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Journal ArticleDOI

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

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TLDR
The rate and extent of lipid digestion were higher in the emulsion containing liquid particles but that appreciable lipid digestion still occurred in theEmulsion containing solid particles, which may have important consequences for controlling the digestion rate of lipids or for developing solid lipid particle delivery systems for lipophilic functional components.
Abstract
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.

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Citations
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Journal ArticleDOI

Structured emulsion-based delivery systems: controlling the digestion and release of lipophilic food components.

TL;DR: There is a need for edible delivery systems to encapsulate, protect and release bioactive and functional lipophilic constituents within the food and pharmaceutical industries, and emulsion technology is particularly suited for the design and fabrication of delivery systems for lipids.
Journal ArticleDOI

Structuring food emulsions in the gastrointestinal tract to modify lipid digestion.

TL;DR: Greater knowledge and understanding of how the digestive system treats, transports and utilizes lipids will allow the microstructural design of foods to achieve a specific, controlled physiological response.
Journal ArticleDOI

The influence of emulsion structure and stability on lipid digestion

TL;DR: In this paper, food emulsion structure and stability has been investigated in terms of its role in lipid metabolism and metabolism, and it has been shown that food emulsions have a contributing role on lipid digestion and metabolism.
Journal ArticleDOI

Review of in vitro digestion models for rapid screening of emulsion-based systems

TL;DR: The current status of in vitro digestion models for simulating lipid digestion, with special emphasis on the pH stat method, are reviewed, to test the efficacy of different approaches of controlling lipid digestion under conditions that simulate the human gastrointestinal tract.
Journal ArticleDOI

Effect of surfactant surface coverage on formation of solid lipid nanoparticles (SLN).

TL;DR: The results suggest that surfactant coverage at the interface may influence crystal structure and stability of solid lipid nanoparticles via surface-mediated crystal growth.
References
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Journal ArticleDOI

Solid lipid nanoparticles (SLN) for controlled drug delivery - a review of the state of the art.

TL;DR: Relevant issues for the introduction of SLN to the pharmaceutical market, such as status of excipients, toxicity/tolerability aspects and sterilization and long-term stability including industrial large scale production are discussed.
Journal ArticleDOI

Solid lipid nanoparticles: Production, characterization and applications

TL;DR: An overview about the selection of the ingredients, different ways of SLN production and SLN applications, and the in vivo fate of the carrier are presented.
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Solid lipid nanoparticles for parenteral drug delivery.

TL;DR: The biological activity of parenterally applied SLN and biopharmaceutical aspects such as pharmacokinetic profiles as well as toxicity aspects are reviewed.
Journal ArticleDOI

Challenges and solutions for the delivery of biotech drugs--a review of drug nanocrystal technology and lipid nanoparticles.

TL;DR: The use of nanoparticulate carriers, developed in the research group, are described as one solution to overcome drug-associated delivery problems, i.e. drug nanocrystals, solid lipid nanoparticles (SLN), nanostructured lipid carriers (NLC) and lipid-drug conjugate (LDC) nanoparticles.
Journal ArticleDOI

Thermodynamic and kinetic aspects of fat crystallization.

TL;DR: The latest attempts to describe the sometimes complex phase equilibria of fats using fundamental relationships for chemical potential that have so far been applied to individual species in melts of unary, binary and ternary systems are reviewed.
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