Potential of bagasse obtained using hydrothermal liquefaction pre-treatment as a natural emulsifier

Bagasse, a by-product from raw sugar factories, is conventionally burned for energy production. In this study, bagasse extracts from hydrothermal liquefaction (HTL) treatment (160 °C, 1 MPa and 30 min) with a carbohydrate content of 510.3 mg g⁻¹ and 0.5 mg g⁻¹ of total phenols were applied as emulsifiers in oil-in-water (O/W) emulsions. Bagasse extracts from HTL (0.5–4 wt%) lowered the interfacial tension between oil–water interphase from 19.8 to 14.0 mN m⁻¹, owing possibly to the surface-active hydrophilic carbohydrate-hydrophobic lignin complexes in the extracts (lignin content: 7.1% w/w). Emulsions stabilised by bagasse extracts from HTL with average droplet size, d_av of 0.79 μm were comparable with gum arabic (GA), d_av of 2.24 μm after 11 days at 25 °C. Bagasse extracts containing biopolymers have the potential for industrial applications involving emulsion systems; therefore, HTL treatment of bagasse without any solvents can be regarded as an effective tool for producing natural emulsifiers.     

乳状液成分对O/W乳状液性质的影响

采用单因素实验设计,通过机械搅拌方法制备O/W乳状液。通过乳状液的离心稳定性、粘度和乳状液的显微结构,研究不同HLB值的复合乳化剂及含量、脱脂乳粉溶液的浓度以及油和水比例对乳状液性质的影响,最终确定较佳的乳状液成分。实验结果表明:当以Span-80和Tween-80为复合乳化剂,其HLB值为9.6、复合乳化剂含量为16%(w/w)、脱脂乳粉溶液浓度为25%(w/v)、油与水比为1∶1(w/w)时,可以获得状态较好的乳状液,此时乳状液的离心稳定性最高,可以达到97.5%。     

Stability of Lycopene Emulsions in Food Systems

ABSTRACT The chemical stability of lycopene and the physical stability of lycopene emulsions diluted in 3 different food systems (skimmed milk, orange juice, and water as control) were studied. In these investigations, 3 different emulsifiers were used. It was found that lycopene stability strongly depends on the food system. In orange juice, lycopene is particularly stable. The emulsifiers used have only little influence on the stability of lycopene. Emulsions with α-tocopherol as an additional antioxidant showed a good lycopene stability in all food systems. Coalescence of oil droplets was not observed in any of the food systems investigated. Keywords: lycopene, stability, food systems     

Utilizing high-pressure homogenization for the production of fermented plant-protein yogurt alternatives with low and high oil content using potato protein isolate as a model

The potential of high-pressure homogenization (HPH) to allow the production of a fermented potato protein isolate-based yogurt alternative with low and high oil concentration was investigated. The yogurt alternatives containing different oil concentrations (1.5%, 3%, and 10%) were obtained by inoculating the homogenized (0.1 MPa, 30 MPa, and 200 MPa) emulsions. HPH reduced emulsion particle size (all oil levels) compared to the non-homogenized samples (0.1 MPa). The overall emulsion whiteness index increased after HPH treatment while the highest value was obtained for 200 MPa 10% oil, 76.01 ± 0.50, compared to 65.33 ± 2.05 obtained for 0.1 MPa 10% oil. The creaming velocity was decreased by HPH, e.g., for 3% oil from 10.70 ± 0.11 (0.1 MPa) to 0.59 ± 0.04 after 200 MPa. Microscopic images of gels from HPH treated emulsions revealed smaller oil droplets and narrower component distribution. This study further highlights the possibility of HPH technology to produce plant-protein-based yogurt alternatives with different oil concentrations.Industrial relevanceIn recent years, the food industry has changed rapidly and has faced new consumer demands and global food trends. Consumers pay attention to food and its effect on their health, and the popularity of dairy alternatives with reduced-oil and, on the other hand, Greek-style yogurt analogs has grown. (Ultra) high-pressure homogenization ((U)HPH) is a continuously emerging technology that can potentially provide simultaneous homogenization and microbial inactivation and induce changes in solution physicochemical properties such as emulsion stabilization mainly by significantly reducing oil droplet size and improving interactions between emulsifiers and oil phase. By utilizing HPH, plant-based yogurt alternatives can be formed with a wide range of oil concentrations and similar texture profiles and water holding capacity, free of additional stabilizers and artificial emulsifiers. The results of this bottom-up approach study could be of great importance for considering the potential for scaling-up and future implementation of (U)HPH in the food industry to produce plant-based milk and yogurt alternatives with low and high oil content, having a clean label.     

