摄影术
显微镜
镜头(地质)
吞吐量
计算机科学
光学
傅里叶变换
成像体模
相位恢复
显微镜
校准
快速傅里叶变换
材料科学
计算机硬件
计算机视觉
算法
衍射
物理
电信
无线
量子力学
作者
Chen Liang,Feng Fan,Ke Du,Dongdong Chen,Runjia Yang,Chang Lü,Shumin Chen,Jianzhong Xi,Heng Mao
标识
DOI:10.1016/j.optlaseng.2024.108055
摘要
Label-free microscopy directly images live samples without fluorescent markers, providing a panoramic view of biological structures and functions. However, pursuing high-throughput and high-content live cell imaging requires both higher spatial resolution and larger field of view, which are limited by the optical system. In this study, we custom-built a 5/0.35 objective with a field number of 28 mm, providing a space-bandwidth product of 34 megapixels, which is four times greater than that of commercial high-throughput objectives such as the Nikon Lambda series (4/0.2, 10/0.45, 20/0.75). Furthermore, we incorporated Fourier ptychography microscopy (FPM) into the system, achieving a synthetic numerical aperture of 0.72, suitable for digital pathology and long-term live cell observation. To improve the FPM performance, we proposed a phantom-based calibration method for quantitative correction of illumination angle errors. Additionally, this method can also serve as an initial step for the on-line calibration. The remarkable capabilities of our 5/0.35 objective have been demonstrated, as well as the effectiveness of computational label-free microscopy. Furthermore, by combining our original FPM with more advanced hardware and algorithms, our FPM can achieve higher performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI