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1.
Mol Imaging Biol ; 16(2): 255-63, 2014 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-24101374

RESUMEN

PURPOSE: Glucagon-like peptide-1 receptor (GLP-1R) is a molecular target for imaging of pancreatic beta cells. We compared the ability of [Nle(14),Lys(40)(Ahx-NODAGA-(64)Cu)NH2]-exendin-4 ([(64)Cu]NODAGA-exendin-4) and [Nle(14),Lys(40)(Ahx-NODAGA-(68)Ga)NH2]-exendin-4 ([(68)Ga]NODAGA-exendin-4) to detect native pancreatic islets in rodents. PROCEDURES: The stability, lipophilicity and affinity of the radiotracers to the GLP-1R were determined in vitro. The biodistribution of the tracers was assessed using autoradiography, ex vivo biodistribution and PET imaging. Estimates for human radiation dosimetry were calculated. RESULTS: We found GLP-1R-specific labelling of pancreatic islets. However, the pancreas could not be visualised in PET images. The highest uptake of the tracers was observed in the kidneys. Effective dose estimates for [(64)Cu]NODAGA-exendin-4 and [(68)Ga]NODAGA-exendin-4 were 0.144 and 0.012 mSv/MBq, respectively. CONCLUSION: [(64)Cu]NODAGA-exendin-4 might be more effective for labelling islets than [(68)Ga]NODAGA-exendin-4. This is probably due to the lower specific radioactivity of [(68)Ga]NODAGA-exendin-4 compared to [(64)Cu]NODAGA-exendin-4. The radiation dose in the kidneys may limit the use of [(64)Cu]NODAGA-exendin-4 as a clinical tracer.


Asunto(s)
Acetatos , Complejos de Coordinación , Radioisótopos de Cobre , Compuestos Heterocíclicos con 1 Anillo , Células Secretoras de Insulina/diagnóstico por imagen , Péptidos , Tomografía de Emisión de Positrones/métodos , Coloración y Etiquetado , Acetatos/química , Acetatos/farmacocinética , Secuencia de Aminoácidos , Animales , Autorradiografía , Complejos de Coordinación/química , Complejos de Coordinación/farmacocinética , Radioisótopos de Galio , Tracto Gastrointestinal/diagnóstico por imagen , Tracto Gastrointestinal/patología , Compuestos Heterocíclicos con 1 Anillo/química , Compuestos Heterocíclicos con 1 Anillo/farmacocinética , Humanos , Masculino , Datos de Secuencia Molecular , Péptidos/química , Péptidos/farmacocinética , Radiometría , Ratas , Ratas Sprague-Dawley , Distribución Tisular , Tomografía Computarizada por Rayos X
2.
Nucl Med Biol ; 30(3): 225-32, 2003 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-12745013

RESUMEN

The purpose of the present study was to establish the tissue distribution in abdominal organs and the excretion of radioactivity after intravenous administration of [(111)In-DTPA-D-Phe(1)]-octreotide in healthy dogs. In five Beagle dogs computed tomography and single photon emission computed tomography (SPECT) at 24 h after injection of [(111)In-DTPA-D-Phe(1)]-octreotide revealed accumulation of radioactivity in the kidneys, gall bladder, gastric fundus and cardia, intestinal tract, but not in the spleen. These findings were confirmed by in vitro scintigraphy of single abdominal organs. This also demonstrated accumulation of radioactivity in the pancreas and located the radioactivity in the gastrointestinal tract primarily in the wall itself. In vitro autoradiography with (125)I-[Tyr(3)]-octreotide on tissue samples in two dogs revealed sst receptors in the medullary part of the kidney, the basal two-thirds of the gastric mucosa of the cardia and fundus, Peyer's patches and neural plexus of the gastrointestinal tract. No sst receptors were demonstrated in the liver, spleen, and pancreas. These results differ to findings in man, where there is uptake in the spleen but not in the stomach, most likely caused by interspecies variations in sst receptor subtype expression.


Asunto(s)
Octreótido/análogos & derivados , Octreótido/farmacocinética , Ácido Pentético/análogos & derivados , Ácido Pentético/farmacocinética , Radiofármacos/farmacocinética , Animales , Autorradiografía , Perros , Inyecciones Intravenosas , Masculino , Distribución Tisular , Tomografía Computarizada de Emisión de Fotón Único
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