Fluorescence three-dimensional

Bhawalkar J D, Swiatkiewicz J, Pan S J, Samarabandu J K, Liou W S, He G S, Berezney R, Cheng P C and Prasad P N 1996 Three-dimensional laser scanning two-photon fluorescence confocal microscopy of polymer materials using a new, efficient upconverting fluorophore Scanning 18 562-6... 

Figure Bl.22.11. Near-field scanning optical microscopy fluorescence image of oxazine molecules dispersed on a PMMA film surface. Each protuberance in this three-dimensional plot corresponds to the detection of a single molecule, the different intensities of those features being due to different orientations of the molecules. Sub-diffraction resolution, in this case on the order of a fraction of a micron, can be achieved by the near-field scaiming arrangement. Spectroscopic characterization of each molecule is also possible. (Reprinted with pennission from [82]. Copyright 1996 American Chemical Society.)...

Spectroscopic properties of 5 were studied (OOMIll). Spectral characteristics of 5 of 0.1 N NaOH solution were investigated by UV spectroscopy (97MI17). Three dimensional fluorescent spectral characteristics of fluoroquinolones, including 5, were studied in varying media (00SA(A)1787). The structure of 8 was confirmed by UV and IR studies (98MI89). 

Figure 3. Three-dimensional plot of the room-temperature fluorescence of a mixture of 500 ng each of benzo(a)pyrene and benzo(e)pyrene on 80% q-cyclodextrin-NaCl. Numbers along dashed lines show the approximate wavelengths (nm) represented by these lines. The excitation wavelength was varied from 250 nm (front spectrum) to 370 nm (back spectrum) at 2-nm increments. Benzo(a)pyrene emitted from approximately 380 nm to 540 nm, and benzo(e)pyrene emitted from 365 nm to 505 nm.

The NIR femtosecond laser microscope realized higher order multi photon excitation for aromatic compounds interferometric autocorrelation detection of the fluorescence from the microcrystals of the aromatic molecules confirmed that their excited states were produced not via stepwise multiphoton absorption but by simultaneous absorption of several photons. The microscope enabled us to obtain three-dimensional multiphoton fluorescence images with higher spatial resolution than that limited by the diffraction theory for one-photon excitation. 

Zinc carboxylate interactions have been exploited as part of a fluorescent molecular sensor for uronic acids. The sensors feature two interactions coordination of the carboxylate to the zinc and a boronic acid diol interaction.389 Photoluminescent coordination polymers from hydrothermal syntheses containing Zn40 or Zn4(OH)2 cores with isophthalate or fumarate and 4,4 -bipyridine form two- and three-dimensional structures. Single X-ray diffraction of both dicarboxylates identified the network structure.373... 

Two-dimensional excitation experiments (two wavelengths excitation in fluorescence spectroscopy or two frequency experiments in 2D-NMR) also generate three-dimensional signal functions. 

Diaspro A, Robello M (2000) Two-photon excitation of fluorescence for three-dimensional optical imaging of biological structures. J Photochem Photobiol B 55 1-8... 

Noise can be also introduced by biochemical heterogeneity of the specimen. This can be a major cause of uncertainty in biological imaging. The high (three-dimensional) spatial resolution of fluorescence microscopy results in low numbers of fluorophores in the detection volume. In a typical biological sample, the number of fluorophores in the detection volume can be as low as 2-3 fluorophores for a confocal microscope equipped with a high NA objective at a fluorescent dye concentration of 100 nM. This introduces another source of noise for imaging applications, chemical or molecular noise, related to the inherent randomness of diffusion and the interaction of molecules. 

Straub, M. and Hell, S. W. (1998). Fluorescence lifetime three-dimensional microscopy with picosecond precision using a multifocal multiphoton microscope. Appl. Phys. Lett. 73, 1769-71. 

Godavarty, A., Sevick-Muraca, E. M. and Eppstein, M. J. (2005). Three-dimensional fluorescence lifetime tomography. Med. Phys. 32, 992-1000. 

Dendrimers can be used to effectively coat and passivate fluorescent quantum dots to make biocompatible surfaces for coupling proteins or other biomolecules. In addition, the ability of dendrimers to contain guest molecules within their three-dimensional structure also has led to the creation of dendrimer-metal nanoclusters having fluorescent properties. In both applications, dendrimers are used to envelop metal or semiconductor nanoparticles that possess fluorescent properties useful for biological detection. 

D X-ray fluorescence analysis, 20 439-440 Three-dimensional (3D) transistor structures, in scaling to deep submicron dimensions, 22 256 Three-dimensional carbon-carbon composites, 26 774... 

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