Fish Oil Microcapsules from O/W Emulsions Produced by Premix Membrane Emulsification

Fish oil microcapsules were prepared by combining a low-energy emulsification method (premix membrane emulsification) with spray drying. Oil-in-water (O/W) emulsions were prepared using a two-step emulsification method that used a rotor–stator homogenizer followed by membrane emulsification. The influence of the emulsification method (mechanical stirring or membrane emulsification), the emulsification conditions (membrane and emulsifier type), and the amount of wall material on the physicochemical characteristics of the microcapsules was studied. The results show that the emulsification method and the type and amount of emulsifier and wall material affect the final amount of encapsulated oil. Microcapsules produced by membrane emulsification and stabilized with 2 % Tween-20 or 10 % whey protein presented the highest values (higher than 50 %) of oil encapsulation efficiency (OEE). It has been found that the OEE increases when decreasing the droplet size of the emulsions as well as with the increase of the amount of wall material employed during drying. Morphology analysis showed that the microcapsules obtained from O/W emulsions produced by premix membrane emulsification were rounder in shape, without visible cracks on the surface and no vacuoles on the inside. Oxidation stability tests performed on some selected samples indicate that the microcapsules with higher stability are the ones produced with a higher amount of wall material and have less surface oil.     

Production of O/W Emulsions Containing Astaxanthin by Repeated Premix Membrane Emulsification

ABSTRACT: Oil-in-Water (O/W) emulsions are mainly produced by application of high mechanical stress or by membrane emulsification processes at low pressures. Advantages such as narrower droplet size distribution and lower operating costs make membrane emulsification processes more suitable for producing astaxanthin-loaded O/W emulsions. The characteristics of 1 of these membrane emulsification methods, called repeated premix membrane emulsification, are studied in this work. In this emulsification process, a pre-emulsion is repeatedly pushed through a hydrophilic or hydrophobic membrane. In this research, ahydrophilic membrane was used because the objective was to obtain an O/W emulsion. Pre-emulsions were produced by dispersing palm oil containing dissolved astaxanthin in water. The oil droplets were stabilized with a combination of 2 emulsifiers. Each O /W emulsion passed the membrane 3 times underpressures and disperse phase fractions of 5 to 15 bar and from 10 wt% to 40 wt%, respectively. To investigate the production of O/W emulsions by repeated premix membrane emulsification, mean Sauter diameters and fluxes were measured. To find the optimal ranges of pressure and dispersed phase fraction, a "2-level factorial design with central composite and stars points" experimental design was applied.     

Preparation of Monodisperse Food-Grade Oleuropein-Loaded W/O/W Emulsions Using Microchannel Emulsification and Evaluation of Their Storage Stability

W/O/W emulsion is an emerging system in developing new functional and low-calorie food products. The aim of this study is to produce food-grade monodisperse water-in-oil-in-water (W/O/W) emulsions loaded with a hydrophilic bioactive oleuropein. W/O/W emulsions were prepared via high-pressure homogenization and subsequent microchannel (MC) emulsification. The internal aqueous phase was a 5-mM sodium phosphate buffer containing d(+)-glucose (5 wt.%) and oleuropein (0.1–0.7 wt.%). The oil phase consisted of soybean oil and tetraglycerin monolaurate condensed ricinoleic acid esters (TGCR; 3–8 wt.%). The external aqueous phase was a 5-mM sodium phosphate buffer containing d(+)-glucose (5 wt.%) and decaglycerol monolaurate (1 wt.%). Oleuropein-loaded submicron W/O emulsions with average droplet diameters as small as 0.15 μm and monomodal droplet size distributions were prepared by high-pressure homogenization when applying high TGCR concentrations of 5–8 wt.% and low oleuropein concentrations of 0.1–0.3 wt.%. Monodisperse oleuropein-loaded W/O/W emulsions with average W/O droplet diameters of around 27 μm and coefficients of variation of below 5 % were successfully prepared when using a silicon MC array plate with wide channels of 5-μm depth and 18-μm width. The monodisperse W/O/W emulsions prepared at high TGCR concentrations and low oleuropein concentrations were the most stable during 40 days of storage. The adsorption behavior of oleuropein at the internal aqueous–oil interface was relevant to W/O/W emulsions microstructure and stability. The results are believed to provide useful information for successfully preparing stable monodisperse W/O/W emulsions loaded with hydrophilic functional compounds. The surface activity of the loaded material seems to be a key parameter in optimizing the formulation of W/O/W food emulsion.     

