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Wide-field, high-resolution Fourier ptychographic microscopy

机译:宽视场高分辨率傅里叶色谱分析

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摘要

We report an imaging method, termed Fourier ptychographic microscopy (FPM), which iteratively stitches together a number of variably illuminated, low-resolution intensity images in Fourier space to produce a wide-field, high-resolution complex sample image. By adopting a wavefront correction strategy, the FPM method can also correct for aberrations and digitally extend a microscope's depth of focus beyond the physical limitations of its optics. As a demonstration, we built a microscope prototype with a resolution of 0.78 μm, a field of view of ~120 mm 2 and a resolution-invariant depth of focus of 0.3 mm (characterized at 632 nm). Gigapixel colour images of histology slides verify successful FPM operation. The reported imaging procedure transforms the general challenge of high-throughput, high-resolution microscopy from one that is coupled to the physical limitations of the system's optics to one that is solvable through computation.
机译:我们报告了一种成像方法,称为傅里叶液相色谱(FPM),该方法将傅里叶空间中的许多可变照明的低分辨率强度图像迭代拼接在一起,以产生宽视野,高分辨率的复杂样本图像。通过采用波前校正策略,FPM方法还可以校正像差,并以数字方式将显微镜的焦深扩展到其光学器件的物理限制之外。作为演示,我们构建了一个显微镜原型,分辨率为0.78μm,视野为〜120 mm 2,分辨率不变的景深为0.3 mm(表征为632 nm)。组织学幻灯片的千兆像素彩色图像验证了FPM操作是否成功。报道的成像程序将高通量,高分辨率显微镜的一般挑战从与系统光学的物理局限性耦合的问题转变为可以通过计算解决的问题。

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