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Start date: 2024Subject: search.filters.subject.Emulsion

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    Interfacial composition of coenzyme Q10 emulsions impacts coagulation of fortified milk during gastric digestion
    (Elsevier Ltd, 2025-02-01) Wang X; Zhu P; Ye A; Singh H; Acevedo-Fani A
    This study aimed to investigate the gastric digestion behaviour of heat-treated enriched milk containing Coenzyme Q10-loaded emulsions with different interfacial compositions. Four enriched milk types were compared: pasteurized with a Tween 80 stabilised emulsion (PAST-TW80), or with a sodium caseinate-stabilised emulsion (PAST-NaCN), and UHT with a TW80-stabilised emulsion (UHT-TW80), or PAST with a NaCN-stabilised emulsion (UHT-NaCN); all loaded with Coenzyme Q10. An in vitro dynamic gastric digestion model (Human Gastric Simulator) was utilized and the kinetics of milk coagulation and emptying of protein, lipid and Coenzyme Q10 were monitored. Adding NaCN-stabilised emulsion to heated milk led to a largely fragmented curd with signs of extensive droplets coalescence, disintegrating rapidly and accelerating protein and lipid release. Heated milk with TW80-stabilised emulsion produced a compact and closely integrated curd with limited coalescence, slowing nutrient emptying. UHT milk showed more curd fragmentation than PAST milk, regardless of emulsion type. The release profiles of Coenzyme Q10 were similar between UHT-TW80 and PAST-TW80 or between PAST-NaCN and UHT-NaCN, indicating the emulsion's interfacial composition as a key factor in controlling lipophilic bioactive release from the food matrix, regardless of heat treatment. These findings demonstrate that the emulsion's interfacial composition (NaCN vs TW80) and the heat treatment (PAST vs UHT) can be combined as a strategy to modulate milk coagulation kinetics and the rate of nutrient delivery to the small intestinal stage. This study provides insights into the development of functional milk products fortified with lipophilic bioactive compounds, as well as strategies for optimizing the controlled release of these compounds upon consumption.
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    The physicochemical properties of β-carotene emulsions stabilized by whey protein/octenyl succinic anhydride (OSA)-modified-starch complexes: Influence of OSA substitution degree of starch
    (Elsevier Ltd, 2024-04-01) Lin Q; Yang X; Liu Y; Lu Y; Liu W; Han J; Singh H; Ye A
    Complexes formed between heated whey protein isolate (HWPI) and octenyl succinic anhydride (OSA)-modified starches were prepared to stabilize β-carotene-containing oil-in-water emulsions. The zeta-potential, turbidity, particle size, and microstructure of the complexes were determined to evaluate the impact of the degree of substitution (DS) of OSA-modified starch on the complexes' structure. HWPI and OSA-modified starches with low DS values formed elongated complexes. With increasing DS, the particle size of the complexes reduced. In comparison to the emulsions stabilized by HWPI or OSA-modified starches, the emulsions stabilized by HWPI/OSAS complexes exhibited superior protection of β-carotene during storage under acidic conditions. When the DS of OSA-modified starch increased, the particle size of emulsions stabilized by the complexes decreased, with less droplet aggregation occurring. The physical stability of these emulsions against storage time, ions, and thermal process showed a positive relationship with the DS, while the β-carotene retention in the emulsions during storage showed a negative relationship with the DS. The greater physical stability of the complex-stabilized emulsions containing OSA-modified starch with a higher DS may be ascribed to enhanced electrostatic repulsion among oil droplets and the formation of a more rigid and denser surface structure in the presence of more OSA groups.