Related Experiment Video
Updated: Jun 3, 2025

An Integrated Raman Spectroscopy and Mass Spectrometry Platform to Study Single-Cell Drug Uptake, Metabolism, and Effects
Published on: January 9, 2020
Self-Supervised and Zero-Shot Learning in Multi-Modal Raman Light Sheet Microscopy
Pooja Kumari1, Johann Kern2, Matthias Raedle1
1CeMOS Research and Transfer Center, Mannheim University of Applied Sciences, 68163 Mannheim, Germany.
Abstract:
Advancements in Raman light sheet microscopy have provided a powerful, non-invasive, marker-free method for imaging complex 3D biological structures, such as cell cultures and spheroids. By combining 3D tomograms made by Rayleigh scattering, Raman scattering, and fluorescence detection, this modality captures complementary spatial and molecular data, critical for biomedical research, histology, and drug discovery. Despite its capabilities, Raman light sheet microscopy faces inherent limitations, including low signal intensity, high noise levels, and restricted spatial resolution, which impede the visualization of fine subcellular structures. Traditional enhancement techniques like Fourier transform filtering and spectral unmixing require extensive preprocessing and often introduce artifacts. More recently, deep learning techniques, which have shown great promise in enhancing image quality, face their own limitations. Specifically, conventional deep learning models require large quantities of high-quality, manually labeled training data for effective denoising and super-resolution tasks, which is challenging to obtain in multi-modal microscopy. In this study, we address these limitations by exploring advanced zero-shot and self-supervised learning approaches, such as ZS-DeconvNet, Noise2Noise, Noise2Void, Deep Image Prior (DIP), and Self2Self, which enhance image quality without the need for labeled and large datasets. This study offers a comparative evaluation of zero-shot and self-supervised learning methods, evaluating their effectiveness in denoising, resolution enhancement, and preserving biological structures in multi-modal Raman light sheet microscopic images. Our results demonstrate significant improvements in image clarity, offering a reliable solution for visualizing complex biological systems. These methods establish the way for future advancements in high-resolution imaging, with broad potential for enhancing biomedical research and discovery.
Related Concept Videos
Confocal Fluorescence Microscopy
Super-resolution Fluorescence Microscopy
Raman Spectroscopy: Overview
However, a small fraction of the scattered light exhibits a frequency shift due to the exchange of energy between the incident photons and...
Raman Spectroscopy Instrumentation: Overview
The monochromatic laser source, typically using visible or near-infrared radiation, generates a highly focused beam of light. This light interacts with the molecules of the sample, scattering some of the light. Liquid and gaseous samples are usually tested in ordinary glass capillaries, while solids can be analyzed as powders packed in capillaries or as potassium...

