4.7 Article

Lutein-enriched emulsion-based delivery systems: Impact of Maillard conjugation on physicochemical stability and gastrointestinal fate

Journal

FOOD HYDROCOLLOIDS
Volume 60, Issue -, Pages 38-49

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.foodhyd.2016.03.021

Keywords

Lutein; Storage stability; Casein; Dextran; Maillard conjugates; In vitro digestion

Funding

  1. Agriculture and Food Research Initiative from the USDA National Institute of Food and Agriculture [2014-67017-21635]
  2. Ministry of National Education of Turkey
  3. NIFA [687468, 2014-67017-21635] Funding Source: Federal RePORTER

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The utilization of lutein as a natural colorant or nutraceutical in many foods, supplements, and other commercial products is currently limited because of its low water-solubility and chemical instability. The purpose of this study was to evaluate the effect of Maillard conjugates on the physical and chemical stability of lutein-enriched emulsions exposed to different temperatures and pH values, as well as on their potential gastrointestinal fate. Oil-in-water emulsions were prepared using either casein or caseindextran conjugates as emulsifiers. Both types of emulsions showed a slight increase in particle aggregation at temperatures exceeding 37 degrees C, and became more prone to color fading (lutein degradation) as the temperature was increased. Casein-coated oil droplets were highly unstable to flocculation near their isoelectric point (pH 4-5) due to the reduction in electrostatic repulsion. However, casein-dextrancoated droplets were stable from pH 3 to 7, which was attributed to strong steric repulsion by the dextran moiety. The casein-coated droplets were unstable to aggregation in the gastric phase of the simulated GIT, whereas the casein-dextrin-coated ones were stable, which was again attributed to increased steric repulsion. Emulsifier type did not strongly influence lutein bioaccessibility. This work shows that Maillard conjugates can improve the physical stability of lutein-enriched emulsions without adversely affecting the bioaccessibility of the bioactive agent. (C) 2016 Elsevier Ltd. All rights reserved.

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