Pang Shuo, Han Chao, Erath Jessey, Rodriguez Ana, Yang Changhuei
Department of Electrical Engineering, California Institute of Technology, 1200 E. California Blvd. Pasadena, CA 91125, USA.
Opt Express. 2013 Jun 17;21(12):14555-65. doi: 10.1364/OE.21.014555.
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.
具备进行多色、宽视场(FOV)荧光显微镜成像的能力在筛选和病理学应用中至关重要。我们开发了一种基于塔尔博特效应的可实现多色、宽视场荧光成像的显微载玻片成像系统。在该系统中,由塔尔博特效应产生的光斑网格照亮样品。通过倾斜激发光束,塔尔博特聚焦光斑扫描样品。通过使用中继光学装置收集与每个聚焦光斑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最快为23秒时,实现了12×10毫米²的视场。分辨率从根本上受光斑尺寸限制,已证明半高宽光斑直径为1.2微米。该原型用于对绿色荧光珠、双色染色的人乳腺癌SK - BR - 3细胞、贾第虫囊肿和微小隐孢子虫卵囊进行成像。这种成像方法对于高速宽视场荧光显微镜的实现具有可扩展性且易于实施。