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Single photon emission compound

In a comparative study, [ F]FDHR, the well-known extractable MBF SPECT (single photon emission computed tomography) tracer p° TI]TICI, and the vascular reference tracer [ l]albumin were evaluated in 22 isolated erythrocyte- and albumin-perfused rabbit hearts. A superior retention of [ F]FDHR was observed and the net uptake of this F-labeled compound was better correlated with the blood flow than that of p° TI]TICI, indicating that [ F]FDHR is a better flow tracer than p° TI]TICI in isolated rabbit hearts [72]. [Pg.98]

Nowadays, nuclear medicine has become an indispensible section of medical science, and the production of radionuclides and labelled compounds for application in nuclear medicine is an important branch of nuclear and radiochemistry. The development of radionuclide generators made short-lived radionuclides available at any time for medical application. New imaging devices, such as single photon emission tomography (SPET) and positron emission tomography (PET) made it possible to study local biochemical reactions and their kinetics in the living human body. [Pg.373]

When a patient sees a doctor because of heart trouble, the doctor has many options depending on his suspicions. One rather elaborate way to diagnose is to inject a radiotechnetium compound into the blood stream, followed by an analytical method known as single photon emission computed tomography (SPECT). A rotating gamma camera measures the radioactivity at short intervals providing, with the help of a computer, a reconstructed picture, which enables the physician to determine how much of the heart muscle is deprived of blood. [Pg.78]

I-5-iodo-6-nitroquipazine was administered to the primate Macaca mulatto in testing the suitability of the compound for the in vivo imaging of 5-HT transporter sites in the brain by single photon emission computer tomography SPECT [92]. [Pg.354]

Compounds labeled with isotopes have played an important role in chemistry, biology, and medicine since they were first used as tracers by Hevesey. - Both stable - and radioactive isotopes were utilized in early investigations, but the situation changed dramatically with the invention of the cyclotron by Lawrence in 1930 and the construction of the nuclear reactor by Fermi in 1942 that enabled access to radioisotopes on a regular basis. Radioisotope use in medicine was also accelerated by advances in radiation-detection techniques. The development of single-photon emission computerized tomography (SPECT) " and positron emission tomography revolutionized... [Pg.91]

Similarly to the PET technique, single photon emission computed tomography (SPECT) is an imaging procedure in which a radionuclide-labeled biomolecule is injected and monitored. Once the biochemical compound enters the bloodstream, it travels to body organs (brain, liver, kidney, heart, and the peripheral vascular system) and is absorbed by them according to each organ s affinity for the particular compound (Gullberg et al., 2010). [Pg.223]

Another use of computation was in single-photon counting. This method of obtaining fluorescent lifetimes involves use of a lamp with, for example, nanosecond-width lamp flashes directed toward a fluorescent compound. At each time, t, a number of molecules are excited and begin to decay with emission. The emission intensity at time t is given by Equation 1.3. For simplicity of presentation here we assume a single negative exponential excited-state decay function as in Equation 1.4. [Pg.14]

Indium compounds give a blue-violet flame test. The atomic emission responsible for this blue-violet color has a wavelength of 451 nm. Obtain the energy of a single photon of this wavelength. [Pg.290]

QDs excited by single or multiple photons exhibit multixponen-tial decays, in our hands generally with two components of <10 and 10-25 ns. This property renders the nanoparticles useful reagents for the systematic modulation of emission via a technique we have denoted as photochromic FRET (pcFRET, Fig. 12.5 see [1, 2, 134]). The method was developed in order to circumvent inherent limitations in the quantitative determination of FRET in cells, particularly in imaging applications. We have classified pcFRET as a member of the family of so-called acceptor depletion methods [1, 2] due to the reversible change in the structure, and thus spectroscopic properties, of the photochromic compound (e.g., a diheteroarylethene) serving as the FRET acceptor. The key... [Pg.510]


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Photon emission

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