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Confocal microscopy is a standard modality for volumetric imaging of biological samples due to its high spatial resolution and signal-to-noise ratio (SNR). However, the slow point-by-point scanning process limits its image acquisition speed. Multifocal illumination allows for faster acquisition but compromises spatial resolution. Here, we introduce a deep learning approach for multifocal confocal microscopy that achieves faster acquisition while preserving high resolution. The proposed model is based on image-to-image translation, implemented using modified U-Net, ResU-Net, and Attention U-Net architectures. The model is trained and tested on paired experimental datasets, with conventional confocal images as groundtruth and multifocal confocal images as input from various biological samples. The modified Attention U-Net significantly improves image quality and retains structural details, with higher peak SNR (32.83 dB) and structural similarity index measure (0.935) values. Additionally, spatial frequency analysis and Fourier ring correlation confirm that the Attention U-Net outperforms other models in preserving both low-frequency (>0.92 accuracy) and high-frequency information (0.90 vs. 0.83 for U-Net). Performance metrics demonstrate that our models match the quality of traditional confocal imaging, increasing imaging speed and addressing the trade-off between speed and resolution in multifocal confocal microscopy. These findings underscore the potential of combining deep learning with various confocal imaging applications.
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http://dx.doi.org/10.1364/OE.546724 | DOI Listing |
Confocal microscopy is a standard modality for volumetric imaging of biological samples due to its high spatial resolution and signal-to-noise ratio (SNR). However, the slow point-by-point scanning process limits its image acquisition speed. Multifocal illumination allows for faster acquisition but compromises spatial resolution.
View Article and Find Full Text PDFZhonghua Yan Ke Za Zhi
August 2025
Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Institute of Ophthalmology, Beijing Key Laboratory of Ophthalmology & Visual Sciences, Beijing 100730, China.
To investigate the clinical and etiological characteristics of microsporidial keratitis (MK). A retrospective case series study was conducted. Clinical data were collected from patients diagnosed with MK at Beijing Tongren Hospital, Capital Medical University between June 2023 and April 2025, including risk factors, time to diagnosis, clinical manifestations, laboratory findings, best-corrected visual acuity (BCVA) before and after treatment, and cure duration.
View Article and Find Full Text PDFLight Sci Appl
August 2025
Department of Biomedical Engineering, National Biomedical Imaging Center, College of Future Technology, Peking University, Beijing, China.
Super-resolution imaging has revolutionized our ability to visualize biological structures at subcellular scales. However, deep-tissue super-resolution imaging remains constrained by background interference, which leads to limited depth penetration and compromised imaging fidelity. To overcome these challenges, we propose a novel imaging system, confocal² spinning-disk image scanning microscopy (CSD-ISM).
View Article and Find Full Text PDFAlzheimers Res Ther
June 2025
Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Tremona Road, Southampton SO16 6YD, MP806, UK.
Background: Age-related macular degeneration (AMD) is the commonest cause of irreversible blindness in developed societies. AMD coincides with advanced age to which genetic and lifestyle factors contribute additional risks. High levels of the Alzheimer's-linked Amyloid beta (Aβ) proteins are correlated with aged/AMD retinas.
View Article and Find Full Text PDFMethods Appl Fluoresc
June 2025
College of Optical and Electronic Technology, China Jiliang University, 310000 Hangzhou, People's Republic of China.
Multifocal Structured Illumination Microscopy (MSIM) was initially introduced as a parallel version of image scanning microscopy, aiming to enhance the temporal resolution of the imaging process. Beyond its capacity in super-resolution imaging, MSIM exhibits optical sectioning capabilities akin to confocal microscopy, making it well-suited for imaging thick tissue samples. Traditional MSIM reconstruction algorithms rely on digital pinholes to eliminate out-of-focus signals, demanding precise illumination information.
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