外水相中天然大分子对W/O/W型多重乳状液性质的影响

通过添加天然大分子提高W/O/W型多重乳状液的稳定性。外水相中添加的乳清分离蛋白(WPI)与羧甲基纤维素(CMC)两种物质形成的混合物,可作为亲水性稳定剂来提高乳状液的稳定性。采用两步法制备W/O/W型多重乳状液,研究不同的外水相pH值、WPI与CMC的比例和添加量对W/O/W型多重乳状液性质的影响;以粒径、zeta-电位、黏度、稳定性等指标确定W/O/W型多重乳状液的最优制备条件。研究结果表明:当pH=6时,WPI与CMC的比例10∶1,添加量4.4%,WPI与CMC相互作用形成的混合物吸附在油水界面,形成的界面膜的厚度及韧性较好,W/O/W型多重乳状液的粒径较小,稳定性较高(79%)。     

酪蛋白酸钠-明胶制备S/O/W乳状液的稳定性

碳酸钙是一种常用的强化钙,然而,其悬浮稳定性差,易产生沉淀,严重限制了碳酸钙在食品加工中的应用.以固/油/水(S/O/W)乳状液形式负载碳酸钙,构建具有特定结构分布的钙-脂质微球,有望改善其溶解性和稳定性.本文以食品级碳酸钙为S相,大豆油为O相,酪蛋白酸钠-明胶为W相,构建S/O/W钙-脂质微球,研究不同质量分数明胶和...     

亲水胶体对含酒精O/W(水包油)乳状液稳定性的影响

研究了卡拉胶、刺槐豆胶,及其混和胶作为稳定剂,对以酪蛋白酸钠稳定的含酒精O/W乳状液体系稳定性的影响.结果表明,单独添加一定浓度的卡拉胶可改善体系的分层稳定性,而单独加入刺槐豆胶会加速体系失稳,当m(卡拉胶)∶m(刺槐豆胶)=4∶1加入到体积分数为15%的酒精乳状液中,加入量为0.02%时体系稳定性最好.同时研究了两多糖的加入方式、热处理时间,以及蔗糖存在下对乳状液稳定性及黏度的影响.结果表明,卡拉胶与刺槐豆胶分别加入到乳状液中稳定效果较好,并且卡拉胶和刺槐豆胶分别在90℃保温6min后加入有利于体系的稳定;质量分数为10%的蔗糖存在增强了复合胶存在下体系的稳定性.     

酒精对酪蛋白酸钠溶液及O/W乳状液的影响

介绍了酒精对酪蛋白酸钠溶液及酪蛋白稳定的O/W乳状液性质的影响 .试验表明酒精在一定程度上可以降低酪蛋白酸钠的溶解度 .界面张力的测定则表明酒精的存在在很大程度上可以降低油—水界面和油—酪蛋白溶液界面的界面张力 .含酒精的乳状液体系的粘度会由于酒精的存在而提高 ,在酒精体积分数达 3 0 %时 ,乳状液体系的粘度会突然大幅度升高 .通过O/W乳状液的分层稳定性测定可发现 ,低浓度的酒精可以提高酪蛋白稳定的乳状液的分层稳定性 ,但酒精质体积分数超过 3 2 %时 ,乳状液的分层稳定性会受到破坏 .含酒精的O/W乳状液体系中油相含量的提高在一定范围内可以提高乳状液的稳定性 ,但高分散相浓度的含酒精的乳状液体系中由于连续相中酒精浓度的提高使乳状液体系稳定性下降 .     

乳化剂、油浓度及油滴粒径对乳状液中油脂氧化稳定性的影响

以过氧化值(POV)为指标,研究了乳化剂类型、油浓度及油滴粒径对O/W乳状液中油脂氧化稳定性的影响.以用十二烷基硫酸钠(SDS)和Tween-80为乳化剂制备的含红花籽油的乳状液为研究对象,结果表明,乳化剂类型和油浓度对乳状液体系中油脂氧化有较显著的影响.用阴离子型表面活性剂SDS稳定的乳状液中的油脂氧化速率明显大于用非离子型Tween-80稳定的乳状液;随着油浓度下降,油脂氧化速率增大.油滴粒径和油脂氧化速率没有显著的相关性.     

