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蔗糖酯的亲水亲油平衡值对双凝胶体系理化性质的影响

The Effect of the HLB Value of Sucrose Ester on Physiochemical Properties of Bigel Systems.

作者信息

Golodnizky Daniel, Davidovich-Pinhas Maya

机构信息

Faculty of Biotechnology and Food Engineering, Technion-Israel Institute of Technology, Haifa 3200003, Israel.

Russell-Berrie Nanotechnology Institute, Technion-Israel Institute of Technology, Haifa 3200003, Israel.

出版信息

Foods. 2020 Dec 12;9(12):1857. doi: 10.3390/foods9121857.

Abstract

The current research explored the effect of different sucrose esters (SEs), with different hydrophilic-lipophilic balance (HLB) values, on bigel structure and properties. Bigels consisting of a water phase with glycerol and gelatin and an oil phase with glycerol mono-stearate, lecithin, and SEs with different HLB values were prepared. Rheological and thermal analyses revealed similar gelation-melting transitions governed by glycerol-monostearate crystallization (at ≈55 °C) for all bigel samples. The bigel matrix of the H1 and H2 samples (bigels consisting of SEs with HLBs of 1 and 2, respectively) demonstrated physical gel rheological characteristics of higher elastic and solid-like behavior compared with the H6 sample (bigel consisting SE with HLB 6). A similar trend was observed in the mechanical analysis with respect to hardness, firmness, and spreadability values, which were in the order of H1 > H2 > H6. This behavior was attributed to droplet size observed in the microscopy analysis, revealing significantly smaller droplets in the H1 and H2 samples compared with the H6 sample. These differences in droplet size were attributed to the diffusion kinetics of the low-molecular-weight surfactants. More specifically, the ability of mono-esterified SEs to diffuse faster than fully esterified SEs due to lower molar mass leads to a higher SE content at the oil-in-water (O/W) interface as opposed to the bulk oil phase. The results demonstrate the importance of the interface content in O/W bigel systems, providing an effective way to alter and control the bigel bulk properties.

摘要

当前研究探讨了具有不同亲水亲油平衡(HLB)值的不同蔗糖酯(SEs)对双凝胶结构和性质的影响。制备了由含有甘油和明胶的水相以及含有单硬脂酸甘油酯、卵磷脂和不同HLB值的SEs的油相组成的双凝胶。流变学和热分析表明,所有双凝胶样品的凝胶化-熔融转变相似,均由单硬脂酸甘油酯结晶(约55°C)控制。与H6样品(由HLB为6的SE组成的双凝胶)相比,H1和H2样品(分别由HLB为1和2的SE组成的双凝胶)的双凝胶基质表现出更高弹性和类固体行为的物理凝胶流变学特性。在硬度、紧实度和铺展性值的力学分析中也观察到类似趋势,顺序为H1>H2>H6。这种行为归因于显微镜分析中观察到的液滴尺寸,与H6样品相比,H1和H2样品中的液滴明显更小。液滴尺寸的这些差异归因于低分子量表面活性剂的扩散动力学。更具体地说,由于摩尔质量较低,单酯化SEs比完全酯化SEs扩散得更快,导致油水(O/W)界面处的SE含量高于本体油相。结果证明了O/W双凝胶体系中界面含量的重要性,为改变和控制双凝胶整体性质提供了一种有效方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc2e/7763610/2a255f3a48ea/foods-09-01857-g001.jpg

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