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Labeling of blood cells with /sup 99m/Tc
Erythrocytes, leukocytes, and tumor cells were labeled with /sup 99m/Tc to take advantage of the ideal physical properties of /sup 99m/Tc. Clinical studies indicate that labeled erythrocytes can be used to obtain improved vascular and splenic imaging as well as reliable red cell volumes. The erythrocytes have been labeled with and without the use of an added reducing agent. Two methods of adding the reducing agent stannous chloride have been proposed which differ in the order of addition of the stannous ion and the pertechnetate. The preliminary reports of labeling of leukocytes and tumor cells offer hope that further development will result in truly specific radiopharmaceuticals. (auth
Why does the agonist [(18)F]FP-TZTP bind preferentially to the M(2) muscarinic receptor?
Purpose: Preferential binding of FP-TZTP at the M2 receptor in vivo led to investigation of [18F]FP-TZTP as a potential PET tracer for Alzheimer's disease, in which a substantial reduction of M2 receptors has been observed in autopsy studies. We hereby investigated in vitro the FP-TZTP behavior to further elucidate the properties of FP-TZTP that lead to its M2 selectivity. Methods: Chinese hamster ovarian cells expressing the five subtypes of human muscarinic receptor as well as the wild type were harvested in culture to assess equilibrium binding. Specific binding was calculated by subtraction of non-specific binding from total binding. Internal specific binding was calculated by subtraction of external specific binding from the total specific binding. Saturation assays were also performed to calculate Bmax, Ki, and IC50. In addition, equilibrium binding and dissociation kinetic studies were performed on rat brain tissue. Selected regions of interest were drawn on the digital autoradiograms and [18F]FP-TZTP off-rates were determined by measurement of the rate of release into a buffer solution of [18F]FP-TZTP from slide-bound cells that had been preincubated with [18F]FP-TZTP. Results: At equilibrium in vitro, M2 subtype selectivity of [18F]FP- TZTP was not evident. We demonstrated that ATP-dependent mechanisms are not responsible for FP-TZTP M2 selectivity. In vitro off-rate studies from rat brain tissue showed that the off-rate of FP-TZTP varied with the percentage of M2 subtype in the tissue region. Conclusion: The slower dissociation kinetics of FP-TZTP from M2 receptors compared with the four other muscarinic receptor subtypes may be a factor in its M2 selectivity