鹰嘴豆蛋白肽对水包油型乳状液稳定性的影响

利用碱性蛋白酶对鹰嘴豆蛋白水解1.5 h,研究不同质量浓度(0、5、10、15、20 mg/m L)的鹰嘴豆蛋白肽对乳状液稳定性的影响。测定了乳状液的浊度、乳化稳定性、ζ-电势、分层稳定性、共轭二烯的含量以及鹰嘴豆蛋白肽在乳状液中的分布情况。结果表明:鹰嘴豆蛋白肽能够显著提高O/W型乳状液的稳定性。添加鹰嘴豆蛋白肽后的乳状液浊度、乳化稳定性、ζ-电势值明显增大,并且能够提高乳状液的分层稳定性、降低共轭二烯的生成量。此外,鹰嘴豆蛋白肽能够吸附在油水界面上提高乳状液稳定性。相对于其他质量浓度,鹰嘴豆蛋白肽质量浓度为10 mg/m L时,乳状液的稳定性最好。     

W/O/W多重乳状液的实验研究

研究了W/O/W多重乳状液的制备方法及影响其稳定性的因素。通过正交试验选出较佳的工艺参数,获得了较稳定的W/O/W多重乳状液。     

大豆可溶性多糖与Fe2+对O/W乳状液物理稳定性及流变特性的影响

研究大豆可溶性多糖(soybean soluble polysaccharides,SSPS)及不同浓度的Fe2+对大豆分离蛋白(soy isolated protein,SPI)稳定的O/W乳状液的物理稳定性和流变特性的影响。通过测定14 d内添加SSPS和不同浓度的Fe2+的乳状液的稳定动力学指数(turbiscan stability index,TSI)、稳态流变、粒径大小及分布和Zeta-电位,确定其物理稳定性。结果表明,与SPI乳状液相比,添加SSPS后,SSPS-SPI乳状液的TSI显著降低(p<0.05),液滴的表面积平均直径(d_3,2)和体积平均直径(d_4,3)增加,粘度系数增加,Zeta-电位绝对值降低,表明SSPS增加了SPI乳状液的粘度,提高了乳状液的物理稳定性;添加0.1 mmol/L Fe2+后,乳状液的TSI最低,液滴的d_3,2和d_4,3分别为0.686、2.136 μm,为最小粒径,粘度增加,稳定性较好;随着Fe2+浓度的增加,乳状液的TSI显著增加(p<0.05),粒径增大,分布范围变宽,表明0.2~0.5 mmol/L的Fe2+降低了乳状液的物理稳定性。总之,SSPS和0.1 mmol/L Fe2+的添加,提高了SPI稳定的O/W乳状液的物理稳定性。     

电导率法研究O/W型罗非鱼油乳状体系的稳定性

以一定浓度的Tween80、Tween20、Span20、SDS、酪朊酸钠、大豆卵磷脂为乳化剂,制备了不同的罗非鱼油乳状液,探讨了在不同油水比例、不同pH的条件下,O/W型中富水相(下相)的电导率变化规律.结果表明,以0.15%Tween80与0.55%大豆卵磷脂复配的乳化剂.在油水比为35:65的O/W型罗非鱼油乳状体系中,pH4乳状液的稳定性低于pH7与pH9.用电导率法来研究O/W型罗非鱼油乳状体系的稳定性,具有快速、简洁的优点.     

