Figure 1
Figure 1. Biodistributions of [213Bi]DOTA-biotin in tumor, blood, and normal organs after PRIT with 1F5-SA or CC49-SA FPs. Athymic mice bearing Ramos xenografts were injected with 2.8nM each unlabeled FP followed 20 hours later by 5.8nM CA, and 4 hours after that by 1.2nM [213Bi]DOTA-biotin. Groups of 5 mice were euthanized 10, 45, 90, and 180 minutes after the injection of [213Bi]DOTA-biotin. The radioactivity in the tissues were quantified by gamma counting, corrected for decay, and expressed as the % ID/g of tissue.

Biodistributions of [213Bi]DOTA-biotin in tumor, blood, and normal organs after PRIT with 1F5-SA or CC49-SA FPs. Athymic mice bearing Ramos xenografts were injected with 2.8nM each unlabeled FP followed 20 hours later by 5.8nM CA, and 4 hours after that by 1.2nM [213Bi]DOTA-biotin. Groups of 5 mice were euthanized 10, 45, 90, and 180 minutes after the injection of [213Bi]DOTA-biotin. The radioactivity in the tissues were quantified by gamma counting, corrected for decay, and expressed as the % ID/g of tissue.

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