Paper

Virtual H&E Histology by Fiber-Based Picosecond Two-Photon Microscopy

Eibl, Matthias, Limpert, Jens, Huber, Robert, Draxinger, Wolfgang, Bringruber, Reginald, Kolb, Jan Philip, Meyer, Tobias, Gottschall, Thomas, Popp, Jürgen, Brinkmann, Ralf, Sebastian Nino Karpf, Weng, Daniel, Hakert, Hubertus

2020

Overview

Two-Photon Microscopy (TPM) can provide three-dimensional morphological and functional contrast in vivo. Through proper staining, TPM can be utilized to create virtual, H&E equivalent images and thus can improve throughput in histology-based applications. We previously reported on a new light source for TPM that employs a compact and robust fiber-amplified, directly modulated laser. This laser is pulse-to-pulse wavelength switchable between 1064 nm, 1122 nm, and 1186 nm with an adjustable pulse duration from 50ps to 5ns and arbitrary repetition rates up to 1MHz at kW-peak powers. Despite the longer pulse duration, it can achieve similar average signal levels compared to fs-setups by lowering the repetition rate to achieve similar cw and peak power levels. The longer pulses lead to a larger number of photons per pulse, which yields single shot fluorescence lifetime measurements (FLIM) by applying a fast 4 GSamples/s digitizer. In the previous setup, the wavelengths were limited to 1064 nm and longer. Here, we use four wave mixing in a non-linear photonic crystal fiber to expand the wavelength range down to 940 nm. This wavelength is highly suitable for imaging green fluorescent proteins in neurosciences and stains such as acridine orange (AO), eosin yellow (EY) and sulforhodamine 101 (SR101) used for histology applications. In a more compact setup, we also show virtual H&E histological imaging using a direct 1030 nm fiber MOPA.

• Publisher: Cornell University Library, arXiv.org
• Subject: Crystal fibers / Fluorescence / Four-wave mixing / Histology / Light sources / Microscopy / Photonic crystals / Photons / Pulse duration / Repetition