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Updated: Oct 28, 2026

Excitation-Scanning Hyperspectral Imaging Microscopy to Efficiently Discriminate Fluorescence Signals
Published on: August 22, 2019
SuperEEM: A Super-Resolution Reconstruction Framework for Rapid and Reliable Excitation-Emission Matrix Fluorescence
Jun Zeng1, Bao-Shuo Jia1,2, Yao Chen1,3
1State Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, Hunan University, Changsha410082, PR China.
Abstract:
Excitation-emission matrix (EEM) fluorescence spectroscopy is widely used for characterizing complex samples in food analysis and environmental monitoring, but its practical deployment is limited by the trade-off between spectral resolution and acquisition speed. High-resolution EEM acquisition is time-consuming, whereas rapid low-resolution measurements lose analytically important spectral details. Herein, we introduce SuperEEM, a chemically constrained super-resolution framework for converting rapidly acquired sparse EEMs into analytically reliable high-resolution EEMs. Unlike generic image super-resolution approaches that mainly optimize visual similarity, SuperEEM couples an EEM-tailored U-Net-GAN architecture with a quantitative-fidelity-oriented loss function to preserve fluorescence intensity, peak topology, and excitation-emission relationships. The analytical reliability of SuperEEM was validated using three representative tasks: polycyclic aromatic hydrocarbon (PAH) quantification, edible oil classification, and beer classification. Compared with LR EEMs, SuperEEM-reconstructed EEMs substantially improved downstream performance, achieving PAH quantification comparable to original HR EEMs and improving classification accuracy from 77.4% to 90.3% for edible oils and from 73.3% to 86.7% for beers. Under the tested instrumental settings, SuperEEM enabled a 14-fold improvement in EEM acquisition efficiency while maintaining analytical reliability. A graphical user interface (GUI) was further developed to support model application, visualization, and result export. These results demonstrate the potential of SuperEEM for rapid, high-throughput fluorescence analysis.

