High-pressure homogenization transformed salmon protein filament into micelle structure: Improvement on the stability and swallowing rheology of dysphagia-oriented salmon emulsion gels.

The aging population is stimulating increased demand for dysphagia-oriented foods, yet most current options are made of ultra-processed macronutrients and lack high-quality protein and ω-3 fatty acids. This study explores the use of whole salmon fillets as a myofibrillar protein source to stabilize salmon backbone oil, creating ω-3-rich emulsion gels (50-60 vol%) for dysphasia individuals. Two-step high-pressure homogenization (HPH; 50 MPa) improved emulsion texture, storage stability, and swallowability (IDDSI level 4) by reducing oil droplet size (from 20 to 2 μm) and increasing elastic modulus by 6-8 times and viscosity by more than 10 times. These emulsion gels, rich in PUFAs, support cardiovascular health. HPH altered the structure of salmon myofibrillar proteins, transforming from micro-sized filament (2.5 μm) to assembled nano-sized micelle aggregate (400 nm) through reducing α-helix structure, crystallization, particle size, and aggregation. The protein interfacial stiffness and stability were improved, thus exhibiting greater oil droplet stabilization. The study offers a compelling reference for applying HPH in producing dysphagia-oriented products.