The capability to perform multicolor, wide field-of-view (FOV) fluorescence microscopy imaging is important in screening and pathology applications. We developed a microscopic slide-imaging system that can achieve multicolor, wide FOV, fluorescence imaging based on the Talbot effect. In this system, a light-spot grid generated by the Talbot effect illuminates the sample. By tilting the excitation beam, the Talbot-focused spot scans across the sample. The images are reconstructed by collecting the fluorescence emissions that correspond to each focused spot with a relay optics arrangement. The prototype system achieved an FOV of 12 × 10 mm^2 at an acquisition time as fast as 23 s for one fluorescence channel. The resolution is fundamentally limited by spot size, with a demonstrated full-width at half-maximum spot diameter of 1.2 μm. The prototype was used to nimage green fluorescent beads, double-stained human breast cancer SK-BR-3 cells, Giardia lamblia cysts, and the Cryptosporidium parvum oocysts. This imaging method is scalable and simple for implementation of high-speed wide FOV fluorescence microscopy.
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机译:执行多色,宽视场(FOV)荧光显微镜成像的功能在筛查和病理学应用中很重要。我们开发了一种显微幻灯片成像系统,可以基于Talbot效应实现多色,宽视场,荧光成像。在该系统中,由塔尔伯特效应产生的光斑栅格照亮了样品。通过倾斜激发光束,聚焦于Talbot的点扫描样品。通过使用中继光学装置收集与每个聚焦点相对应的荧光发射来重建图像。该原型系统在一个荧光通道的采集时间高达23 s时实现了FOV为12×10 mm ^ 2。分辨率从根本上受到光斑尺寸的限制,在最大光斑直径的一半处显示的全宽为1.2μm。该原型用于对绿色荧光珠,双重染色的人乳腺癌SK-BR-3细胞,贾第鞭毛虫囊肿和隐孢子虫卵囊进行染色。这种成像方法可扩展且易于实现高速宽视场荧光显微镜。
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