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Bioimaging luminescence microscopy

An example of the utility of the time-resolved technique in eliminating the interference from background fluorescence in bioimaging is shown in Figure 13.17b. Nagano and coworkers compared time-resolved luminescence microscopy with conventional microscopy using live cultured HeLa cells injected with a Eu + complex Eu-36 (or Eu-37). In the prompt fluorescence images, both the luminescence of Eu-36 (or Eu-37) and weak autofluorescence from... [Pg.542]

Multiphoton or two-photon laser scanning microscopy is an alternative to confocal and time-resolved microscopy for bioimaging applications. The principle has been discussed in Lanthanides Luminescence Applications and concerns a two-photon excitation from the simultaneous absorption of two photons in a single quantized event. A bioprobe that normally absorbs ultraviolet light (Xex = 350 nm) can also be excited by two photons of NIR light, at 700 nm (the wavelength is twice that required for one-photon excitation). These two photons must interact simultaneously, which means in a very small lapse time. The instrumentation requires pulse lasers to provide sufficient power, as the photon density must... [Pg.556]

The first two chapters of this work cover theoretical and practical aspects of the emission process, the spectroscopic techniques and the equipment used to characterize the emission. Chapter 3 introduces and reviews the property of circularly polarized emission, while Chapter 4 reviews the use of lanthanide ion complexes in bioimaging and fluorescence microscopy. Chapter 5 covers the phenomenon of two-photon absorption, its theory as well as applications in imaging, while Chapter 6 reviews the use of lanthanide ions as chemo-sensors. Chapter 7 introduces the basic principles of nanoparticle upconversion luminescence and its use for bioimaging and Chapter 8 reviews direct excitation of the lanthanide ions and the use of the excitation spectra to probe the metal ion s coordination environment in eoordination compounds and biopolymers. Finally, Chapter 9 describes the formation of heterobimetallic complexes, in whieh the lanthanide ion emission is promoted through the hetero-metal. [Pg.386]


See other pages where Bioimaging luminescence microscopy is mentioned: [Pg.212]    [Pg.552]    [Pg.144]    [Pg.179]    [Pg.190]    [Pg.556]    [Pg.558]    [Pg.102]    [Pg.364]    [Pg.557]    [Pg.124]    [Pg.68]    [Pg.177]    [Pg.223]   
See also in sourсe #XX -- [ Pg.4 , Pg.127 ]




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Bioimaging

Bioimaging luminescence

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