6533b7dbfe1ef96bd126f770

RESEARCH PRODUCT

Influence of lipid physical state on the in vitro digestibility of emulsified lipids.

Sandra SandraLucile BonnaireDavid Julian McclementsThrandur HelgasonEric A. DeckerJochen Weiss

subject

Chemical PhenomenaSwineFatty Acids NonesterifiedIn Vitro Techniqueschemistry.chemical_compoundAnimalsLipaseSodium dodecyl sulfateParticle SizeChromatographybiologyChemistry PhysicalLipid metabolismGeneral ChemistryLipaseLipid MetabolismLipidschemistryEmulsionTripalmitinbiology.proteinDigestionEmulsionsLipid particleParticle sizeGeneral Agricultural and Biological SciencesLipid digestion

description

The objective of this study was to investigate the influence of the physical state of emulsified lipids on their in vitro digestibility by pancreatic lipase. A 10 wt % tripalmitin oil-in-water emulsion stabilized by sodium dodecyl sulfate (0.9 wt % SDS) was prepared at a temperature (>70 degrees C) above the melting point of the lipid phase (T(m) approximately 60 degrees C). A portion of this emulsion was cooled to a temperature (0 degrees C for 15 min) well below the crystallization temperature of the emulsified lipid (T(c) approximately 22 degrees C) and then warmed to 37 degrees C so as to have completely solid lipid particles. Another portion of the emulsion was directly cooled from 70 to 37 degrees C (which is above the T(c)) to have completely liquid (supercooled) lipid particles. Pancreatic lipase (8 mg/mL) and bile extract (5.0 mg/mL) were then added to each emulsion at 37 degrees C, and the evolution of the particle charge, particle size, appearance, and free fatty acid release were measured over a period of 2 h. It was found that the rate and extent of lipid digestion were higher in the emulsion containing liquid particles but that appreciable lipid digestion still occurred in the emulsion containing solid particles (i.e., >35% lipid digestion after 2 h). These results may have important consequences for controlling the digestion rate of lipids or for developing solid lipid particle delivery systems for lipophilic functional components.

10.1021/jf800159ehttps://pubmed.ncbi.nlm.nih.gov/18433107