Influence of enzymatic hydrolysis,pH and storage temperature on the emulsifying properties of canola protein isolate and hydrolysates

The aim of this work was to enhance emulsification properties of canola proteins through enzymatic proteolysis and pH variaton. Canola protein isolate (CPI) and hydrolysates (CPHs) were used to form emulsions at pH 4.0, 7.0 and 9.0 followed by storage at 4 or 25 °C for 7 days. Controlled enzymatic hydrolysis led to increased peptide bond cleavage with time (0.23 g/100 g in CPI to 7.18 g/100 g after 24‐h Alcalase hydrolysis). Generally, oil droplet sizes were smaller for emulsions made at pH 9.0, which suggest better quality than those made at pH 4.0 and 7.0. Trypsin hydrolysate emulsions were the most physically stable at pH 7.0 and 9.0; in contrast, the pepsin hydrolysate emulsions were unstable at all conditions. The results suggest that selective enzymatic hydrolysis could play an important role in enhancing successful incorporation of canola proteins and peptides into food systems as protein emulsifiers.     

Influence of Surfactants on the Rheological Behavior of Starch/Gelatin Gels and Gel-Emulsions

Thixotropic behavior of mixed 8% starch/gelatin gels and gel-emulsions (8% of the sunflower oil dispersed in the starch/gelatin gel), prepared with the addition of different emulsifiers, by means of the rotational viscometer with coaxial cylinders, has been investigated. Different emulsifiers (Na-dodecyl sulfate, cetyl alcohol, mono- and diglycerides of fatty acids and alkyl polyglycolethers) were applied before (at 40°C) and after (at 96°C) gelatinization of the starch. Thixotropic properties, i.e. the coefficients of thixotropy of gels and emulsions were determined by the thixotropic loop method. Samples were taken in different time intervals (up to 72 h), in order to investigate the ageing effects. Very stable gels and gel emulsions (containing carbohydrate, protein and fatty component), with high aging stability can be obtained.     

High-intensity ultrasound assisted-emulsification using ionic liquids as novel naturally-derived emulsifiers for food industry applications

Over the last decade, conscious food consumption has been revolutionizing the food industry. The search for additives that meet concepts of naturalness, healthiness and sustainability represents one of the major challenges in food industry. The development of emulsifiers in the ionic liquid (IL) form using compounds that can be obtained from natural sources to replace conventional ones is a promising approach. In this work, we have reported the application of bio-based ILs derived from fatty acids (FAs) and choline (Ch) as novel emulsifiers to produce potential food-grade oil-in-water emulsions by pre-mixing (PM) or PM followed by high-intensity ultrasound (HIUS)-assisted process (PM + U). The effects of the type of IL, considering molecular structures of FAs (C₁₈OOH or C_18:1OOH) and vegetable oil concentration (30:70 or 70:30, oil:water ratio) to form and stabilize emulsions were evaluated. The study was focused on the following aspects: synthesis and characterization of ILs, and kinetic stability, droplet size and size distribution, optical microscopy, viscosity profile and rheological behavior of the emulsions. ILs presented high emulsifier ability, since some emulsions were stable after storage time of at least 30 days, being such stability related to the type of IL, oil concentration and emulsifying process. The observed behavior was associated to lower droplet size and/or emulsion viscosity. [Ch][C₁₈OO] presented higher emulsifier ability than [Ch][C_18:1OO], and this behavior was more evident at higher oil concentration. Emulsions obtained by PM presented phase separation after their preparation, whereas most of those prepared by PM + U were visually stable, being those containing higher oil concentration the formulations that presented higher viscoelasticity, with a gel like behavior. Therefore, bio-based ILs have promising application potential as emulsifiers, and their use to obtain high stable emulsions can be enhanced by using the HIUS technique.     

