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March 3, 2026Optics Letters2 citations

Accelerated Richardson–Lucy deconvolution by unmatched projection pairs for 3D fluorescence microscopy

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HDHeheng DuNanjing University of Science and TechnologyNZNing ZhouNanjing University of Science and TechnologyHTHanci TangNanjing University of Science and Technology

Key Points

  • High-resolution 3D imaging enables significant reduction in computational cost, allowing scalability in fluorescence microscopy.
  • WB-ARL reduces iteration requirements by over 10-fold compared to conventional Richardson-Lucy deconvolution methods.
  • CUDA acceleration boosts processing speed by 40-fold, enhancing the performance of both WB-ARL and traditional methods.
  • This technique offers a scalable solution for high-throughput fluorescence microscopy, facilitating real-time volumetric visualization.

Abstract

The Richardson-Lucy deconvolution (RLD) algorithm is widely used in fluorescence microscopy to enhance image sharpness, yet its high computational complexity limits scalability for large three-dimensional (3D) datasets and impedes real-time volumetric visualization. Here, we introduce an accelerated RLD approach using a Wiener-Butterworth unmatched backprojector, termed WB-ARL, which flattens the spectral product between the forward and backprojectors while effectively suppressing high-frequency noise beyond the diffraction limit. WB-ARL reduces the number of iterations required by more than 10-fold compared with conventional RLD while maintaining high-fidelity reconstruction. CUDA acceleration further increases the speed of both methods by 40-fold while maintaining our method's iterative advantage for up to 400× increase over non-CUDA accelerated matched backprojectors. We further analyze its robustness to noise and optical aberrations and validate its performance through 3D reconstructions of both wide-field mouse kidney tissue and confocal cell phantoms. Our results demonstrate that WB-ARL enables high-resolution, high-fidelity 3D imaging with significantly reduced computational cost, offering a scalable solution for high-throughput fluorescence microscopy.

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Cite This Study

Du et al. (2026) studied this question.

synapsesocial.com/papers/69a767dbbadf0bb9e87e2a19https://doi.org/10.1364/ol.587803
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