The formation mechanism of multilayer emulsions studied by isothermal titration calorimetry and dynamic light scattering

被引:6
作者
Liao, Wei [1 ]
Dumas, Emilie [1 ]
Elaissari, Abdelhamid [2 ]
Gharsallaoui, Adem [1 ]
机构
[1] Univ Claude Bernard Lyon 1, Univ Lyon, CNRS, LAGEPP UMR 5007, 43 Bd 11 Novembre 1918, F-69622 Villeurbanne, France
[2] Univ Claude Bernard Lyon 1, Univ Lyon, CNRS, ISA UMR 5280, F-69622 Villeurbanne, France
关键词
Multilayer emulsions; Isothermal titration calorimetry; Dynamic light scattering; Electrostatic interactions; Bridging flocculation; COMPLEX COACERVATION; SODIUM-CASEINATE; PROTEIN ISOLATE; O/W EMULSIONS; STABILITY; CHITOSAN; ADSORPTION; BEHAVIOR; POLYSACCHARIDES; FLOCCULATION;
D O I
10.1016/j.foodhyd.2022.108275
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The formation of multilayer interfaces in oil-in-water (O/W) systems has many advantages in delivering lipid -soluble active compounds. In this study, isothermal titration calorimetry (ITC) and dynamic light scattering (DLS) were used to investigate the formation mechanism of multilayer emulsions by mixing low methoxyl pectin (LMP) and sodium caseinate (CAS) stabilized O/W emulsion. Thermodynamic properties and zeta-potential curves were studied as a function of polymer ratio, suggesting that ITC could provide more accurate information about the polymer concentration effect. ITC titration confirmed that LMP binds CAS-coated droplets mainly through electrostatic forces, which was a spontaneous exothermic process (Delta G < 0). Furthermore, stable multilayer emulsions were obtained by titrating CAS-stabilized droplets into LMP instead of back-titrating. Finally, the effects of mixing methods on the stability of multilayer emulsions were evaluated. The results suggest that titration rather than direct mixing can produce uniform and smaller-sized droplets and delay the onset of droplets aggregation.
引用
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页数:11
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