Department of Food and Nutrition, University of Helsinki, P.O. Box 66, FI-00014 Helsinki, Finland; Faculty of Agriculture and Forestry, Helsinki Institute of Sustainability Science, University of Helsinki, 00014 Helsinki, Finland.
Department of Food and Nutrition, University of Helsinki, P.O. Box 66, FI-00014 Helsinki, Finland.
Food Res Int. 2022 Oct;160:111633. doi: 10.1016/j.foodres.2022.111633. Epub 2022 Jul 8.
The interest on the digestive fate of oleogels, i.e., substitutes for solid fats rich in liquid oil, have pushed researchers to use the widely adopted INFOGEST protocol for static in vitro digestion. However, this protocol was originally designed to simulate the digestibility of conventional foods and to accommodate the large fraction of oil in oleogels, researchers have deliberately modified the INFOGEST protocol, inadvertently leading to results difficult to be compared. In this study, we highlighted possible problems that may arise during oleogel simulated digestion such as under- or overestimation of oleogel lipolysis. The effect of oleogel amount, oleogelator type and concentration, and shear applied during digestion on the rate and extent of oleogel digestion was studied. The release of fatty acids during the application of INFOGEST protocol was monitored using the pH-stat method and compared to those analyzed by HPLC-ELSD. Oleogels' structural information was obtained using brightfield, polarized, and fluorescence microscopy, and DSC. We determined that lipolysis of ethylcellulose oleogels follow the "interaction with enzymes and bile salts" pattern, whereas that of wax oleogels follow the "disintegration of oleogel and interaction with enzymes and bile salts". We also observed that the chemical composition of wax, crystal morphology, and crystal distribution do not alter the lipolysis of oil entrapped inside the wax crystals. We finally recommended a few minimal but fundamental modifications to the INFOGEST protocol to achieve more reliable results from the static in vitro digestion of oleogels and possibly other lipid-based systems.
人们对油凝胶(富含液体油的固体脂肪替代品)消化命运的兴趣促使研究人员使用广泛采用的 INFOGEST 协议进行静态体外消化。然而,该协议最初是为模拟常规食品的消化率而设计的,并且要适应油凝胶中大量的油分,因此研究人员故意修改了 INFOGEST 协议,无意中导致结果难以比较。在本研究中,我们强调了在模拟油凝胶消化过程中可能出现的问题,例如对油凝胶脂解的低估或高估。研究了油凝胶量、凝胶剂类型和浓度以及消化过程中施加的剪切力对油凝胶消化速率和程度的影响。使用 pH -stat 法监测 INFOGEST 协议应用过程中脂肪酸的释放,并与通过 HPLC-ELSD 分析的脂肪酸释放进行比较。使用明场、偏光和荧光显微镜以及差示扫描量热法(DSC)获得油凝胶的结构信息。我们确定了乙基纤维素油凝胶的脂解遵循“与酶和胆汁盐相互作用”的模式,而蜡质油凝胶的脂解遵循“油凝胶的崩解和与酶及胆汁盐相互作用”的模式。我们还观察到蜡的化学组成、晶体形态和晶体分布不会改变包裹在蜡晶体内部的油的脂解。我们最后建议对 INFOGEST 协议进行一些最小但基本的修改,以从油凝胶和可能其他基于脂质的系统的静态体外消化中获得更可靠的结果。