Fluorescence time-resolved macroimaging

被引:35
|
作者
Shcheslavskiy, Vladislav, I [1 ,2 ]
Shirmanova, Marina, V [2 ]
Dudenkova, Varvara V. [2 ]
Lukyanov, Konstantin A. [2 ,3 ]
Gavrina, Alena, I [2 ]
Shumilova, Anastasia, V [2 ]
Zagaynova, Elena [2 ]
Becker, Wolfgang [1 ]
机构
[1] Becker & Hickl GmbH, Nahmitzer Damm 30, D-12277 Berlin, Germany
[2] Privolzhsky Res Med Univ, Inst Biomed Technol, Minin & Pozharsky Sq 10-1, Nizhnii Novgorod 603005, Russia
[3] Shemyakin Ovchinnikov Inst Bioorgan Chem, Miklukho Maklaya St 16-10, Moscow 117997, Russia
基金
俄罗斯科学基金会;
关键词
TUMORS; CELLS; PROTEINS;
D O I
10.1364/OL.43.003152
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
While laser scanning fluorescence lifetime imaging (FLIM) is a powerful approach for cell biology, its small field of view (typically less than 1 mm) makes it impractical for the imaging of large biological samples that is often required for biomedical applications. Here we present a system that allows performing FLIM on macroscopic samples as large as 18 mm with a lateral resolution of 15 mu m. The performance of the system is verified with FLIM of endogenous metabolic cofactor reduced nicotinamide adenine dinucleotide (phosphate), NAD(P)H, and genetically encoded fluorescent protein mKate2 in a mouse tumor in vivo. (C) 2018 Optical Society of America
引用
收藏
页码:3152 / 3155
页数:4
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