Improving longitudinal resolution of Airy beams two-photon volume imaging with fluorescence lifetime imaging

被引:0
|
作者
Guo, Yong [1 ]
Wang, Luwei [1 ]
Zhu, Yinru [1 ]
Gao, Xinwei [1 ]
Weng, Xiaoyu [1 ]
Liu, Jinyuan [1 ]
Yan, Wei [1 ]
Qu, Junle [1 ]
机构
[1] Shenzhen Univ, Minist Educ & Guangdong Prov, Shenzhen Key Lab Photon & Biophoton, Key Lab Optoelect Devices & Syst,Coll Phys & Optoe, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
Airy volumetric image; Indistinguishable; FLIM; Phasor plot analysis approach; LIGHT-SHEET MICROSCOPY; PHASOR APPROACH; DEPTH; CELLS; PLOT;
D O I
10.1016/j.optcom.2022.129151
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The non-diffracting Airy beams have been reported to increase acquisition speed by projecting the axially significantly elongated information to a two-dimensional (2D) image. Due to the elongated focal length, an Airy volumetric image can cover information as much as stack images with multiple Gaussian images at different imaging depths, which significantly increases the volumetric imaging rate. However, the projection of three-dimensional (3D) structures on a 2D plane is usually indistinguishable, especially those that overlap along the axis. Therefore, we proposed an axially resolved volume imaging technique based on a two-photon fluorescence lifetime microscopy imaging (FLIM) by using Airy beams.
引用
收藏
页数:6
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