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基于电动可调焦透镜的大范围快速光片显微成像
引用本文:胡渝曜,梁东,王晶,刘军. 基于电动可调焦透镜的大范围快速光片显微成像[J]. 物理学报, 2020, 0(8): 217-225
作者姓名:胡渝曜  梁东  王晶  刘军
作者单位:中国科学院上海光学精密机械研究所;中国科学院大学
基金项目:国家自然科学基金(批准号:61527821,61521093,11804350);上海扬帆计划(批准号:17YF1421300)资助的课题.
摘    要:搭建了一种基于电动可调焦透镜(electrically tunable lens)的大范围快速光片荧光显微成像系统.通过引入电动可调焦透镜与一维振镜以实现成像物平面和光片位置的快速移动,再结合高速s CMOS完成快速光片荧光显微成像.另外实验中通过改善光路与提升动态成像质量,实现了大范围扫描并减少了伪像.最终对成像性能进行测试,本系统的纵向分辨率和横向分辨率分别达到约5.5μm和约0.7μm,单幅图像稳定成像的速度约为275 frames/s,成像深度可超过138μm,能满足对具有一定尺寸的生物样本进行实时清晰成像的需求.

关 键 词:光片荧光显微成像  电动可调焦透镜  快速成像

High-speed and large-scaled light-sheet microscopy with electrically tunable lens
Hu Yu-Yao,Liang Dong,Wang Jing,Liu Jun. High-speed and large-scaled light-sheet microscopy with electrically tunable lens[J]. Acta Physica Sinica, 2020, 0(8): 217-225
Authors:Hu Yu-Yao  Liang Dong  Wang Jing  Liu Jun
Affiliation:(State Key Laboratory of High Field Laser Physics,Shanghai Institute of Optics and Fine Mechanics,Chinese Academy of Sciences,Shanghai 201800,China;University of Chinese Academy of Sciences,Beijing 100049,China)
Abstract:Fluorescence microscopic imaging technology realizes specific imaging by labeling biological tissue with fluorescence molecules,which has a high signal-to-noise ratio and has been widely used in the field of medical biology research.Some typical fluorescence microscopy techniques,such as confocal microscopy and two-photon microscopy,have high fluorescence intensity,but the long exposure can cause phototoxicity and photobleaching of biological tissue,which is difficult to meet the demand for long-time observation or noninvasive imaging.Then,light sheet fluorescence microscopy(LSFM)has become a hot research topic in fluorescence microimaging in recent years due to its fast speed,high resolution,low photobleaching and low phototoxicity.The imaging speed of a typical light sheet microscopy is not fast enough to observe fast biological activities such as transmission of neural signals,blood flow,and heart beats.At present,many reported light-sheet fluorescence microscopies still have some problems such as fixed imaging surface,slow imaging speed,small imaging depth or residual artifacts.Therefore,in this paper,a rapid light-sheet fluorescence microscopy based on electrically tunable lens is built.To achieve the rapid movement of the focal plane of the detection objective lens,the electrically tunable lens is introduced to meet the reqirement for fast changing of the diopter.Similarly,the rapid movement of light sheet is achieved by introducing one-dimensional galvanometer to change the rotation angle.Fast imaging requires the light sheet and focal plane to overlap in real time,which is then combined with a high-speed sCMOS receiving fluorescence to complete the whole imaging.In the experiment,the vertical depth significantly increases by modifying the optical path,and the LABVIEW programming is used to coordinate and improve the dynamic imaging quality,which effectively reduces the artifacts generated in rapid imaging.Finally,an imaging speed of 275 frames/s with a lateral resolution of^0.73μm,vertical resolution of^5.5μm,and an imaging depth of^138μm is achieved.This is of significance for developing the real-time and non-invasive imaging of living biological tissues.
Keywords:light-sheet fluorescence microscopy  electrically tunable lens  fast imaging
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