| Literature DB >> 28966855 |
Jianglai Wu1, Anson H L Tang1, Aaron T Y Mok1, Wenwei Yan1, Godfrey C F Chan2, Kenneth K Y Wong1, Kevin K Tsia1.
Abstract
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.Keywords: (110.0180) Microscopy; (110.2970) Image detection systems; (120.5800) Scanners; (170.0110) Imaging systems; (180.2520) Fluorescence microscopy
Year: 2017 PMID: 28966855 PMCID: PMC5611931 DOI: 10.1364/BOE.8.004160
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732