with a high numerical aperture.

出版信息

Opt Lett. 2021 Feb 15;46(4):856-859. doi: 10.1364/OL.416006.

Abstract

Three-dimensional (3D) optical microscopy with a high numerical aperture (NA) remains challenging for thick biological specimens owing to aberrations arising from interface refractions. We developed a variable immersion lens (VIL) to passively minimize these aberrations. A VIL is a high-NA concentric meniscus lens and was used in combination with an aberration-corrected high-NA reflecting objective (TORA-FUJI mirror). Wave-optics simulation at a wavelength of 488 nm showed that a VIL microscope enables diffraction-limited 1.2-NA imaging in water (refractive index of 1.34) at a depth of 0.3 mm by minimizing aberrations due to refraction of a sample interface. Another aberration due to the refractive index mismatching between a mounting medium, and an object can also be corrected by the VIL system, because various fluids with different refractive indices can be used as mounting media for the VIL. As a result of correcting the two aberrations at the same time, we experimentally demonstrated that a 6 µm diameter fluorescent bead can be imaged to the true dimensions in 3D.

摘要

三维(3D)光学显微镜在对厚生物样本进行高数值孔径(NA)观察时仍具有挑战性,这是因为界面折射会产生像差。我们开发了一种可变浸液透镜(VIL)来被动地最小化这些像差。VIL 是一种高 NA 同心弯月透镜,与经过像差校正的高 NA 反射物镜(TORA-FUJI 反射镜)结合使用。在 488nm 波长下的波动光学模拟表明,VIL 显微镜通过最小化因样本界面折射而产生的像差,能够在水(折射率为 1.34)中实现 1.2-NA 的衍射极限成像,深度为 0.3mm。由于 VIL 系统可以校正由安装介质与物体之间的折射率不匹配引起的另一种像差,因此可以使用具有不同折射率的各种流体作为 VIL 的安装介质。通过同时校正这两种像差,我们在实验中证明了可以将 6μm 直径的荧光珠以其真实尺寸在 3D 中进行成像。

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