Abstract
The simultaneous administration of carrier gallium has been shown [1] to change the biodistribution of carrier-free 67Ga from one of predominately soft-tissue distribution to localization primarily in bone and kidney. In tumor-bearing animals, administration of carrier gallium significantly reduced 67Ga accumulation in tumor tissue [2]. There is little available data concerning the effect of carrier on the tissue distribution and tumor localization of 67Ga. when the interval between the injection of carrier and tracer is varied. Conceivably, carrier material appropriately administered might offer a useful means of affecting tracer distribution in a tumor-bearing host and enhance the lesion-background ratios of tumor-seeking radiopharmaceuticals. We explored this question for both Ga/67Ga (a trace metal with no known intracellular function) [3] and Mn/54Mn, and ion known to enter mitrochondia [4] and intimately associated with cellular metabolism [5]. Since both of these metals develop high tumor-background ratios [3,6], have positron-emitting isotopes suitable for use with the newer positron-imaging devices, and have been shown to alter tumor growth rates [7–9], these data might be useful for both diagnosis and therapy.
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Halpern, S.E., Hagan, P. (1980). Effect of Carrier on the Distribution of 54Mn and 67Ga in Tumor-Bearing Animals. In: Horst, W., Wagner, H.N., Buchanan, J.W. (eds) Frontiers in Nuclear Medicine. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-67575-1_15
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DOI: https://doi.org/10.1007/978-3-642-67575-1_15
Publisher Name: Springer, Berlin, Heidelberg
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