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J Nucl Med ; 32(8): 1573-80, 1991 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-1869982

RESUMO

The synthesis, labeling, and biodistribution of four 125I radiopharmaceuticals designed to localize in melanoma were tested. Uptake in tumors was demonstrated by autoradiography of whole-body sections and quantitated by measurement of radioactivity of selected tissues and tumors using melanoma-bearing mice. N-(2-diethylaminoethyl)-4-iodobenzamide was selected for its highest melanoma uptake: 60 min after IV injection of 6.5% and 4% ID/g, respectively for murine B16 and human melanotic melanoma. Tumor uptake showed the highest values of all analyzed tissues from 6 to 24 hr after injection. High uptake in melanotic tumor tissue with relatively low uptake in blood, muscle, brain, lung, and liver tissue resulted in high tumor/nontumor ratios (at 24 hr for B16, tumor/blood = 37, tumor/brain = 147, tumor/muscle = 95). This agent was compared with iodoamphetamine. Scintigraphic images of the tumor confirmed that external detection of melanoma is possible with this new radiopharmaceutical.


Assuntos
Benzamidas , Radioisótopos do Iodo , Melanoma Experimental/diagnóstico por imagem , Anfetaminas , Animais , Benzamidas/síntese química , Iofetamina , Masculino , Camundongos , Camundongos Endogâmicos , Cintilografia , Distribuição Tecidual
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