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Evaluation of the lipophilicity of selected sunscreens—A chemometric analysis of thin‐layer chromatographic retention data
Author(s) -
Sobanska Anna W.,
Wójcicka Kamila,
Brzezinska Elżbieta
Publication year - 2014
Publication title -
journal of separation science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.72
H-Index - 102
eISSN - 1615-9314
pISSN - 1615-9306
DOI - 10.1002/jssc.201400535
Subject(s) - lipophilicity , chemistry , chromatography , partition coefficient , octanol , thin layer chromatography , acetone , chemometrics , tetrahydrofuran , methanol , solvent , organic chemistry
The lipophilicities of 22 selected sunscreens, preservatives, and vitamins used in topical skin products were measured by thin‐layer chromatography. Lipophilicity was calculated in silico from the sunscreen molecular structures and compared to the experimental octanol/water partition coefficients found in the literature. The retention of the compounds was investigated on an RP‐18 stationary phase with mobile phases consisting of water and one of six organic modifiers (dioxane, tetrahydrofuran, acetone, acetonitrile, methanol, and dimethylformamide) at different concentrations. The theoretical lipophilicities were calculated by several computational algorithms and the results of these calculations were compared using cluster analysis. The results showed that two out of the six investigated organic modifiers (dioxane and acetone) may be used to estimate the octanol/water partition coefficients of highly lipophilic compounds having lipophilicities that cannot be measured directly by the shake‐flask method.