Effects of bacteriostatic emulsifiers on stability of milk-based emulsions

For milk-based emulsion products such as canned coffee or tea, the addition of bacteriostatic emulsifiers is necessary to inhibiting the growth of heat-resistant sporeformers. Since bacteriostatic emulsifiers often cause the destabilization of emulsions, other type of emulsifiers, such as stability-enhancing ones, are necessary for the long-term stability of emulsions. Four milk-based emulsions were prepared from powdered milk combined with several types of emulsifiers. The long-term stability of emulsions, which was detected by the occurrence of a creaming layer after 3 months of storage, differed according to the composition of emulsifiers. To understand the reason for the differences in the stability of emulsions, particle size, distribution, ζ-potential, and the amount of proteins and phospholipids present in the cream layer (separated oil droplets) in the emulsions were measured. Only the amount of proteins adsorbed onto oil droplets was found to be closely related to the difference in emulsion stability, that is, the more proteins adsorbed, the higher the emulsion stability. SDS–PAGE analyses revealed that κ-casein and β-lactoglobulin play an important role in emulsion stability by adsorbing onto the oil droplet surface.     

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.     

Effect of emulsifier type on sensory properties of oil-in-water emulsions

This work investigates the fundamental properties of emulsifiers that may contribute to the fat-associated sensory attributes of emulsions. Model oil-in-water emulsions were prepared with 0, 12, 24, 36 and 48% oil and emulsified with seven different emulsifiers; two proteins; sodium caseinate and whey protein, and five different sucrose esters. Emulsions were rated for perceived ‘fat content’, ‘creaminess’ and ‘thickness’ on nine-point category scales. Instrumental measurements of particle size, viscosity, thin film drainage, surface dilational modulus and interfacial tension were made. The sensory results indicate significant main and interactive effects of fat level and emulsifier type. At higher fat levels, emulsions prepared with sodium caseinate and whey protein emulsifiers had higher viscosities and higher sensory scores than those prepared with the sucrose esters. Results indicate that emulsifier type has a significant effect on the sensory properties of oil-in-water emulsions, and relationships between instrumental and sensory measures suggest that this may be due to the interfacial properties of emulsifiers at the oil–water interface. © 1998 SCI.     

单、双脂肪酸甘油酯(亚麻酸)乳液的制备及特性研究

针对单、双脂肪酸甘油酯（亚麻酸）极易氧化的特点,该研究以乳清浓缩蛋白（WPC）、大豆分离蛋白（SPI）、酪蛋白酸钠（SC）和吐温80（T80）为乳化剂制备乳液,考察乳化剂类型对乳液的理化性质、氧化稳定性和消化特性的影响。结果表明,乳液均具有较小的粒径（131.97~224.87 nm）,且在两周贮藏期内保持稳定。乳液包载能够提高单、双脂肪酸甘油酯（亚麻酸）的氧化稳定性,相比T80（过氧化值为377.40 mmol/kg）,蛋白质对油脂的氧化保护效果更好,其中SPI稳定的乳液过氧化值最低为197.73 mmol/kg。体外模拟消化试验表明,乳化剂类型对游离脂肪酸的释放影响较小,但蛋白稳定的乳液在胃消化阶段更容易发生液滴聚集;亚麻籽油的脂质水解程度最低为23.93%,而单、双脂肪酸甘油酯（亚麻酸）的初始消化速度更快,最终脂解程度更高（46.33%）。因此,蛋白质乳液能有效提高单、双脂肪酸甘油酯（亚麻酸）的氧化稳定性,且单、双脂肪酸甘油酯（亚麻酸）相比亚麻籽油具有更好的消化效率,有望替代亚麻籽油作为人体亚麻酸的食物来源。     

