Wu Jianglai, Tang Anson H L, Mok Aaron T Y, Yan Wenwei, Chan Godfrey C F, Wong Kenneth K Y, Tsia Kevin K
Department of Electrical and Electronic Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
Department of Pediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong Pokfulam Road, Hong Kong, China.
Biomed Opt Express. 2017 Aug 21;8(9):4160-4171. doi: 10.1364/BOE.8.004160. eCollection 2017 Sep 1.
Apart from the spatial resolution enhancement, scaling of temporal resolution, equivalently the imaging throughput, of fluorescence microscopy is of equal importance in advancing cell biology and clinical diagnostics. Yet, this attribute has mostly been overlooked because of the inherent speed limitation of existing imaging strategies. To address the challenge, we employ an all-optical laser-scanning mechanism, enabled by an array of reconfigurable spatiotemporally-encoded virtual sources, to demonstrate ultrafast fluorescence microscopy at line-scan rate as high as 8 MHz. We show that this technique enables high-throughput single-cell microfluidic fluorescence imaging at 75,000 cells/second and high-speed cellular 2D dynamical imaging at 3,000 frames per second, outperforming the state-of-the-art high-speed cameras and the gold-standard laser scanning strategies. Together with its wide compatibility to the existing imaging modalities, this technology could empower new forms of high-throughput and high-speed biological fluorescence microscopy that was once challenged.
除了提高空间分辨率外,在推进细胞生物学和临床诊断方面,荧光显微镜的时间分辨率缩放(等同于成像通量)同样重要。然而,由于现有成像策略固有的速度限制,这一特性大多被忽视了。为应对这一挑战,我们采用了一种全光学激光扫描机制,该机制由一系列可重构的时空编码虚拟光源实现,以展示高达8 MHz线扫描速率的超快荧光显微镜。我们表明,该技术能够以每秒75,000个细胞的速度进行高通量单细胞微流控荧光成像,并以每秒3,000帧的速度进行高速细胞二维动态成像,优于目前最先进的高速相机和金标准激光扫描策略。再加上它与现有成像模式的广泛兼容性,这项技术可以催生曾经面临挑战的新型高通量和高速生物荧光显微镜。