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Synthesis and evaluation of new iodine-125 radiopharmaceuticals as potential tracers for malignant melanoma.

作者信息

Michelot J M, Moreau M F, Labarre P G, Madelmont J C, Veyre A J, Papon J M, Parry D F, Bonafous J F, Boire J Y, Desplanches G G

机构信息

INSERM U 71, B.P. 184, Clermont-Ferrand, France.

出版信息

J Nucl Med. 1991 Aug;32(8):1573-80.

PMID:1869982
Abstract

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.

摘要

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