Iron‐mediated lipid oxidation in 70% fish oil‐in‐water emulsions: effect of emulsifier type and pH

The objective of this study was to investigate the protective effect of five different emulsifiers on iron‐mediated lipid oxidation in 70% fish oil‐in‐water emulsions. The emulsifiers were either based on protein (whey protein isolate and sodium caseinate) or based on phospholipid (soy lecithin and two milk phospholipids with different phospholipid contents, MPL20 and MPL75). Lipid oxidation was studied at pH 4.5 and 7.0, and results were compared to lipid oxidation in neat fish oil. Results showed that all emulsions oxidised more than neat oil. Furthermore, emulsions prepared with proteins oxidised more at low pH than at high pH, and casein emulsions oxidised the least (Peroxide value (PV) at day 7 was 0.5–0.7 meq kg^?1). Among emulsions prepared with phospholipids, emulsions with MPL75 were the most oxidised followed by emulsions prepared with lecithin and MPL20. Thus, PV in MPL75 emulsions was 5.0–5.5 meq kg^?1 at day 7 compared with 0.9–1.9 meq kg^?1 in MPL20 emulsions.     

Emulsification by the phase inversion temperature method: the role of self-bodying agents and the influence of oil polarity

Oil-in-water emulsions stabilized with nonionic emulsifiers change to water-in-oil emulsions as the temperature rises when the hydrophilic and lipophilic properties of the mixed emulsifier are just balanced. Preparation above the phase inversion temperature followed by rapid cooling yields emulsions that exhibit very fine droplet size and extreme long-term stability. Cosmetic emulsions were prepared by this phase inversion temperature (PIT) method using typical raw materials such as polar oils, e.g. decyl oleate, 2-octyl dodecanol or isopropyl myristate, and nonionic emulsifiers, e.g. ceteareth-12 or polyoxyethylene eicosyl/docosyl ether combined with cetostearyl alcohol as a co-emulsifier. The phase inversion temperature was measured as a function of the oil polarity and the concentration of mixed emulsifier. The relationship between phase inversion temperature, droplet size and emulsion stability was investigated. In addition, self-bodying agents such as cetostearyl alcohol or monoglycerides were added to these thin, fine disperse emulsions to adjust the consistency. The influence of these ingredients on phase inversion temperature, droplet size, yield value and emulsion stability was studied.     

Quality control of commercial quillaja (Quillaja saponaria Molina) extracts by reverse phase HPLC

Saponin‐rich extracts of the Chilean indigenous tree Quillaja saponaria Molina are widely used as natural foaming agents in foods and beverages, food emulsifiers, photographic emulsions, vaccine adjuvants, etc. However, with the exception of the vaccine industry, saponin concentration is not adequately quantified. Normally, the quality and price of the extracts are determined using simple foam tests. This may not be adequate, since similar foam levels can be obtained by blending quillaja extracts with other low‐cost saponin sources (eg Yucca shidigera extracts). Also, many products are diluted with high amounts of carriers, reducing significantly their saponin concentration. To overcome these problems and standardise the quality of commercial extracts, the use of reverse phase HPLC techniques is explored. It is shown that RP‐HPLC yields consistent and repetitive results and can be easily implemented to control the quality of quillaja extracts. Commercial non‐refined extracts contain 190–200 g saponins kg⁻¹ solids, while semi‐refined extracts contain 750–800 g saponins kg⁻¹ solids. Also, extracts derived from quillaja bark (traditional raw material) and whole quillaja wood (novel ecological production method) have similar saponin composition and concentration. © 2000 Society of Chemical Industry     

Emulsifying properties of gum kondagogu (Cochlospermum gossypium), a natural biopolymer