猪血浆蛋白水解物对水包油型乳状液氧化稳定性的影响

本实验主要研究了猪血浆蛋白水解物(Porcine plasma protein hydrolysate,PPPH)对水包油型(O/W型)乳状液储藏过程氧化稳定性的影响。分别将PPPH以0、2.5、5、10和20 mg/m L的浓度添加到以Tween-20为乳化剂的菜籽油O/W型乳状液中,测定乳状液在37℃条件下储藏10 d时间内的荧光光谱分析、共轭二烯(Conjugated diene,CD)和硫代巴比妥酸值(Thiobarbituric acid reactive substances,TBARS)的变化趋势。研究结果表明,色氨酸的氧化降解发生在蛋白氧化的初级阶段,而荧光蛋白氧化产物(Fluorescent protein oxidation products,FP)的形成是蛋白氧化第二阶段的产物。另外,在乳化体系储藏期间,与对照组相比,添加2.5 mg/m L PPPH的处理组具有最高的色氨酸荧光强度和FP(p0.05),同时具有最低的CD和TBARS值(p0.05)。与此同时,色氨酸荧光强度与CD含量和TBARS值之间呈现显著的负相关关系。总之,PPPH的添加能够显著提高O/W型乳状液的氧化稳定性,为其作为抗氧化剂在乳状液食品中的潜在应用奠定了理论基础。     

Surface-active solid lipid nanoparticles as Pickering stabilizers for oil-in-water emulsions

Oil-in-water (O/W) emulsions solely stabilized by surface-active solid lipid nanoparticles (SLNs) were developed. The SLNs were generated by quench-cooling hot O/W nanoemulsions consisting of 7.5% glyceryl stearyl citrate (GSC) dispersed in water. Their initial volume-weighted mean particle diameter (～152 nm) and zeta potential (ca.-49 mV) remained unchanged for 24 weeks. O/W emulsions (oil phase volume fraction: 0.2) containing 7.5% (w/w) GSC SLNs in the aqueous phase were kinetically-stable for 12 weeks and did not visually phase-separate over 24 weeks. The O/W emulsions generated with solid-state GSC SLNs had a volume-weighted mean oil droplet diameter of ～459 nm and a zeta potential of ca.-43 mV. Emulsion microstructure evaluated with TEM revealed dispersed oil droplets sparsely covered with adsorbed Pickering-type SLNs as well aggregated SLNs present in the continuous phase. Gradual emulsion destabilization resulted from GSC SLN dissolution during the experimental timeframe. Overall, surface-active SLNs developed via nanoemulsions effectively kinetically stabilized O/W emulsions.     

Effects of water-soluble soybean polysaccharide on rheological properties,stability and lipid digestibility of oil-in-water emulsion during in vitro gastrointestinal digestion

Water-soluble soybean polysaccharide (SSPS) is a naturally occurring emulsifier. SSPS was used as the sole emulsifier to stabilize an oil-in-water (O/W) emulsion. The effects were investigated of different SSPS concentrations (3–20% (w/w)) on the lipid digestibility, rheological properties and stability of O/W emulsions during in vitro digestion model. The droplet size of the emulsions tended to increase during the oral phase because the emulsions were unstable and droplets coalesced, except with a SSPS concentration of 20% (w/w). The presence of SSPS markedly reduced the free fatty acid (FFA) content after its stabilized O/W emulsion passed through in vitro gastrointestinal digestion. The amount of FFA significantly decreased as the concentration of SSPS increased due to SSPS stabilization film on oil droplet surface and high viscous system. SSPS may be an attractive alternative ingredient to control the lipid digestibility of emulsions for various food products.     

Release rate profiles of magnesium from multiple W/O/W emulsions

Water-in-oil-in-water (W/O/W) emulsions were formulated based on rapeseed oil, olive oil, olein and miglyol. Polyglycerol polyricinoleate and sodium caseinate were used as lipophilic and hydrophilic emulsifiers, respectively. Magnesium was encapsulated in the inner aqueous droplets. Emulsion stability was assayed through particle sizing and magnesium release at two storage temperatures (4 and 25 °C) over 1 month. Irrespective of the oil nature, both the primary W/O and W/O/W emulsions were quite stable regarding the size parameters, with 10-μm fat globules and 1-μm internal water droplets. Magnesium leakage from W/O/W emulsions was influenced by the oil type used in the formulation: the higher leakage values were obtained for the oils characterized by the lower viscosity and the higher proportion of saturated fatty acids. Magnesium release was not due to droplet–globule coalescence but rather to diffusion and/or permeation mechanisms with a characteristic rate that varied over time. In addition, W/O/W emulsions were resistant to various thermal treatments that mimicked that used in pasteurization processes. Finally, when W/O/W emulsions were placed in the presence of pancreatic lipase, the emulsion triglycerides were hydrolysed by the enzyme. These results indicated a possible use of W/O/W emulsions loaded with magnesium ions in food applications.     

