Cholesterol as a Subsidiary Component of Sorbitan Surfactant- Based Aggregates: A Study of Formation, Hydrophobicity, and Estimation of Localization of Embedded Molecules

Aggregates of amphiphilic molecules can be used as drug carriers, for which the properties can be modified by mixing with other molecules such as cholesterol. It is important to understand the effects of such additives on the properties because they directly define the material functions. In this work, we investigated the effect of cholesterol on the formation and hydrophobicity of aggregates of sorbitan surfactants. As cholesterol changed its formation from micelles to vesicles, an increase in hydrophobicity was seen, particularly in the middle regions compared with the shallow and deep regions. We show that this gradual hydrophobicity is related to the localization of the embedded molecules. 4-Hydroxy-TEMPO and 4-carboxy-TEMPO were preferentially localized in the shallow region of the aggregates, whereas 4-PhCO2-TEMPO was preferentially localized in the deep region of the vesicle. The localization of molecules depends on their chemical structure. However, the localization of 4-PhCO2- TEMPO in micelles was not observed, despite the similar hydrophobicity in the hydrophobic region within the aggregates. The localization of embedded molecules was related to other properties, such as molecular mobility.

Automated summary

Aggregates of amphiphilic molecules can be used as drug carriers, and their properties can be modified by adding cholesterol. In this study, we investigated the effect of cholesterol on the formation and hydrophobicity of sorbitan surfactant aggregates. Cholesterol changed the formation process from micelles to vesicles and increased the hydrophobicity of the aggregates. The localization of embedded molecules was found to be related to the gradual increase in hydrophobicity.