BACKGROUND: Natural polymers are widely used as emulsifying agents in the food and pharmaceutical industries because of their low cost, biocompatibility and non‐toxic nature. In the present study, emulsifying properties of the novel natural biopolymer gum kondagogu (GKG) were investigated. GKG solutions of different concentrations (0.1–0.6% w/v) were prepared in water and emulsified with liquid paraffin oil (40% v/v) in a high‐speed homogeniser. Flow properties of the emulsions were measured using a rheometer. Emulsion stability and droplet size distribution were determined by visual observation, photomicrography and laser‐scattering particle size distribution analysis. RESULTS: The emulsions prepared with GKG showed pseudoplastic behaviour. The size of oil droplets and the viscosity of emulsions at concentrations of 0.4–0.6% w/v showed little change over time (up to 30 days), indicating that the emulsions were stable. Measurements of the zeta potential of emulsions adjusted to different pH, with and without added electrolyte, showed that the stabilisation of emulsions with GKG was due to mutual repulsion between electrical double layers of particles and adsorption of macromolecules on oil droplets. CONCLUSION: The results of this experimental investigation show that GKG is a good emulsifying agent even at low concentrations, with many potential applications in the food and pharmaceutical industries. Copyright © 2009 Society of Chemical Industry     

The effect of emulsifier type and oil inclusion on stress-related gene expression of Salmonella typhimurium in oil-in-water emulsion

Salmonella has been associated with numerous outbreaks from contaminated food products, including emulsions. Emulsions are influenced by emulsifier type and oil presence, which can have varying degrees of stress or protection on bacteria. Although our previous research has shown that emulsifier solutions, rather than emulsions, provide a protective effect on Salmonella typhimurium after thermal treatment, the underlying mechanism remains unclear. This study selected S. typhimurium as the model microorganism and utilized the same emulsifiers (Tween 20, Tween 80, Triton X-100) to create emulsifier solutions and emulsions with the same oil fraction (60% (v/v)) to examine their effect on the expression of nine selected genes (rpoE, rpoH, otsB, proV, fadA, fabA, dnaK, ibpA, ompC) associated with stress response. Specifically, the study observed variations in gene expression under normal and thermal stress at 55°C. After 20-h incubation, Triton X-100 emulsion caused an upregulation of stress-related genes, rpoE, otsB, and fabA, suggesting stressful environment. After thermal treatment, S. typhimurium in Triton X-100 solution showed a longer 5-log reduction time with increased proV and decreased fabA and ompC expression, suggesting enhanced thermal protection compared to its emulsion. Conversely, Tween 80 solution increased fabA and ompC expression, indicating greater membrane fluidity and passive diffusion, potentially reducing thermal resistance. However, according to the upregulation of ibpA, this effect was likely mitigated by the overproduction of heat shock proteins. Notably, Triton X-100 environments exhibited the most significant gene expression changes after heat treatment, whereas Tween 80 without oil was the most inhospitable for bacterial survival. These findings inform bacterial responses under various conditions, aiding food safety strategies.     

Functional properties of processed Australian wattle (Acacia victoriae Bentham) seed extracts

Functional properties of water extracts from processed prickly wattle (Acacia victoriae Bentham) seed flours were compared to those of raw flours and an ammonium sulphate precipitate (ASP) containing >77% protein. All extracts formed stable 20% and 50% (v/v) oil-in-water emulsions at concentrations between 1% and 5% (w/v) but the emulsions formed from processed flour at low extract concentrations destabilized by oiling off within 7 days at 25 °C. Comparatively, emulsions formed with 5% raw and processed extracts creamed or broke reversibly. Conversely, ASP-stabilized emulsions were very stable at all concentrations and conditions in this study. However, all extracts and ASP had poor foaming capacity and did not gel even at up to 10% solids concentration. The results indicated that processing of wattle seeds for flavour enhancement or destruction of anti-nutrients led to poorer functionality. The excellent emulsifying and emulsion stabilization properties of ASP could potentially be exploited in processed foods.     

