Measuring microscopic hormones in human blood was once like trying to find a single grain of sand on a vast beach; Rosalyn Yalow and Solomon Berson used radioactive isotope tags to measure microscopic hormone molecules at parts-per-trillion sensitivity. Awarded the 1977 Nobel Prize in Medicine, Radioimmunoassay founded modern endocrinology and is the analytical foundation behind blood bank screening, thyroid testing, and home pregnancy kits worldwide.

In mid-twentieth-century medicine, doctors were blind to the endocrine system: vital hormones like insulin, thyroid hormones, and human growth hormones exist in human blood at microscopic concentrations—equivalent to a single drop of water in an Olympic swimming pool. Scientists had no physical lab test sensitive enough to measure them.
Medical physicist Rosalyn Yalow designed an atomic scale using radioactive isotopes. In a game of microscopic musical chairs, radioactive hormone tags compete with natural hormones in a patient’s blood to bind to specific antibodies—allowing a simple radiation counter to measure exact hormone concentrations in minutes.
Yalow became the second woman in history to win the Nobel Prize in Medicine. By proving that Type 2 diabetes is caused by insulin resistance rather than a lack of insulin, by securing the global blood supply against hepatitis and HIV, and by enabling modern diagnostic medicine, RIA transformed healthcare.
IMMUNOASSAY OF ENDOGENOUS PLASMA INSULIN IN MAN
For years investigators have sought an assay for insulin which would combine virtually absolute specificity with a high degree of sensitivity, sufficiently exquisite for measurement of the minute insulin concentrations usually present in the circulation. Methods in use recently depend on the ability of insulin to exert an effect on the metabolism of glucose in vivo or in excised muscle or adipose tissue. Thus, the insulin concentration in plasma has been estimated: a) from the degree of hypoglycemia produced in hypophysectomized, adrenalectomized, alloxan-diabetic rats (1); b) from the augmentation of glucose uptake by isolated rat hemidiaphragm (2); or c) from the increased oxidation of glucose-1-C14 by the rat epididymal fat pad (3). Since there have been reports indicating the presence, in plasma, of inhibitors of insulin action (4) and of noninsulin substances capable of inducing an insulin-like effect (5,6), these procedures, while yielding interesting information regarding the effects of various plasmas on glucose metabolism in tissues, are of doubtful specificity for the measurement of insulin per se (5).
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