Self-diffusion nuclear magnetic resonance, microstructure transitions, and solubilization capacity of phytosterols and cholesterol in Winsor IV food-grade microemulsions

Aviram Spernath, Anan Yaghmur, Abraham Aserin, Roy E Hoffman, Nissim Garti

    61 Citations (Scopus)

    Abstract

    Microemulsions are of growing interest to the food industry as vehicles for delivering and enhancing solubilization of natural food supplements with nutritional and health benefits. The incorporation of molecular phytosterols, cholesterol-lowering agents, in food products is of great interest to the food industry. In this work is demonstrated the use of water dilutable food-grade microemulsions consisting of ethoxylated sorbitan ester (Tween 60), water, R-(+)-limonene, ethanol, and propylene glycol as vehicles for enhancing the phytosterols solubilization. Phytosterols were solubilized up to 12 times more than the dissolution capacity of the oil [R-(+)-limonene] for the same compounds. The solubilization capacity of phytosterols and cholesterol along a dilution line in a pseudo-ternary phase diagram [on this dilution line the weight ratio of R-(+)-limonene/ethanol/Tween 60 is constant at 1:1:3] was correlated to the microstructure transitions along the dilution line. Structural aspects were studied by self-diffusion NMR spectroscopy. The ability of phytosterols to compete with cholesterol for penetration into bile salt micelles in the gut may be limited to rich aqueous systems (O/W microemulsion).
    Original languageEnglish
    JournalJournal of Agricultural and Food Chemistry
    Volume51
    Issue number8
    Pages (from-to)2359-64
    Number of pages6
    ISSN0021-8561
    DOIs
    Publication statusPublished - 9 Apr 2003

    Keywords

    • Cholesterol
    • Cyclohexenes
    • Diffusion
    • Emulsions
    • Ethanol
    • Food Technology
    • Magnetic Resonance Spectroscopy
    • Phytosterols
    • Solubility
    • Solutions
    • Surface-Active Agents
    • Terpenes

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