1990
DOI: 10.1007/bf00649450
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Calorimetric study of the solubilization of cholesterol, retinol and retinal by reversed AOT micelles

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Cited by 10 publications
(6 citation statements)
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“…Thus, knowledge of the interactions that are involved in their solubilization in reverse micelles and their dependence on functional groups that may be present in the molecule could help in understanding the analogous processes in biological membranes. D'Aprano et al (22) have studied the solubilization of retinol and retinal in n-heptane/AOT/water reverse micelles by calorimetric methods and suggested that the interactions between the double C=C bonds with the hydrophilic regions of the AOT determine their behavior. Recently it has been reported (23) that carotenoids can act as end-cap-active agents in lecithin cylindrical micelles in diverse organic solvents, but some questions still remain about the mechanism and influence of substituents in this behavior.…”
Section: Methodsmentioning
confidence: 99%
“…Thus, knowledge of the interactions that are involved in their solubilization in reverse micelles and their dependence on functional groups that may be present in the molecule could help in understanding the analogous processes in biological membranes. D'Aprano et al (22) have studied the solubilization of retinol and retinal in n-heptane/AOT/water reverse micelles by calorimetric methods and suggested that the interactions between the double C=C bonds with the hydrophilic regions of the AOT determine their behavior. Recently it has been reported (23) that carotenoids can act as end-cap-active agents in lecithin cylindrical micelles in diverse organic solvents, but some questions still remain about the mechanism and influence of substituents in this behavior.…”
Section: Methodsmentioning
confidence: 99%
“…It had been shown [25] that cholesterol is preferentially solubilised in the palisade layer contrary to retinol and retinal, which prefer the aqueous microphase. Comparing structures of the α-tocopherol molecule to cholesterol, retinol and retinal (Scheme 1) we suppose that α-tocopherol molecules are preferentially located in the palisade layer of the AOT reversed micelles similarly to cholesterol.…”
Section: Resultsmentioning
confidence: 97%
“…Actually we can deduce the α-tocopherol favourable sites in AOT reversed micelles indirectly. In Table 1 the thermodynamic parameters for α-tocopherol transfer from the n-heptane to AOT reversed micelles have been compared with D'Aprano values reported for cholesterol, retinal and retinol at R = 0 and at the same temperature [25].…”
Section: Resultsmentioning
confidence: 99%
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“…Recent studies about volumetric properties of these pentanols with toluene [1], viscometric and thermodynamic properties of pentanols þ n-heptane [2,3] carried out in our laboratory are considered as highly relevant to the present work. Other works of sufficient interest in relation to the present one are those of D'Aprano [4][5][6][7][8]. We report here the viscosity and relevant thermodynamic activation parameters for the binary mixtures of 1-pentanol, 2-pentanol and 3-pentanol with toluene, which as far as we know, are not available in literature.…”
Section: Introductionmentioning
confidence: 90%