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抗氧化醇溶蛋白颗粒稳定的 Pickering 高内相乳液(HIPEs)作为口服给药系统的研究及其体外消化命运。

Development of antioxidant gliadin particle stabilized Pickering high internal phase emulsions (HIPEs) as oral delivery systems and the in vitro digestion fate.

机构信息

Research and Development Center of Food Proteins, Guangdong Province Key Laboratory for Green Processing of Natural Products and Product Safety, South China University of Technology, Guangzhou 510640, PR China.

出版信息

Food Funct. 2018 Feb 1;9(2):959-970. doi: 10.1039/c7fo01400g. Epub 2018 Jan 11.

Abstract

In this paper, we demonstrate for the first time the use of gliadin particles to structure algal oil (rich in DHA) and to exert chemical stability against lipid oxidation via the Pickering high internal phase emulsion (HIPE) strategy. The gliadin/chitosan colloid particles (GCCPs) were effectively adsorbed and anchored at the algal oil-water interface. Concomitantly, the particle-coated droplets as building blocks constructed a percolating 3D-network framework, endowing Pickering HIPEs with viscoelastic and self-supporting attributes. In addition, Pickering HIPEs loaded with shell (HIP-curEs) or core curcumin (HIPEs-cur) were constructed to depress the oxidation of algal oil. The content of primary (lipid hydroperoxides) and secondary (malondialdehyde and hexanal) oxidation products in HIPEs was lower than that in bulk oil. The oxidative stability of HIPEs was further improved in shell and core curcumin. An in vitro gastrointestinal (GI) model was constructed to characterize the lipid digestion, lipid oxidation as well as curcumin bioaccessibility of the ingested Pickering HIPEs. Lipid oxidation in the Pickering HIPEs was retarded under GI fluids, especially in the presence of core curcumin. The free fatty acid (FFA) fraction released was below 30% for all HIPEs, reflecting that the Pickering HIPEs formed restrict the digestion of fat or oil and potentially help to fight obesity. Interestingly, this route enhanced the bioaccessibility of curcumin from only 2.13% (bulk algal oil) to 53.61% (core curcumin); in particular, it reached 76.82% for shell curcumin. These results help to fill the gap between the physicochemical performance of the gliadin particle stabilized Pickering HIPEs and their potential applications as oral delivery systems of nutraceuticals. This work opens concomitantly an attractive strategy to convert liquid oils into antioxidant soft solids without artificial trans fats, as a potential alternative for PHOs.

摘要

本文首次展示了利用麦醇溶蛋白颗粒构建藻油(富含 DHA)的结构并通过 Pickering 高内相乳液(HIPE)策略赋予其化学稳定性以抵抗脂质氧化。麦醇溶蛋白/壳聚糖胶体颗粒(GCCPs)有效地被吸附并锚定在藻油水界面上。同时,作为构建基块的颗粒包覆液滴构建了一个连续的 3D 网络框架,赋予 Pickering HIPE 粘弹性和自支撑特性。此外,构建了负载壳(HIP-curEs)或核心姜黄素(HIPEs-cur)的 Pickering HIPE 以抑制藻油的氧化。HIPEs 中的初级(脂质氢过氧化物)和次级(丙二醛和己醛)氧化产物的含量低于基础油。壳和核心姜黄素进一步提高了 HIPEs 的氧化稳定性。构建了体外胃肠道(GI)模型来表征摄入的 Pickering HIPE 的脂质消化、脂质氧化以及姜黄素生物利用度。在 GI 流体中,Pickering HIPE 中的脂质氧化得到了延缓,尤其是在存在核心姜黄素的情况下。所有 HIPEs 的游离脂肪酸(FFA)释放分数均低于 30%,表明形成的 Pickering HIPE 限制了脂肪或油的消化,并可能有助于对抗肥胖。有趣的是,这种途径使姜黄素的生物利用度从仅 2.13%(基础藻油)提高到 53.61%(核心姜黄素);特别是对于壳姜黄素,其生物利用度达到了 76.82%。这些结果有助于填补麦醇溶蛋白颗粒稳定的 Pickering HIPE 的物理化学性能与其作为营养保健品口服递送系统的潜在应用之间的差距。这项工作同时开辟了一种有吸引力的策略,即将液体油转化为抗氧化软固体,而无需人工反式脂肪,作为 PHO 的潜在替代品。

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