Issue 11, 2004

Transitions and loci of solubilization of nutraceuticals in U-type nonionic microemulsions studied by self-diffusion NMR

Abstract

U-type microemulsions based on five food-grade ingredients, water, R(+)-limonene, ethanol, propylene glycol, (or glycerol) and ethoxylated sorbitan esters (Tween 60 or Tween 80) were studied. The U-type phase diagram is characterized by a unique composition, fully dilutable with the aqueous phase that inverts progressively from an L2 phase to an L1 phase via a bicontinuous structure without phase separation. The ‘oil concentrate’ (surfactant, oil, alcohol) is loaded with water-insoluble solubilizates (phytosterols, lutein and lycopene) a few times more than the solubility capacity of the oil phase (without the surfactant). The maximum solubilization capacity (μ-value) was obtained for phytosterols and the minimum solubilization capacity was for lycopene. All solubilization values decrease with aqueous phase dilution. If solubilization is calculated on the basis of the oil content (α-value) or the oil + surfactant (γ-value) it is obvious that the interface plays a key role in the solubilization.The lipophilic solubilizates (by SD-NMR) are tightly packed and well accommodated at interfaces that convex (hydrophobic-in-nature) toward the water (water-in-oil microemulsions). Solubilization at the bicontinuous interface is lower and the solubilizates are loose packed. Once phase inversion occurs, and the interface becomes more hydrophilic and transforms into oil-in-water microemulsion, the solubilization becomes minimal, and most of the solubilizate desorbs. Phytosterols and lycopene induce the transition from W/O to bicontinuous and it occurs at lower water content (ca. 25 wt% aqueous phase in the presence of solubilizate vs. 35 wt% in its absence). The transition from bicontinuous to O/W is mostly unaffected (or undetected) since the interface flattens out and the solubilizate does not affect the curvature much. Lutein displays different behavior, the transition, from bicontinuous phase to O/W, occurs at higher water contents because its adsorption and packing are significantly tighter. Solubilization capacities of each of the nutraceuticals were determined for all dilution compositions.

Article information

Article type
Paper
Submitted
22 Mar 2004
Accepted
13 Apr 2004
First published
12 May 2004

Phys. Chem. Chem. Phys., 2004,6, 2968-2976

Transitions and loci of solubilization of nutraceuticals in U-type nonionic microemulsions studied by self-diffusion NMR

N. Garti, I. Amar-Yuli, A. Spernath and R. E. Hoffman, Phys. Chem. Chem. Phys., 2004, 6, 2968 DOI: 10.1039/B404315B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements