ArticleSmall (Weinheim an der Bergstrasse, Germany)2026
Interfacial-Bulk Synergistic Stabilization of Dual-Network Emulsion Gels by Protein-Polysaccharide Ternary Biopolymer System.
Article in Small (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
Plant-based emulsion gels represent sustainable, biocompatible soft materials with transformative potential in food, biomedicine, and advanced manufacturing. However, a long-standing bottleneck persists in simultaneously achieving long-term colloidal stability and robust mechanical properties using exclusively natural biopolymers, severely limiting their practical deployment. Herein, we report an interfacial-bulk synergistic stabilization strategy by constructing a soy protein isolate (SPI)-konjac glucomannan (KGM)-κ-carrageenan (KC) ternary biopolymer system. We systematically elucidate that SPI dominates interfacial adsorption to form elastic interfacial films, while KGM-KC complexes construct a physically crosslinked bulk network to enhance viscosity and steric hindrance, enabling collaborative stabilization at both interface and bulk phases. Leveraging this synergy, stable high internal phase emulsions are readily fabricated. Furthermore, transglutaminase-induced covalent crosslinking of SPI interpenetrates with the KGM-KC physical network, yielding a robust dual-crosslinked emulsion gel with significantly enhanced mechanical strength, water-holding capacity, and freeze-thaw stability. Notably, the optimized gels exhibit excellent 3D printability with high shape fidelity, demonstrating great potential for personalized food manufacturing and bioactive delivery. This work provides fundamental insights into protein-polysaccharide synergistic interactions and establishes an effective strategy for engineering high-performance all-natural soft materials.
Indexed as
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.