Antioxidant Properties of Aqueous Extract of Roasted Hulled Barley in Bulk Oil or Oil‐in‐Water Emulsion Matrix

Antioxidant properties of the aqueous extracts of hulled barley (Hordeum vulgare L.) that had been roasted at 210 °C for 20 min were determined in bulk oil and oil‐in‐water (O/W) emulsions. Bulk oils were heated at 60, 100, and 180 °C, and O/W emulsions were oxidized under riboflavin photosensitization. The content of phenolic compounds was analyzed by high‐performance liquid chromatography, and in vitro antioxidant assays were also conducted. The major phenolics contained in the aqueous extract of roasted hulled barley (AERB) were p‐coumaric, ferulic, protocatechuic, chlorogenic, 4‐hydroxybenzoic, and vanillic acids. Depending on the concentration and oxidation temperature, AERB had antioxidant or prooxidant properties in bulk oil. At 60 °C, AERB at a concentration of 0.5% acted as a prooxidant, whereas at 1.0% it acted as an antioxidant. At 100 °C, AERB acted as an antioxidant irrespective of concentration. In 180 °C conditions, 0.5% AERB acted as a prooxidant, whereas other concentrations of AERB acted as antioxidants. In the case of riboflavin photosensitized O/W emulsions, AERB showed antioxidant properties irrespective of concentration. Antioxidant abilities of AERB are affected by the food matrix, including bulk oil and O/W emulsions, and concentrations of AERB, even though diverse phenolic compounds may display high antioxidant properties in in vitro assays.     

Emulsifying properties of protein–pectin complexes and their use in oil-containing foodstuffs

The emulsifying properties of proteins have been well studied as they are important for the preparation of creams, mayonnaises and other oil/fat-containing foodstuffs. The emulsifying action of a protein is not always sufficient to obtain stable emulsions of good quality. The use of chemical stabilisers in the food industry is not desirable. One of the best ways to improve the quality of emulsions and to produce emulsions with high nutritive value is to use protein-polysaccharide complexes as emulsifiers. Varying the protein-polysaccharide ratio in the complex, and also the kind of the polymers, would vary the quality and the nutritional value of the foodstuff. Four non-conventional protein preparations were tested as emulsifiers and their emulsifying properties were improved by the addition of pectin. This makes it possible to create new foodstuffs with low oil content and high nutritional value.     

Role of emulsifier layer,antioxidants and radical initiators in the oxidation of olive oil-in-water emulsions

Lipid oxidation in oil-in-water (O/W) emulsions is largely affected by the properties of the interfacial layer surrounding the oil droplets. In this work, the effect of the emulsifier layer structure, presence of both hydrophilic and lipophilic antioxidants and radical initiators on the development of lipid oxidation in olive oil-in-water emulsions was investigated. The olive oil-in-water emulsion is a suitable model of low fat food emulsions. The rationale of the work was to study the role of the interfacial layer when both the antioxidants and the radical initiators came from the two different emulsion compartments. Emulsions were prepared by using food grade emulsifiers of the Tween series (polyoxyethylene sorbitan esters) in the water phase and Span 80 (sorbitan monoleate) in the oil phase. The properties of the interfacial layer were changed by using Tween 20, Tween 60, Tween 80, which have different hydrophobic tails. These systems were oxidized by means of both hydrophilic (AAPH (2,2′-azobis,2-methyl-propanimidamide dihydrochloride), AIPH (2,2′-azobis[2-(2-imidazolin-2-yl) propane] dihydrochloride) and lipophilic (AMVN (2,2′-azobis(2,4-dimethylvaleronitrile)) radical initiators at 40 °C. A continuous fluorescent method based on the front face technique allowed us to follow directly the development of oxidation in the whole emulsion. The combination Tween 80/Span 80 produced an interfacial layer more resistant to radical attack. Moreover, a polar paradox was verified also for radical initiators, while the results suggest that the best way to protect emulsions is to use a combination of antioxidants in both phases, to promote a synergy and the regeneration of antioxidants mediated by the interfacial layer.