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Mechanical Regimes in Gelatin and Gellan Gum Bigels: Structure-Function Relationships and Dual Delivery of Carob
Alicia Gutiérrez1, Susana Cofrades1, Arancha Saiz1
1Institute of Food Science, Technology and Nutrition (ICTAN-CSIC), C/José Antonio Novais 6, 28040 Madrid, Spain.
Abstract:
Bigels (BGs) were formulated using gelatin (GA) or gellan gum (GG) hydrogels (HGs) combined with beeswax-structured oleogels (OGs). Carob fruit extracts-an inositol-rich fraction (I-CFE) and a polyphenol-rich fraction (P-CFE)-were incorporated into the HG and OG phases, respectively, to enable dual delivery. The effects of composition on rheological, textural, thermal, color, and stability properties were evaluated at HG/OG ratios of 70/30, 60/40, and 50/50. GG-based BGs formed rigid, coherent, and crystal-reinforced networks, exhibiting the highest oscillatory stiffness and complex viscosity. GA-based BGs developed softer, more deformable, and viscous structures, with mechanical behavior strongly governed by damping and water content. Increasing OG content reinforced GG BGs through beeswax-crystal integration, whereas in GA it increased oscillatory stiffness but weakened the cohesive, viscous, and recoverable characteristics of the protein network. Categorical principal component analysis (CATPCA) revealed two mechanical domains: a GA-associated regime dominated by viscosity, penetration resistance, and loss factor (tan δ), and a GG-associated regime governed by elastic stiffness. Correlations confirmed tan δmax as a marker of structural fragility in GA, while stiffness parameters dominated GG behavior. Melting points remained within 53-54 °C, and all BGs showed excellent physical stability. Overall, GA and GG provide complementary design spaces, offering a mechanistic basis for the rational design of BGs with controlled structural and functional properties.