Water/Oil Emulsions Prepared by the Membrane Emulsification Method and Their Stability

We developed and tested a simple method to measure dispersed droplet size of W/O emulsions. Then, using a microporous glass membrane treated with oil phase, we produced a W/O emulsion with high water content (40% w/w) at a high emulsification rate by the membrane emulsification method, and assessed its stability. In comparison with emulsions by the stirring methods, variations in dispersed droplet size and viscosity of emulsions by membrane method were small and the emulsions were more stable. Droplet size was not related to the stability of the W/O emulsion prepared by membrane emulsification.     

Viscosity change in oil/water food emulsions prepared using a membrane emulsification system

This paper reports viscosity measurements of oil/water (O/W) monodispersed emulsions of different droplet diameters obtained in a membrane emulsification system. Hydrophilic microporous glass membranes of different pore diameters were used to prepare O/W emulsions. The results showed that the droplet diameter of the emulsions varied with the average pore diameter of the membrane. The average droplet diameter was found to be about five times greater than the average membrane pore diameter. A correlation was found for the relationship between the average droplet diameter and the emulsion viscosity. As the dispersed droplet size became smaller, the total surface area of the droplets increased. Therefore, the emulsion viscosity and the relative viscosity increased. Few studies have reported the viscosity of O/W emulsions with droplet diameter of 5 μm or more and an oil phase concentration of 10 vol% or less. In the present study a correlation between the droplet diameter and the emulsion viscosity was statistically established. ©     

Behaviour of oil droplets during spray drying of milk-protein-stabilised oil-in-water emulsions

The effects of spray drying on the behaviour of oil droplets in oil-in-water emulsions (12.0%, w/w, maltodextrin; 20.0%, w/w, soya oil) stabilised with either sodium caseinate or whey protein isolate (WPI) were examined as a function of protein concentration (0.5–5.0%, w/w). Spray drying and redispersion caused a shift in the droplet size distribution to larger values for all emulsions made using low protein concentrations (0.5–2.0%, w/w), in comparison with their respective parent emulsions. However, the droplet size distribution was affected only very slightly by spray drying when the protein concentration was above 2.0% (w/w). The effects of maltodextrin concentration (1.0–25.0%, w/w) on the behaviour of WPI-stabilised emulsions (0.5–10.0%, w/w, WPI, 20.0%, w/w, soya oil) were also examined. Emulsions containing low levels of maltodextrin showed marked re-coalescence during spray drying and redispersion even at a WPI concentration of 10.0% (w/w).     

不同壁材制备油茶籽油微胶囊的研究

研究以大豆分离蛋白、酪朊酸钠、麦芽糊精、大豆膳食纤维和阿拉伯胶为壁材,通过复配组合,利用喷雾干燥法制备油茶籽油微胶囊产品,同时以乳化稳定性、微胶囊化效率和产率、微胶囊形态的微观表征颗粒完整率和微胶囊感官品质评价为评定指标,比较不同壁材组合得到的微胶囊产品之间的差异。结果表明,以大豆分离蛋白、酪朊酸钠和麦芽糊精为复配壁材的油茶籽油微胶囊产品为乳白色粉末,具有良好冲调性和流动性,微胶囊化效率83.62%和产率63.87%,微胶囊形态的颗粒完整率接近70%,是较好的喷雾干燥制备油茶籽油微胶囊产品的复配壁材之一。     

Effect of chitosan on the stability and properties of modified lecithin stabilized oil-in-water monodisperse emulsion prepared by microchannel emulsification

