4.7 Article

Modification of the interfacial structure of droplet-stabilised emulsions during in vitro dynamic gastric digestion: Impact on in vitro intestinal lipid digestion

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 608, Issue -, Pages 1286-1296

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.10.075

Keywords

Droplet-stabilised emulsion; Interfacial structure; Calcium caseinate particles; In vitro dynamic gastric digestion; In vitro small intestinal digestion

Funding

  1. Riddet Institute, a National Centre of Research Excellence (CoRE)
  2. New Zealand Tertiary Education Commission

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The study found that during in-vitro digestion, the droplet size of a nano-sized droplet-stabilised emulsion increased after gastric digestion, leading to a slightly higher release of free fatty acids compared to a control emulsion. The release rate of free fatty acids in the small intestine was higher for the droplet-stabilised emulsion compared to the control during the initial 30 minutes, with similar release rates observed beyond 30 minutes.
The in-vitro gastrointestinal digestion behaviour of an oil-in-water emulsion with an interface consisting of nano-sized droplets coated with caseinate particles, referred to as a droplet-stabilised emulsion (DSE), was explored using the human gastric simulator and pH-stat models. A caseinate-particle-stabilised emulsion (PSE) was used as a control, with a similar droplet size distribution and the same composition as the DSE. The nanodroplet-stabilised interface of the DSE was preserved during the first 180 min of gastric digestion. During 240 min, the droplet sizes of the DSE and the PSE increased from 22.71 +/- 1.14 to 63. 34 +/- 6.57 lm and from 17.98 +/- 1.16 to 85.11 +/- 9.35 lm respectively. The small droplet size of the DSE that was released from the gastric phase contributed to slightly higher total free fatty acid (FFA) release (56. 18 +/- 3.55%) than that from the PSE (49.4 +/- 2.67%). The FFA release rate of the DSE (1.21 % min-1) was greater than that of the PSE (1.06 % min-1) during the first 30 min of small intestinal digestion; similar FFA release rates (0.5 mmol s-1 m-2 x 10-4) were obtained for both emulsions beyond 30 min of diges

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