Fluorescence probe characterization tool

Pyridin-lndoles 2-Pyridin-2-yl-lff-indole derivatives were described by the University of Athens [138]. It was aimed for to identify fluorescent probes as tools to characterize cellular binding sites of ERs. It was found that several members of this family (e.g. 104 and 105) exhibit reasonable good binding activities. Whether these compounds behave as agonists or antagonists is currently unknown. No data on subtype selectivity were disclosed. 

In the last decade confocal laser scanning microscopy (CLSM) was shown to be a helpful tool for various further tasks of microparticle characterization (Lamprecht et al., 2000a, b, c). It minimizes the light scattered from out-of-focus structures, and permits the identification of several compounds through use of different fluorescence labels. Therefore, CLSM can be applied as a non-destructive visualization technique for microparticles. Moreover, CLSM allows visualization and characterization of structures not only on the surface, but also inside the particles, provided the carrier matrices are sufficiently transparent and can be fluorescently labeled by collecting several coplanar cross-sections, a three-dimensional reconstruction of the inspected objects is possible. Figure 6.13 shows the application of CLSM to investigatation of the cross-sectional structures of spray-dried powders of maltodextrin (MD) with a dextrose equivalent value of DE = 2 and 20. Florescein sodium salt was dissolved in the feed solution as a fluorescent probe of the carrier... 

Fluorescence is an excellent tool to probe chemical microenvironments. For example, in 2010, Martin et al. used a specific shift in fluorescence emission spectra of polar sensitive fluorophores, for example, acrylodan, to characterize the polarity immediately surrounding immobilized enzymes [34]. Cytoplasmic malate dehydrogenase (cMDH) and mitochondrial malate dehydrogenase (mMDH), for example, were tagged with fluorescent probes and then entrapped within macroporous three-dimensional chitosan scaffolds. A blue shift in the acrylodan emission maximum was taken to indicate a polar shift in the chemical microenvironment directly surrounding enzymes immobilized within the scaffold (Figme 12.5). The emission... 

The time-resolved spectroscopy is a sensitive tool to study the solute-solvent interactions. The technique has been used to characterize the solvating environment in the solvent. By measuring the time-dependent changes of the fluorescence signals in solvents, the solvation, rotation, photoisomerization, or excimer formation processes of a probe molecule can be examined. In conventional molecular solutions, many solute-solvent complexes. 

Electron microprobes can be used in spot mode to measure the chemical compositions of individual minerals. Mineral grains with diameters down to a few microns are routinely measured. The chemical composition of the sample is determined by comparing the measured X-ray intensities with those from standards of known composition. Sample counts must be corrected for matrix effects (absorption and fluorescence). The spatial resolution of the electron microprobe is governed by the interaction volume between the electron beam and the sample (Fig. A.l). An electron probe can also be operated in scanning mode to make X-ray maps of a sample. You will often see false-color images of a sample where three elements are plotted in different colors. Such maps allow rapid identification of specific minerals. EMP analysis has become the standard tool for characterizing the minerals in meteorites and lunar samples. 

Baxter DF, Kirk M, Garcia AF et al. (2002) A novel membrane potential-sensitive fluorescent dye improves cell-based assays for ion channels. J Biomol Screen 7(1) 79—85 Epps DE, Wolfe ML, Groppi V (1994) Characterization of the steady-state and dynamic fluorescence properties of the potential-sensitive dye bis-(l,3-dibutylbarbituric acid)trimethine oxonol (BiBAC4(3)) in model systems and cells. Chem Phys Lipids 69(2) 137—150 Gonzalez JE, Maher MP (2002) Cellular fluorescent indicators and voltage/ion probe reader (VIPR(TM)) tools for ion channel and receptor drug discovery. Recept Channels 8(5—6) 283—295... 

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