The effect of chitosan (CHI) on the stability of monodisperse modified lecithin (ML) stabilized soybean oil-in-water (O/W) emulsion was investigated. Monodisperse emulsion droplets with particle size of 24.4 ± 0.7 μm and coefficient of variation below 12% were prepared by microchannel (MC) emulsification using a hydrophilic asymmetric straight-through MC silicon 24 × 24 mm microchip consisting of 23,348 microchannels. The stability of the ML stabilized monodisperse emulsion droplets was investigated as a function of CHI addition at various concentration, pH, ionic strength, thermal treatment and freezing-thawing treatment by means of particle size and ζ-potential measurements as well as microscopic observation. The monodisperse O/W emulsions were diluted with CHI solution at various concentrations to a final droplet concentration of 1 wt% soybean oil, 0.25 wt% ML and 0–0.5 wt% CHI at pH 3. Pronounced droplet aggregation was observed when CHI was present at a concentration range of between 0.01 and 0.04 wt%. Above this concentration range, flocculations were less extensive, indicating some restabilization. ML stabilized emulsions were stable at a wide range of NaCl concentrations (0–1000 mM) and pH (3–8). On the contrary, in the presence of CHI, aggregation of the emulsion droplets was observed when NaCl concentration was above 200 mM and when the pH started to approach the pKa of CHI (i.e. ∼6.2–7.0). Emulsions containing CHI were found to have better stability at high temperature (>70 °C) in comparison to the emulsion stabilized only by ML. With sucrose/sorbitol as cryoprotectant aids, emulsions with the addition of CHI were found to be more resistant to droplet coalescence as compared to those without CHI after freezing at −20 °C for 22 h and thawing at 30 °C for 2 h. The use of CHI may potentially destabilize ML-stabilized O/W emulsions but its stability can be enhanced by selectively choosing the appropriate CHI concentrations and conditions of preparation.     

Influence of homogenisation conditions and drying method on physicochemical properties of dehydrated emulsions containing different solid components

Dehydrated o/w emulsions containing sodium caseinate and lactose (sample 1), and gelatine, sucrose and maltodextrin (DE 10) (sample 2) were used to study the influence of homogenisation conditions – homogenisation pressure (15 and 70 MPa) and number of passes (1 and 2) – and the drying method – spray‐drying vs. freeze‐drying – on physicochemical parameters, including oil microencapsulation efficiency (ME), oil droplet size in reconstituted emulsions, water activity, glass transition temperature, powder bulk density and time for emulsion reconstitution in water. Results showed that small and uniform oil droplets attained with increased homogenisation pressure were not sufficient for high oil encapsulation. The permeability of the solid wall to the extraction solvent appeared to be the dominant factor, and this may increase with homogenisation pressure. With the exception of oil droplet size in sample 1 and ME in sample 2, the drying method exerted larger changes in the physicochemical parameters studied than the homogenisation pressure. For sample 2, significant changes in the ME were not observed between the freeze‐dried and spray‐dried samples, even though a great emulsion destabilisation was observed in the reconstituted emulsion of the latter.     

多重油脂微胶囊乳液喷雾干燥粉工艺及其理化性质

为提高膳食中脂肪酸组成多样性，本研究以多重脂肪酸组成的复合油脂（玉米油、黄油、椰子油、藻油）为芯材，麦芽糊精、乳清蛋白浓缩物、酪蛋白酸钠为主要壁材，通过微射流耦合食品乳化剂制得O/W型均匀乳液，经喷雾干燥制得粉末微胶囊，利用单因素实验结合响应面分析包埋率影响因素，优化了最佳制备工艺: 进风温度170 ℃、均质压力31 MPa、乳化剂添加量0.3%，该产品的油脂包埋率高达85.75%。红外光谱（FTIR）分析证实油脂通过微胶囊得到了较好包埋，扫描电镜（SEM）图像显示产品表面虽略有凹陷但是结构致密完整。实验发现产品粉末的复原乳液液滴平均粒径为241.8 nm，zeta电位为-33.1 mV，显示该产品具有良好的复溶性与稳定性；激光共聚焦扫描显微镜（CLSM）发现油脂完整包埋且可均匀悬浮，显示微胶囊复原乳中油脂的保护效果好。     

Optimization of nano-emulsions production by microfluidization

The purpose of this study was to produce an oil-in-water nano-emulsion with different compositions of the continuous and dispersed phases through microfluidization. The aqueous phase was a solution of maltodextrin with five different emulsifying ingredients including modified starch (Capsul and Hi-Cap), sodium caseinate (SC), whey protein hydrolysate (WPH), or whey protein concentrate (WPC), while the oil phase consisted of d-limonene or fish oil. Results showed that micofluidizer was capable of producing nano-emulsions (D32 as small as 150 nm) with a narrow size distribution. Generally, moderate microfluidization pressures (42–63 MPa) and cycles (1–2) were the optimum conditions beyond which, there were adverse changes in the emulsion size. For the two oils tested as the dispersed phase, fish oil emulsions had lower Sauter mean diameters (D32) but with wider size distributions than d-limonene. When different emulsifying ingredients were compared, Hi-Cap produced nano-emulsions with the narrowest distribution but highest D32 (about 600 nm). Nano-emulsions with WPC had the smallest D32 (about 200 nm) but the widest size distribution. It was found that a d-limonene volume fraction of 0.10 was the optimum dispersed-phase concentration in terms of emulsion droplet size (D32). Also, adding a surfactant (Tween 20) helped to reduce the emulsion size significantly during microfluidization, but it lead to extensive flocculation of emulsion droplets because of surfactant–biopolymer interactions and emulsifier displacement.     

