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用于在乳制品中口服递送黄连素的可食用油凝胶:体外消化研究。

Edible oleogels for oral delivery of berberine in dairy food: In-vitro digestion study.

作者信息

Sarraf Mozhdeh, Beigbabaei Adel, Naji-Tabasi Sara

机构信息

Department of Food Chemistry Research Institute of Food Science and Technology (RIFST) Mashhad Iran.

Department of Food Nanotechnology Research Institute of Food Science and Technology (RIFST) Mashhad Iran.

出版信息

Food Sci Nutr. 2024 Apr 5;12(5):3273-3281. doi: 10.1002/fsn3.3994. eCollection 2024 May.

Abstract

Oleogel is a viscoelastic, spreadable and semi-solid structure, which is used as a fat substitute and a controller the release of bioactive compounds. The aim of this study was to develop low fat dairy dessert enriched with berberine with applying oleogel system as delivery system and fat replacer. The oleogel prepared with an emulsion-templated methods based on soluble interaction of whey protein concentrate (WPC), WPC-basil seed gum (BSG), and WPC-xanthan gum (XG). In the first step, berberine release kinetic in in-vitro gastrointestinal environment was studied. The results showed that the mouth environment had the highest release rate of berberine. Cooperation of hydrocolloids in oleogel increase stability of structure in stomach condition in compared with WPC oleogel. The suitable model to fit the oleogels contain beberine was the Korsmeyer-Papas that was the highest (.98). According to release results of berberine from oleogel network, the oleogel 0.6BSG:WPC was chosen and applied in formulation of dairy dessert at different levels (0%, 25%, 50%, 75% and 100% of oleogel) instead of cream. The dessert contained uncoated berberine had the unacceptable bitterness in comparison with samples containing coated berberine with oleogel. The overall acceptance decreased with increment of oleogel due to increasing of bitter taste. Appling berberine (therapeutic compound) and oleogel (fat-substitute) to achieve marketable consumer products showed positive effects on trend of the study, especially at low level of substitution.

摘要

油凝胶是一种具有粘弹性、可涂抹的半固体结构,用作脂肪替代品和生物活性化合物释放的控制剂。本研究的目的是开发富含黄连素的低脂乳制甜点,应用油凝胶体系作为递送系统和脂肪替代品。该油凝胶采用基于乳清浓缩蛋白(WPC)、WPC-罗勒籽胶(BSG)和WPC-黄原胶(XG)的可溶性相互作用的乳液模板法制备。第一步,研究了黄连素在体外胃肠道环境中的释放动力学。结果表明,口腔环境中黄连素的释放速率最高。与WPC油凝胶相比,油凝胶中亲水胶体的协同作用提高了胃环境中结构的稳定性。拟合含黄连素油凝胶的合适模型是Korsmeyer-Papas模型,其拟合度最高(R²=0.98)。根据黄连素从油凝胶网络中的释放结果,选择0.6BSG:WPC油凝胶并以不同水平(油凝胶的0%、25%、50%、75%和100%)应用于乳制甜点配方中以替代奶油。与含油凝胶包衣黄连素的样品相比,含未包衣黄连素的甜点有不可接受的苦味。由于苦味增加,总体接受度随着油凝胶用量的增加而降低。应用黄连素(治疗性化合物)和油凝胶(脂肪替代品)来获得适销对路的消费产品对本研究趋势显示出积极影响,尤其是在低替代水平时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb01/11077212/c7b423c30b01/FSN3-12-3273-g003.jpg

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