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Preparation and evaluation of two super(188)Re-radiopharmaceuticals for endovascular irradiation
Procedures for complexing DTPA with super(188)Re from a ready kit and by conventional manipulation were elaborated and the study of the stability and biodistribution of super(188)Re perrhenate and super(188)Re-DTPA were performed. Best labeling was achieved using DTPA (38 mM) with 2 mg/ml of SnCl su...
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Published in: | Journal of radioanalytical and nuclear chemistry 2004-01, Vol.260 (2), p.363-368 |
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container_title | Journal of radioanalytical and nuclear chemistry |
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creator | Faintuch, B L Faintuch, S Muramoto, E |
description | Procedures for complexing DTPA with super(188)Re from a ready kit and by conventional manipulation were elaborated and the study of the stability and biodistribution of super(188)Re perrhenate and super(188)Re-DTPA were performed. Best labeling was achieved using DTPA (38 mM) with 2 mg/ml of SnCl sub(2) super(.)2H sub(2)O. The radiochemical purity was 95.9 plus or minus 2.9%. The complex was stable for 24 hours when ascorbic acid was used. Greatest uptake of super(188)Re-DTPA was by kidneys (19.3 plus or minus 2.1%ID/g) and for super(188)Re-perrhenate by stomach (21.3 plus or minus 2.8%ID/g). In conclusion a kit of freeze-dried DTPA was developed. Organ damage is unlikely by virtue of its rapid urinary excretion. |
doi_str_mv | 10.1023/B:JRNC.0000027110.04651.ec |
format | article |
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title | Preparation and evaluation of two super(188)Re-radiopharmaceuticals for endovascular irradiation |
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