Influence of Ultrasonication Parameters on Physical Characteristics of Olive Oil Model Emulsions Containing Xanthan

Ultrasonic emulsification of 20-wt.% o/w emulsions (pH 3.8) containing a food-grade emulsifier (whey protein isolate, WPI, 2.7 wt.%) and xanthan gum (XG, 0.25 wt.%) was performed. Time and amplitude of ultrasonic treatment changed in order to evaluate their influence on emulsion droplet size, viscosity, and stability (by multiple light scattering (MLS) profiles) during cold storage (10 days at 5 °C). Ultrasonic treatment duration changed from 1 to 4 min at constant amplitude of 70 %. Considering the amplitude, intervals of 40, 60, 80, and 100 % were chosen, for a constant time of 1 min. Similarly, time and amplitude conditions were used to treat solutions of XG of 1 wt.% and evaluate their influence on viscosity and how that was related to the stability of the emulsion. Increase in sonication time from 1 to 4 min led to a significant oil droplet size decrease from 1.14 to 0.89 μm (median droplet diameter). The viscosity of emulsions and XG solutions was highly influenced and considerably decreased with sonication time applied. At those conditions, an increase of backscattering was observed from 58.9 to 72.7 % after 10 days of storage, meaning that more stable emulsions, thinner and of smaller oil droplet size were produced. A similar trend was observed when the amplitude was increased, but droplet size and creaming were always greater than those noticed by changing the sonication time. However, the rate of viscosity, droplet size, and stability change was greater by increasing the amplitude rather than by changing the sonication time.     

添加玉米低聚肽的紫苏籽油乳状液及其微胶囊的制备

为制备含玉米低聚肽的紫苏籽油微胶囊,选择阿拉伯胶、可溶性大豆多糖、辛烯基琥珀酸淀粉钠（HI-CAP 100）、酪蛋白酸钠和大豆分离蛋白5 种乳化剂,并添加不同质量分数的玉米低聚肽制备紫苏籽油乳状液,筛选出制备紫苏籽油乳状液的最适乳化剂及最佳的玉米低聚肽添加比例;进而采用喷雾干燥法制备高载油量的玉米低聚肽紫苏籽油微胶囊,筛选和评价高载油量玉米低聚肽紫苏籽油微胶囊的壁材。结果显示：HI-CAP 100制备的紫苏籽油乳状液的液滴粒径主要分布在0.1～2 μm之间,并且玉米低聚肽添加量为5%时,乳状液的不稳定性指数为0.275,粒径为（0.76±0.02）μm;以HI-CAP 100为壁材经喷雾干燥制成的目标微胶囊（载油量≥50%）表面油含量为3%,表明HI-CAP 100对紫苏籽油的包埋效果较好,并且微胶囊粒径分布均匀,表面较光滑适合作为高载油量玉米低聚肽紫苏籽油微胶囊的壁材;通过加速贮藏实验证明玉米低聚肽与茶多酚棕榈酸酯复配,能提高紫苏籽油微胶囊的抗氧化性。     

Emulsifying Effects of Food Macromolecules In Presence of Ethanol

The influence on droplet size of ethanol present during homogenization was investigated for emulsions stabilized by macromolecular emulsifiers: sodium caseinate, whey protein isolate, gelatin and gum arabic. Emulsions produced with polysaccharide gum arabic had increasing droplet size as ethanol concentration increased, in contrast to the protein-stabilized emulsions which had decreasing droplet size (up to 20 % ethanol for gelatin and 30 % ethanol for the milk proteins), followed by increasing droplet size with increasing ethanol concentration. Interfacial tension measurements indicated that the emulsifying property of the macromolecules depended on adsorption at the oil-water/alcohol interface during emulsification.     

