Self-calibrated 3D differential phase contrast microscopy with optimized illumination

被引:12
作者
Cao, Ruiming [1 ]
Kellman, Michael [2 ]
Ren, David [2 ]
Eckert, Regina [2 ]
Waller, Laura [2 ]
机构
[1] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Elect Engn & Comp Sci, Berkeley, CA 94720 USA
基金
美国国家科学基金会;
关键词
HIGH-RESOLUTION; DIFFRACTION TOMOGRAPHY; HIGH-THROUGHPUT; INTENSITY; FIELD; DEPTH;
D O I
10.1364/BOE.450838
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
3D phase imaging recovers an object's volumetric refractive index from intensity and/or holographic measurements. Partially coherent methods, such as illumination-based differential phase contrast (DPC), are particularly simple to implement in a commercial brightfield microscope. 3D DPC acquires images at multiple focus positions and with different illumination source patterns in order to reconstruct 3D refractive index. Here, we present a practical extension of the 3D DPC method that does not require a precise motion stage for scanning the focus and uses optimized illumination patterns for improved performance. The user scans the focus by hand, using the microscope's focus knob, and the algorithm self-calibrates the axial position to solve for the 3D refractive index of the sample through a computational inverse problem. We further show that the illumination patterns can be optimized by an end-to-end learning procedure. Combining these two, we demonstrate improved 3D DPC with a commercial microscope whose only hardware modification is LED array illumination. (c) 2022 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement
引用
收藏
页码:1671 / 1684
页数:14
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