2011
DOI: 10.1016/j.cis.2011.02.001
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Behaviour of protein-stabilised emulsions under various physiological conditions

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Cited by 238 publications
(152 citation statements)
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“…During the digestion, lipid is broken down into oil-in-water (o/w) emulsions due to the mechanical stresses, the influence of surface-active and stabilizing components, and then its chemistry and structural organization will be changed [5][6][7]. Hence, the initial emulsion form of the lipid phase in food may impact its subsequent absorption and digestion [8,9].…”
Section: Introductionmentioning
confidence: 99%
“…During the digestion, lipid is broken down into oil-in-water (o/w) emulsions due to the mechanical stresses, the influence of surface-active and stabilizing components, and then its chemistry and structural organization will be changed [5][6][7]. Hence, the initial emulsion form of the lipid phase in food may impact its subsequent absorption and digestion [8,9].…”
Section: Introductionmentioning
confidence: 99%
“…In particular, since lipid digestion is an interfacial process, largely controlled by the binding of lipase-colipase complex onto the surface of emulsified droplets, it seems possible to alter the kinetics and degree of lipid digestion by modification of the interfacial structures or controlling the transport of lipase [13][14][15] , and in turn to potentially control satiety. However, in most surfactant-and protein-stabilized emulsions, the adsorbed layers are displaced by biosurfactants, in particular bile salts [16][17][18][19][20] . Thus, the interfacial structure of the initial emulsion is not necessarily retained in the physiological regime, to allow easy adsorption of the lipase-colipase complex to the bile adsorbed surface and thus enable lipolysis and release of fatty acids.…”
Section: Introductionmentioning
confidence: 99%
“…shear and temperature) and biochemical (e.g. dilution, ionic strength, 515 pH, pepsin, amylase, pancreatin, mucins and bile salts) conditions as it passes through the 516 mouth into the stomach and then the intestines (Singh & Sarkar, 2011). During its 517 physiological transit, the emulsion microgel particle can release the encapsulated active 518 molecule by two approaches: 1.…”
mentioning
confidence: 99%