Abstract

In this paper, excitation light wavefront modulation is performed considering the curved sample surface shape to demonstrate high-quality deep observation using two-photon excitation microscopy (TPM) with a dry objective lens. A large spherical aberration typically occurs when the refractive index (RI) interface between air and the sample is a plane perpendicular to the optical axis. Moreover, the curved sample surface shape and the RI mismatch cause various aberrations, including spherical ones. Consequently, the fluorescence intensity and resolution of the obtained image are degraded in the deep regions. To improve them, we designed a pre-distortion wavefront for correcting the aberration caused by the curved sample surface shape by using a novel, simple optical path length difference calculation method. The excitation light wavefront is modulated to the pre-distortion wavefront by a spatial light modulator incorporated in the TPM system before passing through the interface, where the RI mismatch occurs. Thus, the excitation light is condensed without aberrations. Blood vessels were thereby observed up to an optical depth of 2,000 μm in a cleared mouse brain by using a dry objective lens.

Highlights

  • The observation of a given biological sample with cellular-level resolution is expected to be performed for the investigation of biological functions

  • An additional effective approach involves pressing a glass-bottom dish on the sample so that the interface between air and the sample becomes perpendicular to the optical axis and spherical aberration becomes dominant

  • When a highly viscous immersion fluid is used for tissue clearing, large aberrations may be generated owing to the non-uniformity of the refractive index (RI) distribution (Schlieren phenomena) and bubbles introduced in the fluid

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Summary

Introduction

The observation of a given biological sample with cellular-level resolution is expected to be performed for the investigation of biological functions. Various methods for reducing the effects of scattering, absorption, and aberration were proposed for observing deeper regions of biological samples. By introducing a clearing technique[16,17,18,19,20] in an in vitro experiment, scattering, absorption, and aberration were reduced, and observation at a depth of 6 mm or more was realised with a special objective lens for cleared samples[18]. When a dry objective lens is used, the curved surface shape and large RI mismatch between air and the sample strongly generate lower-order aberrations of tilt, defocus, astigmatism, coma, and spherical aberrations. To reduce the influence of the RI mismatch, an immersion-fluid objective lens is www.nature.com/scientificreports/. Even in the case of observation with an immersion-fluid objective lens, aberrations occur when observing the deep regions if any RI difference exists between the immersion fluid and the sample

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