Bigel formation through surfactant-free co-gelation-in-emulsion without thermal activation of the hydrogel: Expanding the toolbox for customizable, and food-grade fat replacers

Replacing saturated and trans fats with healthier alternatives remains a major challenge for the food industry. This study presents a simple method to fabricate food-grade bigels with improved structural and functional properties. A surfactant-free co-gelation-in-emulsion approach was applied, in which basic pullulan, sodium trimetaphosphate (STMP) solutions were emulsified with molten candelilla wax/extra virgin olive oil solutions under mild agitation. Hydro- and oleo-gelation ocurred simultaneously once emulsion was prepared, withput thermal activation of the hidrogel, directly forming the bigel. Bigels with hydrogel-to-oleogel ratios of 25:75, 50:50, and 75:25 were produced and compared with systems obtained by conventional high-shear mixing of the separately prepared hydro- and oleo-gels. Co-gelated bigels exhibited homogeneous phase distribution, solid-like rheology, and high oil-binding capacity (>80 % at 25 % hydrogel; no oil leakage at ≥50 %). When the hydrogel acted as the continuous phase (≥50 %), the systems displayed marked increases in elasticity (G′ > 6000 Pa), hardness (≈450–500 g), and swelling (up to 55 %), closely resembling pure hydrogels. In contrast, mixed bigels prepared by high shear mixing of single gels presented fragmented, heterogeneous structures with lower stability and weaker texture. FT-IR, WAXS, and confocal microscopy confirmed improved hydrogen bonding, maintenance of oleogel crystallinity, and more continuous networks in co-gelated samples. This thermally independent route of the hydriphilic domain enables the use of biopolymers with slow chemical cross-linking kinetics (such as pullulan-STMP) and yields bigels that are more homogeneous, mechanically stronger, and oil-retentive. Overall, the method broadens the possibilities of food-grade bigels as customizable fat replacers. • Bigels were prepared by co-gelation-in-emulsion without hydrogel thermal activation. • Method enables stable, elastic bigels as potential food-grade fat replacers. • Surfactant-free strategy broadens biopolymer use in bigel formulation. • Co-gelated bigels show higher oil retention and elasticity than mixed Systems with the same formation.

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Publication Details

Journal
Journal of Food Engineering
Published
2025-10-31
DOI
https://doi.org/10.1016/j.jfoodeng.2025.112848
Primary Topic
Food Chemistry and Fat Analysis
Type
article
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article

Bigel formation through surfactant-free co-gelation-in-emulsion without thermal activation of the hydrogel: Expanding the toolbox for customizable, and food-grade fat replacers

Esther Santamaría, C. González, Akbota Adilbekova, Alicia Maestro et al.
Journal of Food Engineering
Food Chemistry and Fat Analysis
article

Bigel formation through surfactant-free co-gelation-in-emulsion without thermal activation of the hydrogel: Expanding the toolbox for customizable, and food-grade fat replacers

Esther Santamaría, C. González, Akbota Adilbekova, Alicia Maestro, Jonathan Miras
article en

Abstract

Replacing saturated and trans fats with healthier alternatives remains a major challenge for the food industry. This study presents a simple method to fabricate food-grade bigels with improved structural and functional properties. A surfactant-free co-gelation-in-emulsion approach was applied, in which basic pullulan, sodium trimetaphosphate (STMP) solutions were emulsified with molten candelilla wax/extra virgin olive oil solutions under mild agitation. Hydro- and oleo-gelation ocurred simultaneously once emulsion was prepared, withput thermal activation of the hidrogel, directly forming the bigel. Bigels with hydrogel-to-oleogel ratios of 25:75, 50:50, and 75:25 were produced and compared with systems obtained by conventional high-shear mixing of the separately prepared hydro- and oleo-gels. Co-gelated bigels exhibited homogeneous phase distribution, solid-like rheology, and high oil-binding capacity (>80 % at 25 % hydrogel; no oil leakage at ≥50 %). When the hydrogel acted as the continuous phase (≥50 %), the systems displayed marked increases in elasticity (G′ > 6000 Pa), hardness (≈450–500 g), and swelling (up to 55 %), closely resembling pure hydrogels. In contrast, mixed bigels prepared by high shear mixing of single gels presented fragmented, heterogeneous structures with lower stability and weaker texture. FT-IR, WAXS, and confocal microscopy confirmed improved hydrogen bonding, maintenance of oleogel crystallinity, and more continuous networks in co-gelated samples. This thermally independent route of the hydriphilic domain enables the use of biopolymers with slow chemical cross-linking kinetics (such as pullulan-STMP) and yields bigels that are more homogeneous, mechanically stronger, and oil-retentive. Overall, the method broadens the possibilities of food-grade bigels as customizable fat replacers. • Bigels were prepared by co-gelation-in-emulsion without hydrogel thermal activation. • Method enables stable, elastic bigels as potential food-grade fat replacers. • Surfactant-free strategy broadens biopolymer use in bigel formulation. • Co-gelated bigels show higher oil retention and elasticity than mixed Systems with the same formation.

Journal of Food EngineeringVol. 407
Consejo Superior de Investigaciones Científicas (ES), Universitat Oberta de Catalunya (ES), Al-Farabi Kazakh National University (KZ), Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (ES), Institute of Advanced Chemistry of Catalonia (ES), Universitat de Barcelona (ES)
Openalex Percentile: Top 62%
Food Chemistry and Fat Analysis
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