葡萄籽油微胶囊的制备及氧化稳定性研究

研究了葡萄籽油微胶囊的制备工艺及其氧化稳定性,以葡萄籽油为芯材,阿拉伯胶与麦芽糊精为壁材,在复合乳化剂的作用下进行乳化,以喷雾干燥法得到微胶囊产品并测定其氧化稳定性。研究表明阿拉伯胶与麦芽糊精重量比为3∶1,乳化剂浓度为10%,芯壁比为1∶2,温度为45℃,均质速度为12000r/min,乳化时间为12 min时制备得到稳定的葡萄籽油乳液,在进风温度180℃、出口温度80℃、进料速率5mL/min条件下喷雾干燥得到葡萄籽油微胶囊,葡萄籽油微胶囊化效率达到72.56%,60℃条件下贮藏葡萄籽油微胶囊的氧化速率明显降低,贮存性能和抗氧化性显著提高。     

Cross-linking proteins by laccase: Effects on the droplet size and rheology of emulsions stabilized by sodium caseinate

The aim of this work was to evaluate the influence of laccase and ferulic acid on the characteristics of oil-in-water emulsions stabilized by sodium caseinate at different pH (3, 5 and 7). Emulsions were prepared by high pressure homogenization of soybean oil with sodium caseinate solution containing varied concentrations of laccase (0, 1 and 5 mg/mL) and ferulic acid (5 and 10 mM). Laccase treatment and pH exerted a strong influence on the properties with a consequent effect on stability, structure and rheology of emulsions stabilized by Na-caseinate. At pH 7, O/W emulsions were kinetically stable due to the negative protein charge which enabled electrostatic repulsion between oil droplets resulting in an emulsion with small droplet size, low viscosity, pseudoplasticity and viscoelastic properties. The laccase treatment led to emulsions showing shear-thinning behavior as a result of a more structured system. O/W emulsions at pH 5 and 3 showed phase separation due to the proximity to protein pI, but the laccase treatment improved their stability of emulsions especially at pH 3. At pH 3, the addition of ferulic acid and laccase produced emulsions with larger droplet size but with narrower droplet size distribution, increased viscosity, pseudoplasticity and viscoelastic properties (gel-like behavior). Comparing laccase treatments, the combined addition of laccase and ferulic acid generally produced emulsions with lower stability (pH 5), larger droplet size (pH 3, 5 and 7) and higher pseudoplasticity (pH 5 and 7) than emulsion with only ferulic acid. The results suggested that the cross-linking of proteins by laccase and ferulic acid improved protein emulsifying properties by changing functional mechanisms of the protein on emulsion structure and rheology, showing that sodium caseinate can be successfully used in acid products when treated with laccase.     

Microencapsulation of walnut oil by spray drying: Effects of wall material and drying conditions on physicochemical properties of microcapsules

In this study, the effects of wall material formula and spray drying conditions on physicochemical properties of walnut oil microcapsules were investigated. Three different wall materials including skim milk powder (SMP), SMP + Tween 80, and SMP + maltodextrin were used for emulsion preparation. The prepared emulsions were analyzed for droplet size and stability. The emulsions were then dried in a pilot-scale spray dryer equipped with a two-fluid nozzle at different inlet drying air temperatures and feed atomization pressures in order to determine the optimal drying conditions for maximizing the microencapsulation efficiency. The microencapsulation efficiency, particle size distribution, sphericity, moisture content, bulk density, and morphology of produced microcapsules were also measured experimentally. In addition, the microcapsules with the highest microencapsulation efficiency obtained from each wall material were subjected to surface coverage of oil test using electron spectroscopy for chemical analysis (ESCA) after 60 days of storage at room temperature. The emulsion prepared using SMP and Tween 80 combination as wall material resulted in the highest microencapsulation efficiency (91.01%) at drying air temperature of 180 °C and feed atomization pressure of 3 bar. The lowest surface coverage of oil was also observed for microcapsules covered by SMP and Tween 80 combination. Scanning electron microscopy (SEM) observations showed almost no cracks or fissures on the surface of microcapsules produced using SMP and Tween 80 combination at the optimal drying condition.Industrial relevanceWalnut oil contains highly valuable constituents such as essential fatty acids, tocopherols, and phytosterols. However, a direct application of this functional oil in processed foods is problematic due to its low solubility and susceptibility to oxidation. These issues could be greatly overcome by using microencapsulation technology. Nowadays, this technology has received an increasing attention in food and pharmaceutical industries due to its unique features in protecting the functionality of ingredients. Spray drying technology is one of the most frequently used techniques for this aim. However, comprehensive studies need to be carried out in order to determine suitable operational conditions of spray drying system for improving physicochemical properties of finished powder.     

