Abstract
Summary and conclusions
(1) Doses of 0.05 mc of Y90Cl3 solution and of CrP32O4 colloidal suspension in 0.05 or 0.1 ml were injected into ventral surface of tails in mice. At intervals of 1 minute to 3 days after injection, tails were serially amputated and preserved until 3rd day when every mouse was sacrificed; their organs (liver, lung, spleen, kidney), tails and heart blood (0.3 ml) were emulsified, dried and tested for radioactivity content with a Geiger Tube Detector. (2) Results showed only a narrow range of radioactivity for each organ specimen calculated as a product of the average blood radioactivity in the same group of mice (amputated at the same time). (3) The calculated and tabulated data show that a significant proportion of CrP32O4 was translocated into the liver from the tail; for Y90 the initial storage in the tail was very high, but some translocation occurred, presumably by excretion. (4) The pattern of Y90 and CrP32O4 distribution in the body after injection into the tail was comparable to delayed results of intravenous injection; this resemblance was interpreted by high vascularization of the tail. (5) It was concluded that the method of serial tail amputation may be useful for outlining the dynamics of isotopes spread in bodies of experimental animals.
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