Tailoring Emulsions for Controlled Lipid Release: Establishing in vitro-in Vivo Correlation for Digestion of Lipids

被引:70
作者
Scheuble, Nathalie [1 ]
Schaffner, Joschka [1 ]
Schumacher, Manuel [1 ]
Windhab, Erich J. [1 ]
Liu, Dian [2 ,3 ]
Parker, Helen [4 ,5 ]
Steingoetter, Andreas [2 ,3 ,4 ]
Fischer, Peter [1 ]
机构
[1] ETH, Inst Food Nutr & Hlth, CH-8092 Zurich, Switzerland
[2] Univ Zurich, Inst Biomed Engn, CH-8092 Zurich, Switzerland
[3] ETH, CH-8092 Zurich, Switzerland
[4] Univ Hosp Zurich, Div Gastroenterol & Hepatol, CH-8091 Zurich, Switzerland
[5] Newcastle Univ, Inst Hlth & Soc, Newcastle Upon Tyne, Tyne & Wear, England
基金
瑞士国家科学基金会;
关键词
lipid digestion; gastric digestion; intestine digestion; interfacial design; human studies; in vitro-in vivo correlation; HUMAN GASTRIC LIPASE; INTRAGASTRIC ACID STABILITY; HEALTHY-SUBJECTS; INTESTINAL LIPOLYSIS; CRYSTAL-STRUCTURE; CELLULOSE; FOOD; ADSORPTION; INTERFACES; MUCIN;
D O I
10.1021/acsami.8b02637
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The use of oil-in-water emulsions for controlled lipid release is of interest to the pharmaceutical industry in the development of poorly water soluble drugs and also has gained major interest in the treatment of obesity. In this study, we focus on the relevant in vitro parameters reflecting gastric and Stomach intestinal digestion steps to reach a reliable in vitro-in vivo correlation for lipid delivery systems. We found that (i) gastric lipolysis determines early lipid release and sensing. This was mainly influenced by the emulsion stabilization mechanism. (ii) Gastric mucin influences the structure of charge-stabilized emulsion systems in the stomach, leading to destabilization or gel formation, which is supported by in vivo magnetic resonance imaging in healthy volunteers. (iii) The precursor structures of these emulsions modulate intestinal lipolysis kinetics in vitro, which is reflected in plasma triglyceride and cholecystokinin concentrations in vivo.
引用
收藏
页码:17571 / 17581
页数:11
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