Cang Hu, Xu C Shan, Montiel Daniel, Yang Haw
Department of Chemistry, University of California at Berkeley, and Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
Opt Lett. 2007 Sep 15;32(18):2729-31. doi: 10.1364/ol.32.002729.
Confocal optical microscopes offer unparalleled high sensitivity and three-dimensional (3D) imaging capability but require slow point-by-point scanning; they are inefficient for imaging moving objects. We propose a more efficient solution. Instead of indiscriminate scanning, we let the focus of the microscope pursue the object of interest such that no time is wasted on uninformative background, allowing us to visualize 3D trajectories of fluorescent nanoparticles in solution with millisecond temporal and ~200 nm spatial resolution.
共焦光学显微镜具有无与伦比的高灵敏度和三维(3D)成像能力,但需要逐点缓慢扫描;它们对移动物体成像效率较低。我们提出了一种更有效的解决方案。我们不是进行无差别扫描,而是让显微镜的焦点追踪感兴趣的物体,这样就不会在无信息的背景上浪费时间,从而使我们能够以毫秒级的时间分辨率和约200纳米的空间分辨率可视化溶液中荧光纳米颗粒的3D轨迹。