Fig. 6.
Fig. 6. Platelet counts were measured in healthy SCID/NOD mice that received different treatments for the toxicity of213Bi (initially at weekly and subsequently at monthly intervals). / Mice in the control group did not receive any treatment (control). Mice in another group received 250 μCi (9.25 MBq)213Bi–DOTA-biotin without pretargeting and sCA (Bi-250 alone), and mice in remaining groups received 400 μg HAT-SA pretargeting for 24 hours, 100 μg sCA for 4 hours, followed by 100 μCi (3.7 MBq; Bi-100) or 250 μCi (9.25 MBq; Bi-250) or 500 μCi (18.5 MBq; Bi-500) 213Bi–DOTA-biotin. Mice in the combination group received the same pretargeting, clearing steps and 250 μCi (9.25 MBq) 213Bi–DOTA-biotin followed by 100 μg HAT once per week for 4 weeks.

Platelet counts were measured in healthy SCID/NOD mice that received different treatments for the toxicity of213Bi (initially at weekly and subsequently at monthly intervals).

Mice in the control group did not receive any treatment (control). Mice in another group received 250 μCi (9.25 MBq)213Bi–DOTA-biotin without pretargeting and sCA (Bi-250 alone), and mice in remaining groups received 400 μg HAT-SA pretargeting for 24 hours, 100 μg sCA for 4 hours, followed by 100 μCi (3.7 MBq; Bi-100) or 250 μCi (9.25 MBq; Bi-250) or 500 μCi (18.5 MBq; Bi-500) 213Bi–DOTA-biotin. Mice in the combination group received the same pretargeting, clearing steps and 250 μCi (9.25 MBq) 213Bi–DOTA-biotin followed by 100 μg HAT once per week for 4 weeks.

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