Hydrophobicity and self-association (micellisation) of bile salts with a lactone or lactam group in a steroid skeleton
| Autor: | Ksenija Pavlović, Ljubica Grbović, Mihalj Poša, Vesna Tepavčević, Mira Mikulic |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
chemistry.chemical_classification
010405 organic chemistry Stereochemistry medicine.medical_treatment Self association Organic Chemistry 010402 general chemistry 01 natural sciences Skeleton (computer programming) 0104 chemical sciences Steroid chemistry.chemical_compound chemistry Principal component method Group (periodic table) medicine Lactam Physical and Theoretical Chemistry Lactone |
| Zdroj: | Journal of Physical Organic Chemistry. 34(2) |
| ISSN: | 0894-3230 |
| Popis: | 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. © 2020 John Wiley & Sons, Ltd. |
| Databáze: | OpenAIRE |
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