一种水包油包胶型乳液的制备及其在乳化肠中的应用

以结冷胶和无水氯化钙为内水相凝固剂,酪蛋白酸钠为外水相乳化剂,制备一种水包油包胶（S/O/W）型 乳液。以多重乳液粒径和分布为指标,研究酪蛋白酸钠添加量对S/O/W型多重乳液加工适应性的影响。结果表明： 正交试验得到S/O型单重乳液最佳制备条件为：内水相中结冷胶添加量0.2%、无水氯化钙添加量0.5%;内水相乳化 剂聚甘油蓖麻醇酯添加量2.5%;油相为精炼猪油,油水体积比3∶2;剪切速率17 500 r/min,剪切时间1.5 min。将制 得的S/O型单重乳液与不同添加量酪蛋白酸钠混合制得S/O/W型多重乳液。当酪蛋白酸钠添加量0.1%时,S/O/W型 多重乳液粒径符合加工要求,且贮藏、热处理、剪切稳定性较好。以多重乳液替代猪脂肪制备的低脂乳化肠与高脂 （精炼猪油含量20%）乳化肠外观不存在明显差异;微观结构观察结果表明,多重乳液在乳化肠中包裹良好、分布 均匀。     

Microbial cells as colloidal particles: Pickering oil-in-water emulsions stabilized by bacteria and yeast

Thermally-inactivated baker's yeast (Saccharomyces cerevisiae) and lactic acid bacteria (Lactobacillus acidophilus and Streptococcus thermophilus) were used to generate and stabilize model oil-in-water (O/W) emulsions containing up to 80 wt.% dispersed oil. With optimized compositions, cell-covered dispersed oil droplets were stable against droplet coalescence and bulk phase separation for over four months. From a textural perspective, these emulsions were self-supporting and exhibited a mayonnaise-like consistency. The microbial cells acted as Pickering-type stabilizers by residing at the oil–water interface. The three-phase contact angle of the yeast at the oil–water interface measured using confocal microscopy was 30 ± 9°, demonstrating its ability to stabilize O/W emulsions. These microbial cells may be used in the design of processed food emulsions with an ‘all-natural’ designation as well as for the replacement of common synthetic surfactants to permit clean label declarations.     

Effects of enzymatically modified starch on the encapsulation efficiency and stability of water-in-oil-in-water emulsions

The present study was performed to investigate the possibility of using 4-α-glucanotransferase (4αGTase)-treated starch in W/O/W emulsions to increase their encapsulation efficiency (EE) and stability. Emulsions were prepared using soybean oil, polyglycerol polyricinoleate (PGPR), 4αGTase-treated starch and Tween 20. The mean diameter of W/O/W droplets ranged from 4 to 10 μm depending on the sonication time. When the dye was loaded in the internal water phase, the emulsion prepared by sonication for 1 and 2 min showed a high EE of the dye (>90%). The W/O/W emulsion prepared by sonication for 3 min showed an EE of <90%, but this EE was improved by adding 4αGTase-treated starch to the internal water phase. 4αGTase-treated starch was added to the internal water phase of W/O/W emulsions prepared with a low concentration of PGPR, and the PGPR concentration required to maintain an EE >90% was reduced. W/O/W emulsions containing 4αGTase-treated starch also showed better stability against heating and shearing stresses. These results indicated that 4αGTase-treated starch could be used in the preparation of W/O/W emulsions, which would allow the formulation of W/O/W emulsions with a reduced surfactant concentration.     

