scholarly journals One- and two-photon time-resolved fluorescence of visible and near-infrared dyes in scattering media

2009 ◽  
Author(s):  
R. Esposito ◽  
C. Altucci ◽  
R. Velotta ◽  
G. M. Gaeta ◽  
M. Lepore
2000 ◽  
Vol 651 ◽  
Author(s):  
Sangmin Jeon ◽  
Sung Chul Bae ◽  
Jiang John Zhao ◽  
Steve Granick

AbstractTwo-photon time-resolved fluorescence anisotropy methods were used to study the dynamical environment when fluorescent-labelled DNA oligomers (labelled with FAM, 6-fluorescein-6-carboxamido hexanoate) formed surface complexes with quaternized polyvinylpyridine (QPVP) cationic layers on a glass surface. We compared the anisotropy decay of DNA in bulk aqueous solution, DNA adsorbed onto QPVP, and QPVP-DNA-QPVP sandwich structures. When DNA was adsorbed onto QPVP, its anisotropy decay was dramatically retarded compared to the bulk, which means it had very slow rotational motion on the surface. Motions slowed down with increasing salt concentration up to a level of 0.1 M NaCl, but mobility began to increase at still higher salt concentration owing to detachment from the surface-immobilizing QPVP layers.


2019 ◽  
Vol 28 (01) ◽  
pp. 1950003 ◽  
Author(s):  
Yaochuan Wang ◽  
Yizhuo Wang ◽  
Guiqiu Wang ◽  
Dajun Liu

A series of branched styryl derivatives based on 1,3,5-triazine were studied by nonlinear optical property measurement, degenerated pump-probe, and time-resolved fluorescence anisotropy methods to elucidate the two-photon absorption (TPA) properties and intramolecular interactions between branches. Significant enhancement of the TPA cross-section was observed in multi-branched derivatives. The anisotropy of multi-branched compounds shows faster decay and small residual values, indicating strong intramolecular interactions between branches, which further confirmed the TPA enhancement mechanism.


2021 ◽  
Vol 11 (24) ◽  
pp. 11596
Author(s):  
Elisabeta I. Szerb ◽  
Sharmistha Chatterjee ◽  
Massimo La Deda ◽  
Giovanna Palermo ◽  
Lucie Sancey ◽  
...  

This work reports the study of two-photon induced properties of a highly luminescent cyclometalated Ir(III) complex, [Ir(ppy)2(en)] OOCCH3 (1), ppy = 2-phenylpyridine, en = ethylenediamine. Steady-state and time-resolved fluorescence measurements were performed by exciting 1 at the biologically relevant wavelength of 800 nm, whereas, the generation of singlet oxygen (1O2) was evaluated using 9,10-Anthracenediyl-bis(methylene)dimalonic acid (ABDA) as a detection probe. Preliminary in vitro experiments with U87-MG cells were performed, showing the potential of this compound as a two-photon photodynamic therapy (2P-PDT) agent at NIR wavelengths.


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