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首页> 外文期刊>Food research international >In vitro digestion of foods using pH-stat and the INFOGEST protocol: Impact of matrix structure on digestion kinetics of macronutrients, proteins and lipids
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In vitro digestion of foods using pH-stat and the INFOGEST protocol: Impact of matrix structure on digestion kinetics of macronutrients, proteins and lipids

机译:使用pH-stat和INFOGEST方案进行食品的体外消化:基质结构对大量营养素,蛋白质和脂质消化动力学的影响

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It is currently admitted that food structure can facilitate or delay the release of nutrients during digestion and their absorption by the human body. The aim of this study is to propose an in vitro method able to assess the behavior of lipo-proteinic matrices with different structures during digestion. Two model matrices of exactly the same compositions (10% oil, 15% whey proteins, w/w) were designed: i) A liquid emulsion (LE) made of small fat droplets (1 mu m) dispersed in a liquid continuous phase containing native whey proteins, ii) a solid emulsion (SE) made of a continuous whey protein gel entrapping large oil droplets (20 mu m). The two matrices were digested through an in vitro gastro-intestinal protocol based on the INFOGEST guidelines using pH-stat to monitor the enzymatic hydrolyses of both proteins and lipids. By further digesting lipid-free matrices in the same conditions, the contributions of the proteolytic and lipolytic reactions were evaluated. Significant differences were observed between matrices at both short and long digestion times. The initial rates of both proteolysis andlipolysis were slower for SE than LE because of the gel state of the continuous phase. At the end of the experiments, SE led to a smaller extent of lipolysis (DHlip_SE = 51% < DHlip_LE = 81%) but a greater extent of proteolysis (DHprot_SE = 80% > DHprot_LE = 52%) because of the higher sensitivity to digestion of denatured whey proteins. These results highlight the impact of matrix structure on enzyme accessibility, and show that the proposed method is suitable to monitor the digestion of complex food matrices. (C) 2015 Elsevier Ltd. All rights reserved.
机译:目前公认,食物结构可以促进或延迟营养在人体消化过程中的释放以及被人体吸收。这项研究的目的是提出一种能够评估消化过程中具有不同结构的脂蛋白基质行为的体外方法。设计了两种成分完全相同的模型矩阵(10%的油,15%的乳清蛋白,w / w):i)由脂肪细小液滴(1微米)制成的液体乳液(LE),分散在包含天然乳清蛋白,ii)由连续乳清蛋白凝胶包裹大油滴(20微米)制成的固体乳剂(SE)。通过基于INFOGEST指南的体外胃肠道方案,使用pH-stat监测蛋白质和脂质的酶促水解,消化这两种基质。通过在相同条件下进一步消化无脂质基质,评估了蛋白水解和脂解反应的作用。在短时间和长时间消化时间之间,基质之间均存在显着差异。由于连续相的凝胶状态,SE的蛋白水解和脂解的初始速率都比LE慢。在实验结束时,SE对脂解的作用较小(DHlip_SE = 51% DHprot_LE = 52%),因为对消化的敏感性更高变性乳清蛋白。这些结果突出了基质结构对酶可及性的影响,并表明该方法适用于监测复杂食品基质的消化。 (C)2015 Elsevier Ltd.保留所有权利。

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