Abstract

Reflectance confocal microscopy (RCM) is a non-invasive high-resolution optical imaging technique used in clinical settings as a diagnostic method. However, RCM has limited diagnostic ability by providing non-specific morphological information only based on reflection contrast. Various multimodal imaging techniques have been developed to compensate the limitations of RCM, but multimodal techniques are often slow in imaging speed compared to RCM alone. In this report, we combined RCM with moxifloxacin based two-photon microscopy (TPM) for high-speed multimodal imaging. Moxifloxacin based TPM used clinically compatible moxifloxacin for cell labeling and could do non-invasive cellular imaging at 30 frames/s together with RCM. Performance of the combined microscopy was characterized in the imaging of mouse skin and cornea, in vivo. Detail tissue microstructures including cells, extra-cellular matrix (ECM), and vasculature were visualized. The combined microscopy was applied to human skin cancer specimens, and both cells and ECM in the skin cancer and normal skin regions were visualized at high imaging speeds. The combined microscopy can be useful in the clinical applications of RCM by providing multiple contrasts.

Highlights

  • Reflectance confocal microscopy (RCM) is a 3D imaging technique based on light reflection from samples

  • We developed a combined reflectance confocal (RC) and moxifloxacin based twophoton (TP) microscopy for multi-contrast high-speed tissue imaging

  • Dermal cells and collagen were shown in the two-photon fluorescence (TPF)/second harmonic generation (SHG) channel and fibrous extra-cellular matrix (ECM) structures and vessels were shown in the RC channel (Fig. 2(c, d)) Scattered cells in the dermis were shown in the TPF channel with moxifloxacin labeling, while they were not visible in the RC channel

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Summary

Introduction

Reflectance confocal microscopy (RCM) is a 3D imaging technique based on light reflection from samples. RCM has been used as a diagnostic method in clinical settings by providing high-resolution cellular images non-invasively [1,2,3,4,5,6,7]. RCM has been used for non-invasive detection of infecting pathogens in the diagnosis of corneal keratitis and other ocular surface complications [6,7]. RCM has limitations in the clinical applications by providing morphological information based on reflection contrast. Even if reflection contrast provides clear visualization, morphological information from RCM may not be specific to detect cells of interest or infecting pathogens.

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