Color‐Tunable Light‐up Bioorthogonal Probes for In Vivo Two‐Photon Fluorescence Imaging

2020 ◽  
Vol 26 (20) ◽  
pp. 4576-4582 ◽  
Author(s):  
Yandong Dou ◽  
Yajun Wang ◽  
Yukun Duan ◽  
Bin Liu ◽  
Qinglian Hu ◽  
...  
2015 ◽  
Vol 3 (5) ◽  
pp. 646-651 ◽  
Author(s):  
Pei-Pei Yang ◽  
Yang Yang ◽  
Yu-Juan Gao ◽  
Yi Wang ◽  
Ju-Chen Zhang ◽  
...  

2015 ◽  
Vol 3 (36) ◽  
pp. 7213-7221 ◽  
Author(s):  
Qiong Zhang ◽  
Xiaohe Tian ◽  
Zhangjun Hu ◽  
Caroline Brommesson ◽  
Jieying Wu ◽  
...  

TPA cross sections are enhanced for the complexes containing D–A type ligandL1.1exhibits specificity in two-photon fluorescence imaging.


2004 ◽  
Vol 99 (4) ◽  
pp. 235-245 ◽  
Author(s):  
Claudiu C. Gradinaru ◽  
Peter Martinsson ◽  
Thijs J. Aartsma ◽  
Thomas Schmidt

2014 ◽  
Vol 522 (8) ◽  
pp. 1708-1727 ◽  
Author(s):  
Sarah E. Crowe ◽  
Graham C.R. Ellis-Davies

2005 ◽  
Author(s):  
Tsung-Han Tsai ◽  
Szu-Yu Chen ◽  
Shih-Peng Tai ◽  
Cheng-Yung Lin ◽  
Huai-Jen Tsai ◽  
...  

2020 ◽  
Author(s):  
Raphaël Turcotte ◽  
Carla C. Schmidt ◽  
Martin J. Booth ◽  
Nigel J. Emptage

Multimode optical fibers (MMFs), combined with wavefront control methods, have achieved minimally-invasive in vivo imaging of neurons in deep-brain regions with diffraction-limited spatial resolution. Here, we report a method for volumetric two-photon fluorescence imaging with a MMF-based system requiring a single transmission matrix measurement. Central to this method is the use of a laser source able to generate both continuous wave light and femtosecond pulses. The chromatic spreading of pulses generated an axially elongated excitation focus, which we used to demonstrate volumetric imaging of neurons and their dendrites in live rat brain slices through a 60 μm-core MMF.


2015 ◽  
Vol 54 (34) ◽  
pp. 10044 ◽  
Author(s):  
Gerardo Estrada ◽  
Christopher Beetle ◽  
James Schummers

2016 ◽  
Vol 52 (97) ◽  
pp. 13991-13994 ◽  
Author(s):  
Wei Zhang ◽  
Junqing Kang ◽  
Ping Li ◽  
Lu Liu ◽  
Hui Wang ◽  
...  

We have designed and synthesized an SA-imprinted conjugated polymer nanoprobe with two-photon fluorescence properties, which exhibits specific recognition ability to the target SA and has been used for monitoring sialylated glycan levels selectively in vivo.


2020 ◽  
Vol 8 ◽  
Author(s):  
Qing Lu ◽  
Cheng-Juan Wu ◽  
Zhiqiang Liu ◽  
Guangle Niu ◽  
Xiaoqiang Yu

Fluorescence imaging has been widely used as a powerful tool for in situ and real-time visualization of important analytes and biological events in live samples with remarkably high selectivity, sensitivity, and spatial resolution. Compared with one-photon fluorescence imaging, two-photon fluorescence imaging exhibits predominant advantages of minimal photodamage to samples, deep tissue penetration, and outstanding resolution. Recently, the aggregation-induced emission (AIE) materials have become a preferred choice in two-photon fluorescence biological imaging because of its unique bright fluorescence in solid and aggregate states and strong resistance to photobleaching. In this review, we will exclusively summarize the applications of AIE-active materials in two-photon fluorescence imaging with some representative examples from four aspects: fluorescence detection, in vitro cell imaging, ex vivo tissue imaging, and in vivo vascular imaging. In addition, the current challenges and future development directions of AIE-active materials for two-photon bioimaging are briefly discussed.


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