Rate-of-dialysis technique: theoretical and practical aspects

In the rate-of-dialysis technique, chemical equilibrium exists throughout the experiment between the contents of the two halves of a dialysis cell. Initially, however, a trace amount of labeled dialysand is present in one of the half-cells, and the dialysis of that is followed as a function of time. The method is able to reveal whether a compound is stable under the conditions used or whether it is affected, for example, by aggregation, precipitation, oxidation, or hydrolysis. The rate constants for six inorganic ions and 22 organic molecules were determined, and no simple relations were found between rate constants and functions of molar masses. However, in two homologous series of compounds, a linear relationship between rate constant and molar mass was found, allowing for a preliminary identification of an unknown substance. Whether the presence of a macromolecule results in binding of the dialysand is easily tested for because in that case its rate constant is sharply diminished. High-affinity binding was studied using octanoate and laurate as ligands and human serum albumin as binding protein. The primary binding constants determined were similar to those obtained by equilibrium dialysis. However, the rate-of-dialysis technique is much faster, and its results are less scattered. The technique is well suited for binding studies performed with high protein concentrations because it is not affected by any osmosis or Donnan effects.