Interfacial characteristics and microchannel emulsification of oleuropein-containing triglyceride oil–water systems

This study investigated the adsorption characteristics of olive leaf water extract and its major phenolic compound, oleuropein, at the triglyceride oil–water interface. We also investigated the preparation characteristics of food-grade triglyceride oil-in-water (O/W) emulsions stabilized by oleuropein using microchannel (MC) emulsification. Refined soybean oil, extra virgin olive oil, refined olive oil, and medium-chain triacylglyceride (MCT) oil were used as triglyceride oils. Both olive leaf extract (OLE) and highly purified oleuropein had a pronounced ability to decrease the interfacial tension at the refined soybean oil–water interface. The packing of oleuropein molecules at the triglyceride oil–water interface was estimated on the basis of their surface excess concentration and area occupied per molecule, determined from the Gibbs adsorption equation. MC emulsification was performed using a silicon grooved MC array plate (model CMS6-2). The continuous aqueous phase contained 0.6 wt.% of oleuropein. Monodisperse, oleuropein-stabilized O/W emulsions with an average droplet diameter of 25 μm and coefficient of variation (CV) of < 5% were produced in all systems, except the MCT oil-containing system, even in the absence of a cross-flowing continuous phase. This successful MC emulsification was observed without droplet coalescence for 15 h of continuous operation. Our findings demonstrate that the use of oleuropein, which has an interfacial activity, is capable of producing monodisperse O/W emulsions using MC emulsification and stabilizing the generated oil droplets when appropriate types of triglyceride oils are used.     

Characterization of Chemically and Thermally Treated Oil‐in‐Water Heteroaggregates and Comparison to Conventional Emulsions

Heteroaggregated oil‐in‐water (O/W) emulsions formed by targeted combination of oppositely charged emulsion droplets were proposed to be used for the modulation of physical properties of food systems, ideally achieving the formation of a particulate 3‐dimensional network at comparably low‐fat content. In this study, rheological properties of Quillaja saponins (QS), sugar beet pectin (SBP), and whey protein isolate (WPI) stabilized conventional and heteroaggregated O/W emulsions at oil contents of 10% to 60% (w/w) were investigated. Selected systems having an oil content of 30% (w/w) and different particle sizes (d₄₃ ≤ 1.1 or ≥16.7 μm) were additionally subjected to chemical (genipin or glutaraldehyde) and thermal treatments, aiming to increase network stability. Subsequently, their rheological properties and stability were assessed. Yield stresses (τ₀) of both conventional and heteroaggregated O/W emulsions were found to depend on emulsifier type, oil content, and initial droplet size. For conventional emulsions, high yield stresses were only observed for SBP‐based emulsions (τ₀,_SBP approximately 157 Pa). Highest yield stresses of heteroaggregates were observed when using small droplets stabilized by SBP/WPI (approximately 15.4 Pa), being higher than those of QS/WPI (approximately 1.6 Pa). Subsequent treatments led to significant alterations in rheological properties for SBP/WPI systems, with yield stresses increasing 29‐fold (glutaraldehyde) and 2‐fold (thermal treatment) compared to untreated heteroaggregates, thereby surpassing yield stresses of similarly treated conventional SBP emulsions. Genipin‐driven treatments proved to be ineffective. Results should be of interest to food manufacturers wishing to design viscoelastic food emulsion based systems at lower oil droplet contents.     

Temperature and pH as factors influencing droplet size distribution and linear viscoelasticity of O/W emulsions stabilised by soy and gluten proteins

The influence of pH and two post-emulsification treatments (pH modification and thermal cycles) over linear dynamic viscoelasticity and droplet size distribution, DSD, of O/W emulsions (75% oil) stabilized either by soy protein isolate, SPI, or wheat gluten, WG were studied in the present work. Rheological properties and droplet size of fresh emulsions showed an important dependence on pH as a consequence of the role of electrostatic interactions, not being possible to obtain a stable emulsion for pH values close to the protein isoelectric point, pI, (4–5 for SPI and 6 for WG). In order to overcome this inconvenient, an alternative emulsification procedure, basically consisting in a modification of pH after emulsification (indirect emulsification), was successfully developed. Emulsions obtained after this post-emulsification treatment, showed higher elastic (G′) and loss (G″) moduli and also larger oil droplets than fresh emulsions prepared at the same pH. Moreover, the application of upward/downward temperature cycles from 20 to 70 °C to emulsions directly prepared at a pH yielded to significantly higher values of the rheological functions when compared to those found for fresh emulsions. Accordingly, both post-emulsification treatments lead to apparent enhancements in emulsion rheology and microstructure, which is indicative of a good potential to improve long-term emulsion stability.