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海藻酸钠基水包油乳液在体外生理预吸收消化条件下的胃内结构化能力研究

Study of intragastric structuring ability of sodium alginate based o/w emulsions under in vitro physiological pre-absorptive digestion conditions.

作者信息

Soukoulis Christos, Fisk Ian D, Bohn Torsten, Hoffmann Lucien

机构信息

Environmental Research and Innovation (ERIN) Department, Luxembourg Institute of Science and Technology (LIST), 41, rue du Brill, L-4422 Belvaux, Luxembourg.

Division of Food Sciences, School of Biosciences, University of Nottingham, Sutton Bonington, LE12 5RD Leicestershire, United Kingdom.

出版信息

Carbohydr Polym. 2016 Apr 20;140:26-34. doi: 10.1016/j.carbpol.2015.12.021. Epub 2015 Dec 12.

Abstract

In the present work, the intragastric structuring ability of o/w emulsions either stabilised (1-4%, w/w of sodium alginate (SA)) or structured with sheared ionic gel (1-3%, w/w of SA crosslinked with Ca(2+)) in the absence (saliva and gastric phases constituted of deionised water) or presence of in vitro pre-absorptive conditions (physiological simulated saliva and gastric fluids) was investigated. Visualisation of the morphological aspects of the gastric chymes, in the absence of multivalent counterions, demonstrated that SA stabilised systems underwent a remarkable swelling in the pH range of 2-3, whilst at the same pH range, ionic SA gel structured systems maintained their major structure configuration. When the aforementioned systems were exposed to physiological intragastric fluids, a reduction of the length and the hydrodynamic volume of the alginate fibres was detected regardless the structuring approach. On their exposure to physiological intragastric conditions (pH=2), SA stabilised emulsions underwent sol-gel transition achieving a ca. 3- to 4-order increase of storage modulus (at 1Hz). In the case of ionic sheared gel structured emulsions, exposure to physiological intragastric fluids resulted in a 10-fold reduction ability of their acid structuring ability, most likely due to the dialysis of egg-box dimer conformations by monovalent cations and protons and the sterical hindering of hydrogen bonding of MM and GG sequences under acidic conditions. Using of non-physiological simulated intragastric fluids was associated with overestimated structuring performance of SA regardless its physical state.

摘要

在本研究中,研究了在不存在(由去离子水构成的唾液和胃相)或存在体外预吸收条件(生理模拟唾液和胃液)的情况下,经稳定化处理(海藻酸钠(SA)含量为1 - 4%,w/w)或用剪切离子凝胶构建(SA与Ca(2+)交联,含量为1 - 3%,w/w)的水包油乳液的胃内构建能力。在不存在多价抗衡离子的情况下,对胃糜形态方面的观察表明,SA稳定化体系在pH值为2 - 3的范围内会发生显著膨胀,而在相同pH范围内,离子型SA凝胶构建体系保持其主要结构构型。当上述体系暴露于生理胃液中时,无论构建方法如何,均可检测到藻酸盐纤维长度和流体动力学体积的减小。在暴露于生理胃内条件(pH = 2)时,SA稳定化乳液发生溶胶 - 凝胶转变,储能模量(在1Hz时)增加约3至4个数量级。对于离子型剪切凝胶构建的乳液,暴露于生理胃液会导致其酸构建能力降低10倍,这很可能是由于单价阳离子和质子对蛋盒二聚体构象的透析作用以及在酸性条件下MM和GG序列氢键的空间位阻作用。使用非生理模拟胃液会导致无论SA处于何种物理状态,其构建性能都被高估。

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