The availability of radioactive isotopes of iron led to the development of reliable methods of studying iron kinetics (1), but the absorption of iron by the gastrointestinal tract was still determined indirectly by the amount of unabsorbed iron excreted in the stools or by quantification of isotopic iron incorporated into hemoglobin (2-7). The availability of a whole-body counter in a clinical facility has made possible the direct assay of iron59 retention in human subjects and has eliminated sample collecting and preparation. The purpose of this paper is to describe this method and demonstrate some of the findings.
METHODS AND MATERIALSThirty-five volunteers, 25 normal and 10 iron-deficient adults, were the subj ects of the study. The iron-deficient subjects met one or more of the following criteria: 1) virtual absence of iron in bone marrow smears stained by the Prussian-blue reaction (8) ; 2) serum iron less than 70 Ag per 100 ml with total iron-binding capacity in excess of 350 jig (9, 10) ; 3) recent loss of blood without replacement by iron or transfusion. Five subjects (Tables IV and V, numbers 1, 3, 4, 7 and 9) had been purposely phlebotomized to induce iron deficiency. They were in various stages of recovery following the loss of 4 or 5 units (2.0 to 2.5 L) of blood in a period of 1 month. In Subjects 4 and 9 the peripheral parameters had become normal at a time when one could be sure from the history, amount of blood loss and the lack of iron in the marrow, that the body iron stores had not been replenished.The normal iron-replete subj ects met none of these criteria. Serum iron was in excess of 80 ,ug per 100 ml; there was no evidence of bleeding or history of recent blood loss. Red cell indices were established in all subjects. None of the subjects was known to have neoplastic, infectious or inflammatory disease.Iron absorption studies were performed in each subject with radioactive iron' and a whole-body liquid scintillation counter. The instrument was a 47r liquid scintillation counter simliar in design to the Los Alamos counter (11). The major differences were an increase in diameter of the sample well to 20 inches and the substitution of thirty 5-inch photocathode tubes. This instrument was operated as a two-channel analyzer, specifically to detect body cesium.. and potassium' with maximal efficiency. The two ranges of -y-energy discrimination were wide (0.3 to 0.8 and 0.8 to 2.0 Mev) and useful for detecting a large number of y-emitting nuclides with good efficiency.The standards used were a 2.5 L water-filled plastic bottle to which iron" was added in amounts equal to half the dose given the subject. A 250 ml plastic bottle similarly prepared was used as a standard for measurement of radioactivity in feces.Prior to administration of the radionuclide, the volunteers were assayed in the body counter. They lay supine on a canvas sling within the sample chamber (Figure 1).