FPM-WSI: Fourier ptychographic whole slide imaging via feature-domain backdiffraction

被引:8
|
作者
Zhang, Shuhe [1 ,2 ,3 ]
Wang, Aiye [1 ,4 ]
Xu, Jinghao [1 ,4 ]
Feng, Tianci [1 ,4 ]
Zhou, Jinhua [3 ]
Pan, An [1 ,4 ]
机构
[1] Chinese Acad Sci, State Key Lab Transient Opt & Photon, Xian Inst Opt & Precis Mech, Xian 710119, Peoples R China
[2] Maastricht Univ, Med Ctr, NL-6202 AZ Maastricht, Netherlands
[3] Anhui Med Univ, Sch Biomed Engn, Hefei 230032, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
来源
OPTICA | 2024年 / 11卷 / 05期
基金
中国国家自然科学基金;
关键词
MISALIGNMENT CORRECTION METHOD; PHASE RETRIEVAL; WIDE-FIELD; MICROSCOPY; ILLUMINATION; ROBUSTNESS;
D O I
10.1364/OPTICA.517277
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Fourier ptychographic microscopy (FPM) theoretically provides a solution to the trade-off between spatial resolution and field of view (FOV), and has promising prospects in digital pathology. However, block reconstruction and then stitching has become an unavoidable procedure for reconstruction of large FOV due to vignetting artifacts. This introduces digital stitching artifacts, as the existing image-domain optimization algorithms are highly sensitive to systematic errors. Such obstacles significantly impede the advancement and practical implementation of FPM, explaining why, despite a decade of development, FPM has not gained widespread recognition in the field of biomedicine. We report a feature-domain FPM (FD-FPM) based on the structure-aware forward model to realize stitching-free, full-FOV reconstruction. The loss function is uniquely formulated in the feature domain of images, which bypasses the troublesome vignetting effect and algorithmic vulnerability via feature-domain backdiffraction. Through massive simulations and experiments, we show that FD-FPM effectively eliminates vignetting artifacts for full-FOV reconstruction, and still achieves impressive reconstructions despite the presence of various systematic errors. We also found it has great potential in recovering the data with a lower spectrum overlapping rate, and in realizing digital refocusing without a prior defocus distance. With FD-FPM, we achieved full-color and high-throughput imaging (4.7 mm diameter FOV, 336 nm resolution in the blue channel) free of blocking-and-stitching procedures on a self-developed Fourier ptychographic microscopy whole slide imaging platform. The reported FD-FPM shows the value of FPM for various experimental circumstances, and offers physical insights useful for the developments of models for other computational imaging techniques. The reported platform demonstrates high-quality, high -speed imaging and low cost, and could find applications in many fields of biomedical research, as well as in clinical applications. (c) 2024 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement
引用
收藏
页码:634 / 646
页数:13
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