Shaked Natan T, Newpher Thomas M, Ehlers Michael D, Wax Adam
1Department of Biomedical Engineering, Fitzpatrick Institute for Photonics, Duke University,Durham, North Carolina 27708, USA.
Appl Opt. 2010 May 20;49(15):2872-8. doi: 10.1364/AO.49.002872.
We apply a wide-field quantitative phase microscopy technique based on parallel two-step phase-shifting on-axis interferometry to visualize live biological cells and microorganism dynamics. The parallel on-axis holographic approach is more efficient with camera spatial bandwidth consumption compared to previous off-axis approaches and thus can capture finer sample spatial details, given a limited spatial bandwidth of a specific digital camera. Additionally, due to the parallel acquisition mechanism, the approach is suitable for visualizing rapid dynamic processes, permitting an interferometric acquisition rate equal to the camera frame rate. The method is demonstrated experimentally through phase microscopy of neurons and unicellular microorganisms.
我们应用一种基于并行两步相移同轴干涉测量法的宽场定量相显微镜技术来可视化活体细胞和微生物的动态。与之前的离轴方法相比,并行同轴全息方法在相机空间带宽消耗方面更高效,因此在特定数码相机空间带宽有限的情况下能够捕捉到更精细的样本空间细节。此外,由于并行采集机制,该方法适用于可视化快速动态过程,允许干涉测量采集速率等于相机帧率。通过对神经元和单细胞微生物进行相显微镜实验验证了该方法。