Three-photon light-sheet fluorescence microscopy

被引:40
|
作者
Escobet-Montalban, Adria [1 ]
Gasparoli, Federico M. [1 ]
Nylk, Jonathan [1 ]
Liu, Pengfei [1 ]
Yang, Zhengyi [1 ,2 ]
Dholakia, Kishan [1 ]
机构
[1] Univ St Andrews, Sch Phys & Astron, Scottish Univ Phys Alliance, North Haugh KY16 9SS, Fife, Scotland
[2] Diamond Light Source, Electron Bioimaging Ctr, Harwell Sci & Innovat Campus, Didcot OX11 0DE, Oxon, England
基金
英国工程与自然科学研究理事会; 欧盟地平线“2020”;
关键词
DEEP; EMBRYOS;
D O I
10.1364/OL.43.005484
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We present the first demonstration of three-photon excitation light-sheet fluorescence microscopy. Light-sheet fluorescence microscopy in single- and two-photon modes has emerged as a powerful wide-field, low-photodamage technique for Fast volumetric imaging of biological samples. We extend this imaging modality to the three-photon regime, enhancing its penetration depth. Our present study uses a conventional femtosecond pulsed laser at 1000 nm wavelength for the imaging of 450 mu m diameter cellular spheroids. In addition, we show, experimentally and through numerical simulations, the potential advantages in three-photon light-sheet microscopy of using propagation-invariant Bessel beams in preference to Gaussian beams. (C) 2018 Optical Society of America
引用
收藏
页码:5484 / 5487
页数:4
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