Abstract
Thirteen simultaneous measurements were made with T-1824 and an improved I131-albumin method in 12 subjects. Significant loss of labeled protein to glassware was prevented by addition of homologous plasma to the I131-albumin used for injection and preparation of standards and by using physiological saline containing carrier protein (2 ml plasma/100 ml) as diluent for the standards. In this series the I131-albumin dilution spaces averaged +5.3% higher than the dye dilution spaces. At the time of each measurement the proportion of loosely bound I131 was also determined by precipitating the labeled protein with trichloroacetic acid and measuring the radioactivity in the supernatant. In different samples it varied from 2.1 to 4.8% of the total. If correction is made for the loosely bound I131, a large part of which was shown to be removed quickly from the circulation, the average difference is reduced to +1.2% (S.D. 3.0%). These findings indicate that, when the above precautions are taken, the I131-albumin method gives measurements in close agreement with measurements by the dye method. Submitted on March 17, 1958