Abstract

Spectrally encoded confocal microscopy (SECM) is a reflectance confocal microscopy technology that uses a diffraction grating to illuminate different locations on the sample with distinct wavelengths. SECM can obtain line images without any beam scanning devices, which opens up the possibility of high-speed imaging with relatively simple probe optics. This feature makes SECM a promising technology for rapid endoscopic imaging of internal organs, such as the esophagus, at microscopic resolution. SECM imaging of the esophagus has been previously demonstrated at relatively low line rates (5 kHz). In this paper, we demonstrate SECM imaging of large regions of esophageal tissues at a high line imaging rate of 100 kHz. The SECM system comprises a wavelength-swept source with a fast sweep rate (100 kHz), high output power (80 mW), and a detector unit with a large bandwidth (100 MHz). The sensitivity of the 100-kHz SECM system was measured to be 60 dB and the transverse resolution was 1.6 µm. Excised swine and human esophageal tissues were imaged with the 100-kHz SECM system at a rate of 6.6 mm(2)/sec. Architectural and cellular features of esophageal tissues could be clearly visualized in the SECM images, including papillae, glands, and nuclei. These results demonstrate that large-area SECM imaging of esophageal tissues can be successfully conducted at a high line imaging rate of 100 kHz, which will enable whole-organ SECM imaging in vivo.

Highlights

  • Confocal laser endomicroscopy (CLE) is a promising imaging technology that can provide microscopic images of the gastrointestinal (GI) organs in vivo [1]

  • Spectrally encoded confocal microscopy (SECM) imaging of the esophagus has been previously demonstrated at relatively low line rates (5 kHz)

  • We demonstrate SECM imaging of large regions of esophageal tissues at a high line imaging rate of 100 kHz

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Summary

Introduction

Confocal laser endomicroscopy (CLE) is a promising imaging technology that can provide microscopic images of the gastrointestinal (GI) organs in vivo [1]. The small FOV makes it challenging to conduct confocal imaging of the entire tissue region that may be at risk. Recent studies showed that the FOV can be increased by manually moving the CLE probe relative to the tissue and mosaicking the images together [5]. Even with these advances, CLE is only capable of imaging large luminal organs in limited focal areas. The FOV can be increased further, even to the size of the entire organ, if the imaging speed (i.e. line rate) can be increased significantly and if the CLE probe can be rapidly scanned in a controlled manner

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