Tinning Peter W, Scrimgeour Ross, McConnell Gail
Department of Physics, SUPA, University of Strathclyde, Glasgow, G4 ONG, UK.
Biomed Opt Express. 2018 Mar 16;9(4):1745-1761. doi: 10.1364/BOE.9.001745. eCollection 2018 Apr 1.
We report the first demonstration of widefield standing wave (SW) microscopy of fluorescently labelled red blood cells at high speeds that allow for the rapid imaging of membrane deformations. Using existing and custom MATLAB functions, we also present a method to generate 2D and 3D reconstructions of the SW data for improved visualization of the cell. We compare our technique with standard widefield epifluorescence imaging and show that the SW technique not only reveals more topographical information about the specimen but does so without increasing toxicity or the rate of photobleaching and could make this a powerful technique for the diagnosis or study of red blood cell morphology and biomechanical characteristics.
我们首次展示了高速宽场驻波(SW)显微镜对荧光标记红细胞的成像,该成像能够快速捕捉膜变形情况。利用现有的和自定义的MATLAB函数,我们还提出了一种生成SW数据的二维和三维重建方法,以更好地可视化细胞。我们将我们的技术与标准宽场落射荧光成像进行了比较,结果表明,SW技术不仅能揭示更多关于样本的地形信息,而且不会增加毒性或光漂白速率,这可能使其成为诊断或研究红细胞形态和生物力学特性的强大技术。