Study of commodity properties of food emulsions Part 1. The effect of dispersion medium composition on kinetic stability of O/W emulsions containing proteins,acidic polysaccharides and calcium salts

The effect of concentrations of acidic polysaccharide and calcium ions on the kinetic stability, viscosity and dispersity of protein-containing O/W emulsions is studied. Variation of kinetic stability of the emulsions studied is independent of dispersion composition. In a wide range of calcium acetate concentrations a correlation is observed between kinetic stability and viscosity of emulsions at sodium alginate concentration in the dispersion medium ≤ 0.3%. The transition zone between liquid solution and gel is widened in the presence of sodium caseinate. Maximum kinetic stability is reached at calcium acetate: sodium alginate concentrations of 1.0-1.2 and ～ 6.0, corresponding to optimum conditions for formation of homogeneous crosslinked structures of calcium alginate and calcium caseinate.     

Whey protein-stabilized emulsion properties in relation to thermal modification of the continuous phase

The aim of the present study was to investigate the effect of the protein heat treatment on the physical properties of whey protein concentrate dispersions and the resulting protein-stabilized 30% O/W emulsions. Protein preheating influenced protein particles sizes, viscosity, density, emulsifying capacity and conductivity of protein dispersions. Emulsion stability was improved by protein heat treatment. The emulsions showed bimodal particle size distributions and higher particle sizes with increasing temperature. Thermal modification of the continuous phase influenced flow characteristics of the emulsions and did not affect emulsion conductivity. Heating of whey proteins may generate stable nano-particles and/or aggregates that are able to improve stability of the emulsions. These small structures may stabilize the emulsions by increasing viscosity of the continuous phase and by taking part in formation of the second protein layer on the oil droplets.     

Effects of lipophilic and hydrophilic antioxidants in oil-in-water emulsions under chlorophyll photosensitization

Antioxidative or prooxidative properties of α-tocopherol, Trolox, ascorbic acid, and ascorbyl-palmitate at the concentration of 0.1 and 1.0 mM were determined in oil-in-water (O/W) emulsions under chlorophyll photosensitization. Headspace oxygen depletion, lipid hydroperoxides, and headspace volatile analyses were conducted to determine the oxidative stability of O/W emulsions. For 32 h visible light irradiation, depleted headspace oxygen content in O/W emulsions were in the order of samples containing Trolox, ascorbic acid, ascorbyl palmitate, α-tocopherol, without antioxidants under light, and samples in the dark, which implies that all the added compounds acted prooxidant. These prooxidative properties of added compounds can be observed in the results of lipid hydroperoxides and headspace volatiles. Samples containing ascorbic acid and ascorbyl palmitate retained higher chlorophyll content than those containing Trolox up to 16 h. Increases of concentration of Trolox, ascorbic acid, and ascorbyl palmitate from 0.1 to 1.0 mM increased the lipid oxidation products whereas α-tocopherol decreased the degree of lipid oxidation implying α-tocopherol may not share the same prooxidant mechanisms compared to other compounds in chlorophyll sensitized O/W emulsions.     

“Influence of physicochemical properties of enzymatically modified starch gel on the encapsulation efficiency of W/O/W emulsion containing NaCl”

We investigated the molecular characteristics of 4-α-glucanotransferase (4αGTase)-modified rice starch (MRS) and corn starch (MCS) gels and the NaCl release properties depending on their mechanical properties. Also, encapsulation efficiency (EE) and oil globule size of water-in-oil-in-water (W/O/W) emulsions containing MRS or MCS in the inner aqueous phase (W₁) with NaCl as a model core material were measured after preparation and 14 days of storage. The characteristics of MRS and MCS were examined by analyzing amylose content, molecular fine structure, microstructure, and mechanical properties to better understand their associations with emulsion stability. At 20 % concentration, the gel strength of MCS (~10⁵ pa) was greater than that of MRS (~10³ pa) as MCS had higher apparent amylose content than MRS. The rate of NaCl release from the gel was highly correlated with the gel strength that depended on the type and concentration of the enzymatically-modified starch. As the gel strength increased, EE of freshly prepared and stored W/O/W emulsions increased. Osmotic swelling of NaCl-containing W/O/W was significantly reduced with the incorporation of the modified starch gels in W₁ phase. These results indicated that physicochemical properties of 4αGTase-modified starch gels in W/O/W emulsions largely affected the encapsulation efficiency and stability of the emulsions, which could be utilized to formulate W/O/W emulsions with improved stability and the potential for broader applications.