Parallel Fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 Eyes)

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作者
Antony C. S. Chan
Jinho Kim
An Pan
Han Xu
Dana Nojima
Christopher Hale
Songli Wang
Changhuei Yang
机构
[1] California Institute of Technology,Division of Engineering & Applied Science
[2] Chinese Academy of Sciences,State Key Laboratory of Transient Optics and Photonics, Xi’an Institute of Optics and Precision Mechanics
[3] Amgen South San Francisco,undefined
[4] Samsung Engineering,undefined
[5] A2 Biotherapeutics,undefined
[6] Merck,undefined
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We report the implementation of a parallel microscopy system (96 Eyes) that is capable of simultaneous imaging of all wells on a 96-well plate. The optical system consists of 96 microscopy units, where each unit is made out of a four element objective, made through a molded injection process, and a low cost CMOS camera chip. By illuminating the sample with angle varying light and applying Fourier Ptychography, we can improve the effective brightfield imaging numerical aperture of the objectives from 0.23 to 0.3, and extend the depth of field from ±5 μm to ±15 μm. The use of Fourier Ptychography additionally allows us to computationally correct the objectives’ aberrations out of the rendered images, and provides us with the ability to render phase images. The 96 Eyes acquires raw data at a rate of 0.7 frame per second (all wells) and the data are processed with 4 cores of graphical processing units (GPUs; GK210, Nvidia Tesla K80, USA). The system is also capable of fluorescence imaging (excitation = 465 nm, emission = 510 nm) at the native resolution of the objectives. We demonstrate the capability of this system by imaging S1P1-eGFP-Human bone osteosarcoma epithelial (U2OS) cells.
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