Deep-red to near-infrared fluorescent dyes: Synthesis, photophysical properties, and application in cell imaging

Author(s):  
Qi Li ◽  
Weimin Liu ◽  
Jiasheng Wu ◽  
Bingjiang Zhou ◽  
Guangle Niu ◽  
...  
2015 ◽  
Vol 1786 ◽  
pp. 1-6 ◽  
Author(s):  
Aneshkumar Tilwani ◽  
Hildegarde Bell ◽  
Jose Alvarez ◽  
Belqais Naqshbandi ◽  
Folarin Erogbogbo

ABSTRACTGraphene Quantum Dots (GQDs) are of interest to the biomedical community due to their unique fluorescence properties, which may be advantageous for biology and medicine. Advantages of this graphene nanomaterial over fluorescent dyes for biomedical imaging include bright emission, easy surface modification, biocompatibility, and anticipated low toxicity. We hypothesize that GQDs with desirable fluorescence properties which can be used for effective biomedical imaging (such as near infrared emission) may be synthesized from cheap carbon sources. Here, we show that these fluorescent GQDs are fabricated in a facile wet chemistry route using activated charcoal as the starting material. The GQDs were characterized with AFM, TEM, FTIR, PL spectroscopy, Raman spectroscopy and animal imaging techniques. The particles were visible in animals indicating their potential for biomedical imaging. The GQDs exhibited excitation that spanned the UV and visible ranges and emission that spanned the visible and near infrared ranges. The GQDs were an average of 4 nm in height, crystalline, from 1 to 60 nm in size. The GQDs were consistent with the presence of graphene and the following functional groups: C-O, C-H, C=C, and CO2H. In conclusion, GQDs with favorable photophysical properties can be produced from affordable and widely available raw materials for imaging and other biomedical application purposes.


2019 ◽  
Author(s):  
Arundhati Deshmukh ◽  
Danielle Koppel ◽  
Chern Chuang ◽  
Danielle Cadena ◽  
Jianshu Cao ◽  
...  

Technologies which utilize near-infrared (700 – 1000 nm) and short-wave infrared (1000 – 2000 nm) electromagnetic radiation have applications in deep-tissue imaging, telecommunications and satellite telemetry due to low scattering and decreased background signal in this spectral region. However, there are few molecular species, which absorb efficiently beyond 1000 nm. Transition dipole moment coupling (e.g. J-aggregation) allows for redshifted excitonic states and provides a pathway to highly absorptive electronic states in the infrared. We present aggregates of two cyanine dyes whose absorption peaks redshift dramatically upon aggregation in water from ~ 800 nm to 1000 nm and 1050 nm with sheet-like morphologies and high molar absorptivities (e ~ 10<sup>5 </sup>M<sup>-1</sup>cm<sup>-1</sup>). To describe this phenomenology, we extend Kasha’s model for J- and H-aggregation to describe the excitonic states of <i> 2-dimensional aggregates</i> whose slip is controlled by steric hindrance in the assembled structure. A consequence of the increased dimensionality is the phenomenon of an <i>intermediate </i>“I-aggregate”, one which redshifts yet displays spectral signatures of band-edge dark states akin to an H-aggregate. We distinguish between H-, I- and J-aggregates by showing the relative position of the bright (absorptive) state within the density of states using temperature dependent spectroscopy. Our results can be used to better design chromophores with predictable and tunable aggregation with new photophysical properties.


ACS Omega ◽  
2021 ◽  
Author(s):  
Yoshio Nakahara ◽  
Yukiho Nakajima ◽  
Soichiro Okada ◽  
Jun Miyazaki ◽  
Setsuko Yajima

Materials ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1098
Author(s):  
Agata Blacha-Grzechnik

For many years, the research on conjugated polymers (CPs) has been mainly focused on their application in organic electronics. Recent works, however, show that due to the unique optical and photophysical properties of CPs, such as high absorption in UV–Vis or even near-infrared (NIR) region and efficient intra-/intermolecular energy transfer, which can be relatively easily optimized, CPs can be considered as an effective light-activated source of versatile and highly reactive singlet oxygen for medical or catalytic use. The aim of this short review is to present the novel possibilities that lie dormant in those exceptional polymers with the extended system of π-conjugated bonds.


2015 ◽  
Vol 6 (21) ◽  
pp. 3962-3969 ◽  
Author(s):  
Chunhui Dai ◽  
Dongliang Yang ◽  
Wenjie Zhang ◽  
Biqing Bao ◽  
Yixiang Cheng ◽  
...  

We prepared a series of novel chiral far-red/near-infrared fluorescent CPNs with different nanoparticle sizes, which show size-dependent chirality and are successfully employed for cell imaging.


2012 ◽  
Vol 393 (1-2) ◽  
pp. 23-35 ◽  
Author(s):  
Markus Hirsch ◽  
Dennis Strand ◽  
Mark Helm

Abstract Investigations into the fate of small interfering RNA (siRNA) after transfection may unravel new ways to improve RNA interference (RNAi) efficiency. Because intracellular degradation of RNA may prevent reliable observation of fluorescence-labeled siRNA, new tools for fluorescence microscopy are warranted to cover the considerable duration of the RNAi effect. Here, the characterization and application of new fluorescence resonance energy transfer (FRET) dye pairs for sensing the integrity of duplex siRNA is reported, which allows an assessment of the degradation status of an siRNA cell population by live cell imaging. A panel of high-yield fluorescent dyes has been investigated for their suitability as FRET pairs for the investigation of RNA inside the cell. Nine dyes in 13 FRET pairs were evaluated based on the performance in assays of photostability, cross-excitation, bleed-through, as well as on quantified changes of fluorescence as a consequence of, e.g., RNA strand hybridization and pH variation. The Atto488/Atto590 FRET pair has been applied to live cell imaging, and has revealed first aspects of unusual trafficking of intact siRNA. A time-lapse study showed highly dynamic movement of siRNA in large perinuclear structures. These and the resulting optimized FRET labeled siRNA are expected to have significant impact on future observations of labeled RNAs in living cells.


2014 ◽  
Vol 18 (08n09) ◽  
pp. 752-761 ◽  
Author(s):  
Tetsuo Okujima ◽  
Yoichi Shida ◽  
Keishi Ohara ◽  
Yuya Tomimori ◽  
Motoyoshi Nishioka ◽  
...  

A series of O-chelated BODIPYs fused with aromatic rings such as benzene and acenaphthylene at β,β-positions was synthesized as a near-infrared dye. The photophysical properties were examined by UV-vis-NIR absorption and fluorescence measurement. Acenaphthylene-fused O-BODIPYs showed a intense absorption at 750–840 nm with the ε of 105 M-1.cm-1. and a fluorescence emission at 770–850 nm with the high Φ value of 0.06–0.43.


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