Hydrophobicity and self‐association (micellization) of bile salts with a lactone or lactam group in a steroid skeleton

다국어 초록 (Multilingual Abstract)

Bile acid salts are amphiphiles that have planar polarity: the convex surface (the β side) of their steroid skeleton is hydrophobic, whereas the concave surface (the α side) is hydrophilic. Lactone and lactam derivatives of bile acid salts have reduced hydrophobicity on the convex surface (β side) of the steroid skeleton, but they are still able to build micelles. In the vicinity of their critical micellar concentration (CMC), they probably form Small's primary micelles. In this work, it is shown that retention capacities (reverse‐phase high‐performance liquid chromatography) are linearly dependent on temperature, for each tested bile acid. The parameters of this linear dependence (intercept and slope) can be used to describe the hydrophobicity of the analyzed bile acid salts. The first and the second principal components, derived from the covariance matrix of temperature dependence of retention capacity, can also be used as hydrophobicity parameters of the analyzed bile acid salts. There is a strong correlation between the CMC values and the values of the hydrophobicity parameters of the convex surface (the β side) of the steroid skeleton: the CMC values decrease as the hydrophobicity of the β side of the steroid skeleton decreases.
Introduction of the lactone or lactam group into the bile acids steroid skeleton (the rings B or C) results in a decrease in the hydrophobicity of the convex surface of the molecule. The matrix of retention parameters at different temperatures, in the set of tested bile acids, can be represented by the values of the principal components. The slope and the interception of linear dependence k = f (T) are also parameters of the hydrophobicity of the bile acids.