Department of Neurophysiology, Brain Research Institute, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
Opt Lett. 2010 May 1;35(9):1413-5. doi: 10.1364/OL.35.001413.
Light-sheet-based fluorescence imaging techniques rely on simultaneous excitation of a single optical plane and thus permit high-contrast optically sectioned imaging of extended tissue samples. Here, we introduce a miniaturized fiber-optic implementation of a selective plane-illumination microscope (miniSPIM). The excitation light was delivered through a single-mode optical fiber, and a light-sheet was created with a cylindrical gradient-index lens and a right-angle microprism. Fluorescence emission was collected orthogonally to the light-sheet through a gradient-index lens assembly and a coherent fiber bundle. The end face of the fiber bundle was imaged onto a charge-coupled device camera. The spatial resolutions of the miniSPIM were 3.2 microm laterally and 5.1 microm axially. Images of fluorescent beads and neurons in mouse neocortex exhibited superior axial resolution and contrast in the miniSPIM-mode compared to images recorded in epi-illumination mode. The miniSPIM may thus enable novel in vivo imaging approaches.
基于光片的荧光成像技术依赖于对单个光学平面的同时激发,因此能够对扩展的组织样本进行高对比度光学切片成像。在这里,我们引入了一种微型光纤实现的选择平面照明显微镜(miniSPIM)。激发光通过单模光纤传输,通过圆柱形梯度折射率透镜和直角微棱镜创建光片。荧光发射通过梯度折射率透镜组件和相干光纤束与光片正交收集。光纤束的端面被成像到 CCD 相机上。miniSPIM 的空间分辨率为 3.2 微米侧向和 5.1 微米轴向。与在 epi-illumination 模式下记录的图像相比,在 miniSPIM 模式下,荧光珠和小鼠新皮层神经元的图像表现出更高的轴向分辨率和对比度。因此,miniSPIM 可以实现新的活体成像方法。